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6-苯氧基己基溴 | 51795-97-2

中文名称
6-苯氧基己基溴
中文别名
6-溴己基苯醚
英文名称
6-bromohexyloxybenzene
英文别名
6-phenoxyhexyl bromide;1-(6-bromohexyloxy) benzene;6-bromo-1-phenoxy hexane;6-bromohexoxybenzene
6-苯氧基己基溴化学式
CAS
51795-97-2
化学式
C12H17BrO
mdl
——
分子量
257.17
InChiKey
QOLSAZPSEJXYSH-UHFFFAOYSA-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:
    172-174 °C(Press: 13 Torr)
  • 密度:
    1.229±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    14
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2909309090
  • 储存条件:
    室温

SDS

SDS:a5e7f0a5c5bb6b1aaabf9a0331e26944
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6-Phenoxyhexyl Bromide
SAFETY DATA SHEET

Section 1. IDENTIFICATION
Product name: 6-Phenoxyhexyl Bromide

Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS Not classified
Not classified
HEALTH HAZARDS
ENVIRONMENTAL HAZARDS Not classified
GHS label elements, including precautionary statements
Pictograms or hazard symbols None
No signal word
Signal word
Hazard statements None
None
Precautionary statements:

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: 6-Phenoxyhexyl Bromide
Percent: >95.0%(GC)
CAS Number: 51795-97-2
Synonyms: 6-Bromohexyl Phenyl Ether
Chemical Formula: C12H17BrO

Section 4. FIRST AID MEASURES
Inhalation: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Get medical advice/attention if you feel unwell.
Skin contact: Remove/Take off immediately all contaminated clothing. Rinse skin with
water/shower. If skin irritation or rash occurs: Get medical advice/attention.
Eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Ingestion: Get medical advice/attention if you feel unwell. Rinse mouth.
Protection of first-aiders: A rescuer should wear personal protective equipment, such as rubber gloves and air-
tight goggles.

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, water spray, carbon dioxide.
media:
Unsuitable extinguishing Solid streams of water
media:
Specific hazards arising Take care as it may decompose upon combustion or in high temperatures to
from the chemical: generate poisonous fume.
6-Phenoxyhexyl Bromide

Section 5. FIRE-FIGHTING MEASURES
Precautions for firefighters: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

Section 6. ACCIDENTAL RELEASE MEASURES
Use personal protective equipment. Keep people away from and upwind of spill/leak.
Personal precautions,
protective equipment and Ensure adequate ventilation. Entry to non-involved personnel should be controlled
emergency procedures: around the leakage area by roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Absorb spilled material in a suitable absorbent (e.g. rag, dry sand, earth, saw-dust).
containment and cleaning In case of large amount of spillage, contain a spill by bunding. Adhered or collected
up: material should be promptly disposed of, in accordance with appropriate laws and
regulations.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent generation of vapour or mist. Wash hands and face thