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(R)-5-乙酰氧基-1-氯己烷 | 154885-34-4

中文名称
(R)-5-乙酰氧基-1-氯己烷
中文别名
——
英文名称
(R)-5-acetoxy-1-chlorohexane
英文别名
5-(R)-acetoxy-1-chlorohexane;(R)-2-acetoxy-6-chlorohexane;(R) 5-acetoxy-1-chlorohexane;[(2R)-6-chlorohexan-2-yl] acetate
(R)-5-乙酰氧基-1-氯己烷化学式
CAS
154885-34-4
化学式
C8H15ClO2
mdl
——
分子量
178.659
InChiKey
CCAJQWQPQNZYTE-SSDOTTSWSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    220 °C(lit.)
  • 密度:
    1.02 g/mL at 25 °C(lit.)
  • 闪点:
    213 °F
  • 稳定性/保质期:
    在常温常压下保持稳定,应避免与强氧化剂、碱以及活泼金属接触。

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S26
  • 危险类别码:
    R22
  • 储存条件:
    密封存储,应存放在阴凉干燥的仓库中。

SDS

SDS:cc3087319e63a3de7667d71e36db1d4c
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Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product name : (R)-5-Acetoxy-1-chlorohexane

Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
According to Regulation (EC) No1272/2008
Acute toxicity, Oral (Category 4)
Skin irritation (Category 2)
Eye irritation (Category 2)
Carcinogenicity (Category 2)
Specific target organ toxicity - single exposure (Category 3)
According to European Directive 67/548/EEC as amended.
Harmful if swallowed. Irritating to eyes, respiratory system and skin. Limited evidence of a carcinogenic effect.
Label elements
Pictogram
Signal word Warning
Hazard statement(s)
H302 Harmful if swallowed.
H315 Causes skin irritation.
H319 Causes serious eye irritation.
H335 May cause respiratory irritation.
H351 Suspected of causing cancer.
Precautionary statement(s)
P261 Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray.
P281 Use personal protective equipment as required.
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact lenses, if present and easy to do. Continue rinsing.
Hazard symbol(s)
Xn Harmful
R-phrase(s)
R22 Harmful if swallowed.
R36/37/38 Irritating to eyes, respiratory system and skin.
R40 Limited evidence of a carcinogenic effect.
S-phrase(s)
S26 In case of contact with eyes, rinse immediately with plenty of water and
seek medical advice.
S36 Wear suitable protective clothing.
Other hazards - none

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Formula : C8H15ClO2
Molecular Weight : 178,66 g/mol
CAS-No. EC-No. Index-No. Classification Concentration
5-(R)-Acetoxy-1-chlorohexane
154885-34-4 - - Acute Tox. 4; Skin Irrit. 2; Eye -
Irrit. 2; Carc. 2; STOT SE 3;
H302, H315, H319, H335,
H351
Xn, R22 - R36/37/38 - R40
For the full text of the H-Statements mentioned in this Section, see Section 16.

Section 4. FIRST AID MEASURES
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special protective equipment for fire-fighters
Wear self contained breathing apparatus for fire fighting if necessary.

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions
Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation.
Evacuate personnel to safe areas.
Environmental precautions
Prevent further leakage or spillage if safe to do so. Do not let product enter drains.
Methods and materials for containment and cleaning up
Soak up with inert absorbent material and dispose of as hazardous waste. Keep in suitable, closed
containers for disposal.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Avoid contact with skin and eyes. Avoid inhalation of vapour or mist.
Normal measures for preventive fire protection.
Conditions for safe storage
Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully
resealed and kept upright to prevent leakage. Store in cool place.

Section 8. EXPOSURE CONTROLS/PERSONAL PROTECTION
Personal protective equipment
Respiratory protection
Where risk assessment shows air-purifying respirators are appropriate use a full-face respirator with
multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to
engineering controls. If the respirator is the sole means of protection, use a full-face supplied air
respirator. Use respirators and components tested and approved under appropriate government
standards such as NIOSH (US) or CEN (EU).
Hand protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique (without
touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves
after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the
standard EN 374 derived from it.
Eye protection
Face shield and safety glasses Use equipment for eye protection tested and approved under appropriate
government standards such as NIOSH (US) or EN 166(EU).
Skin and body protection
Complete suit protecting against chemicals, The type of protective equipment must be selected according
to the concentration and amount of the dangerous substance at the specific workplace.
Hygiene measures
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at
the end of workday.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Appearance
Form liquid
Colour colourless
Safety data
pH no data available
Melting point no data available
Boiling point 220 °C - lit.
Flash point 100,6 °C - closed cup
Ignition temperature no data available
Lower explosion limit no data available
Upper explosion limit no data available
Density 1,02 g/cm3 at 25 °C
Water solubility no data available

Section 10. STABILITY AND REACTIVITY
Chemical stability
Stable under recommended storage conditions.
Conditions to avoid
no data available
Materials to avoid
Strong oxidizing agentsStrong oxidizing agents, Bases, Chemically active metals
Hazardous decomposition products
Hazardous decomposition products formed under fire conditions. - Carbon oxides, Hydrogen chloride gas

Section 11. TOXICOLOGICAL INFORMATION
Acute toxicity
no data available
Skin corrosion/irritation
no data available
Serious eye damage/eye irritation
no data available
Respiratory or skin sensitization
no data available
Germ cell mutagenicity
no data available
Carcinogenicity
Limited evidence of carcinogenicity in animal studies
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
no data available
Specific target organ toxicity - single exposure
Inhalation - May cause respiratory irritation.
Specific target organ toxicity - repeated exposure
no data available
Aspiration hazard
no data available
Potential health effects
Inhalation May be harmful if inhaled. Causes respiratory tract irritation.
Ingestion Harmful if swallowed.
Skin May be harmful if absorbed through skin. Causes skin irritation.
Eyes Causes serious eye irritation.
Signs and Symptoms of Exposure
To the best of our knowledge, the chemical, physical, and toxicological properties have not been thoroughly
investigated.
Additional Information
RTECS: Not available

Section 12. ECOLOGICAL INFORMATION
Toxicity
no data available
Persistence and degradability
no data available
Bioaccumulative potential
no data available
Mobility in soil
no data available
PBT and vPvB assessment
no data available
Other adverse effects
no data available

Section 13. DISPOSAL CONSIDERATIONS
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed professional
waste disposal service to dispose of this material.
Contaminated packaging
Dispose of as unused product.

Section 14. TRANSPORT INFORMATION
ADR/RID
Not dangerous goods
IMDG
Not dangerous goods
IATA
Not dangerous goods



SECTION 15 - REGULATORY INFORMATION
N/A


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (R)-5-乙酰氧基-1-氯己烷甲醇potassium carbonate 、 sodium iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 11.0h, 生成 (R)-6-phthalimido-2-hexanol
    参考文献:
    名称:
    环戊烯酮催化甲磺酸盐取代醇
    摘要:
    描述了环丙烯酮通过甲磺酸根离子催化醇的亲核取代,且构型反转。这项工作为Mitsunobu反应提供了另一种选择,该方法避免了使用偶氮二羧酸盐以及生成肼和氧化膦副产物。已显示此转换与一系列功能兼容。已证明环丙酮清除策略有助于纯化。
    DOI:
    10.1021/ol302970c
  • 作为产物:
    描述:
    5-(R)-acetoxy-1-hydroxyhexane 以67的产率得到(R)-5-乙酰氧基-1-氯己烷
    参考文献:
    名称:
    [EN] ASYMMETRIC SYNTHESIS OF CHIRAL SECONDARY ALCOHOLS
    [FR] SYNTHESE ASYMETRIQUE D'ALCOOLS SECONDAIRES CHIRAUX
    摘要:
    一种使用天然手性分子起始材料合成与杂环核心基团相连的对映纯手性二级醇化合物的方法,该创新性方法特别适用于大规模生产手性二级醇化合物。
    公开号:
    WO1995031450A1
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文献信息

  • TRICYCLIC FUSED XANTHINE COMPOUNDS AND THEIR USES
    申请人:Cell Therapeutics, Inc.
    公开号:US20020103211A1
    公开(公告)日:2002-08-01
    Novel tricyclic compounds are found to be useful for the treatment or prevention of symptoms or manifestations associated with diseases or disorders affected by cytokine intracellular signaling.
    发现新型三环化合物对于治疗或预防受细胞因子内部信号传导影响的疾病或疾病相关症状或表现具有益处。
  • THERAPEUTIC COMPOUNDS FOR INHIBITING INTERLEUKIN-12 SIGNALING AND METHODS FOR USING SAME
    申请人:——
    公开号:US20020028823A1
    公开(公告)日:2002-03-07
    Novel heterocyclic compounds having a six membered ring structure fused to a five membered ring structure are found to be useful for the treatment and prevention of symptoms or manifestations associated with disorders affected by Interleukin-12 (“IL-12”) intracellular signaling, such as, for example, Th1 cell-mediated disorders. The therapeutic compounds, pharmaceutically acceptable derivatives (e.g., resolved enantiomers, diastereomers, tautomers, salts and solvates thereof) or prodrugs thereof, have the following general formula: 1 Each X, Y and Z are independently selected from a member of the group consisting of C(R 3 ), N, N(R 3 ) and S. Each R 1 , R 2 and R 3 is substituted or unsubstituted and is independently selected from a member of the group consisting of hydrogen, halo, oxo, C (1-20) alkyl, C (1-20) hydroxyalkyl, C (1-20) thioalkyl, C (1-20) alkylamino, C (1-20) alkylaminoalkyl, C (1-20) aminoalkyl, C (1-20) aminoalkoxyalkenyl, C (1-20) aminoalkoxyalkynyl, C (1-20) diaminoalkyl, C (1-20) triaminoalkyl, C (1-20) tetraaminoalkyl, C (5-15) aminotrialkoxyamino, C (1-20) alkylamido, C (1-20) alkylamidoalkyl, C (1-20) amidoalkyl, C (1-20) acetamidoalkyl, C (1-20) alkenyl, C (1-20) alkynyl, C (3-8) alkoxyl, C (1-11) alkoxyalkyl, and C (1-20) dialkoxyalkyl.
    发现具有六元环结构与五元环结构融合的新型杂环化合物可用于治疗和预防与受干扰素-12(“IL-12”)细胞内信号传导影响的疾病相关的症状或表现,例如Th1细胞介导的疾病。这些治疗化合物、药学上可接受的衍生物(例如,其溶解对映体、异构体、互变异构体、盐和溶剂)或其前体具有以下一般公式:1每个X、Y和Z独立地选择自C(R3)、N、N(R3)和S所组成的成员。每个R1、R2和R3被取代或未取代,并且独立地选择自氢、卤素、氧、C(1-20)烷基、C(1-20)羟基烷基、C(1-20)硫基烷基、C(1-20)烷基氨基、C(1-20)烷基氨基烷基、C(1-20)氨基烷基、C(1-20)氨基氧基烯基、C(1-20)氨基氧基炔基、C(1-20)二氨基烷基、C(1-20)三氨基烷基、C(1-20)四氨基烷基、C(5-15)氨基三烷氧氨基、C(1-20)烷基酰胺、C(1-20)烷基酰胺烷基、C(1-20)酰胺烷基、C(1-20)乙酰胺烷基、C(1-20)烯基、C(1-20)炔基、C(3-8)烷氧基、C(1-11)烷氧基烷基和C(1-20)二烷氧基烷基。
  • Therapeutic compounds for inhibiting interleukin-12 signaling and methods for using same
    申请人:Cell Therapeutics, Inc.
    公开号:US06774130B2
    公开(公告)日:2004-08-10
    Novel heterocyclic compounds having a six membered ring structure fused to a five membered ring structure are found to be useful for the treatment and prevention of symptoms or manifestations associated with disorders affected by Interleukin-12 (“IL-12”) intracellular signaling, such as, for example, Th1 cell-mediated disorders. The therapeutic compounds, pharmaceutically acceptable derivatives (e.g., resolved enantiomers, diastereomers, tautomers, salts and solvates thereof) or prodrugs thereof, have the following general formula: Each X, Y and Z are independently selected from a member of the group consisting of C(R3), N, N(R3) and S. Each R1, R2 and R3 is substituted or unsubstituted and is independently selected from a member of the group consisting of hydrogen, halo, oxo, C(1-20)alkyl, C(1-20)hydroxyalkyl, C(1-20)thioalkyl, C(1-20)alkylamino, C(1-20)alkylaminoalkyl, C(1-20)aminoalkyl, C(1-20)aminoalkoxyalkenyl, C(1-20)aminoalkoxyalkynyl, C(1-20)diaminoalkyl, C(1-20)triaminoalkyl, C(1-20)tetraaminoalkyl, C(5-15)aminotrialkoxyamino, C(1-20)alkylamido, C(1-20)alkylamidoalkyl, C(1-20)amidoalkyl, C(1-20)acetamidoalkyl, C(1-20)alkenyl, C(1-20)alkynyl, C(3-8)alkoxyl, C(1-11)alkoxyalkyl, and C(1-20)dialkoxyalkyl.
    具有六元环结构与五元环结构融合的新颖杂环化合物被发现对治疗和预防与受白细胞介素-12(“IL-12”)细胞内信号传导受影响的疾病相关的症状或表现有用,例如Th1细胞介导的疾病。这些治疗化合物、药学上可接受的衍生物(例如,已解决的对映体、二对映体、互变异构体、盐及其溶剂)或其前药具有以下一般公式:每个X、Y和Z都独立地选自由基团中的成员,该成员包括C(R3)、N、N(R3)和S。每个R1、R2和R3都被取代或未取代,并且独立地选自由基团中的成员,该成员包括氢、卤素、氧代、C(1-20)烷基、C(1-20)羟基烷基、C(1-20)硫基烷基、C(1-20)烷基氨基、C(1-20)烷基氨基烷基、C(1-20)氨基烷基、C(1-20)氨基氧烯基、C(1-20)氨基烷氧基炔基、C(1-20)二氨基烷基、C(1-20)三氨基烷基、C(1-20)四氨基烷基、C(5-15)氨基三烷氧基氨基、C(1-20)烷基酰胺、C(1-20)烷基酰胺烷基、C(1-20)酰胺烷基、C(1-20)乙酰胺烷基、C(1-20)烯基、C(1-20)炔基、C(3-8)烷氧基、C(1-11)烷氧基烷基和C(1-20)二烷氧基烷基。
  • Therapeutic compounds for inhibiting interleukin-12 signals and method for using same
    申请人:Klein J. Peter
    公开号:US06878715B1
    公开(公告)日:2005-04-12
    Novel heterocyclic compounds having a six membered ring structure fused to a five membered ring structure are found to be useful for the treatment and prevention of symptoms or manifestations associated with disorders affected by Interleukin-12 (“IL-12”) intracellular signaling, such as, for example, Th1 cell-mediated disorders. The therapeutic compounds, pharmaceutically acceptable derivatives (e.g., resolved enantiomers, diastereomers, tautomers, salts and solvates thereof) or prodrugs thereof, have the following general formula: Each X, Y and Z are independently selected from a member of the group consisting of C(R 3 ), N, N(R 3 ) and S. Each R 1 , R 2 and R 3 is substituted or unsubstituted and is independently selected from a member of the group consisting of hydrogen, halo, oxo, C (1-20) alkyl, C (1-20) hydroxyalkyl, C (1-20) thioalkyl, C (1-20) alkylamino, C (1-20) alkylaminoalkyl, C (1-20) aminoalkyl, C (1-20) aminoalkoxyalkenyl, C (1-20) aminoalkoxyalkynyl, C (1-20) diaminoalkyl, C (1-20) triaminoalkyl, C (1-20) tetraaminoalkyl, C (5-15) aminotrialkoxyamino, C (1-20) alkylamido, C (1-20) alkylamidoalkyl, C (1-20) amidoalkyl, C (1-20) acetamidoalkyl, C (1-20) alkenyl, C (1-20) alkynyl, C (3-8) alkoxyl, C (1-11) alkoxyalkyl, and C (1-20) dialkoxyalkyl.
    发现将六元环结构融合到五元环结构的新型杂环化合物对治疗和预防与受白细胞介素-12(“IL-12”)胞内信号传导受影响的疾病相关的症状或表现是有用的,例如Th1细胞介导的疾病。这些治疗化合物、药学上可接受的衍生物(例如,其解旋异构体、二对映异构体、互变异构体、盐和溶剂)或其前药具有以下一般公式:每个X、Y和Z独立地选择自C(R3)、N、N(R3)和S的群体之一。每个R1、R2和R3被取代或未取代,并且独立地选择自氢、卤、氧、C(1-20)烷基、C(1-20)羟基烷基、C(1-20)硫烷基、C(1-20)烷基胺、C(1-20)烷基胺烷基、C(1-20)胺基烷基、C(1-20)胺基甲氧基烯基、C(1-20)胺基甲氧基炔基、C(1-20)二胺基烷基、C(1-20)三胺基烷基、C(1-20)四胺基烷基、C(5-15)氨基三烷氧基氨基、C(1-20)烷基酰胺、C(1-20)烷基酰胺烷基、C(1-20)酰胺基烷基、C(1-20)乙酰胺基烷基、C(1-20)烯基、C(1-20)炔基、C(3-8)烷氧基、C(1-11)烷氧基烷基和C(1-20)二烷氧基烷基。
  • Xanthine modulators of metabolism of cellular P-450
    申请人:Cell Therapeutics, Inc.
    公开号:US06075029A1
    公开(公告)日:2000-06-13
    A new class of xanthine compounds, variously substituted at the 1, 3, 7 and 8 positions, is characterized by an ability to modulate the activity of key enzymes involved in drug metabolism. These compounds generally are useful in affecting drug metabolism and, particularly, in extending the circulating half-life of compounds that are metabolized via P-450-mediated pathways.
    一类新的黄嘌呤化合物,在1、3、7和8位置各异取代,具有调节参与药物代谢的关键酶活性的能力。这些化合物通常对影响药物代谢有用,特别是在延长通过P-450介导途径代谢的化合物的循环半衰期方面。
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(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物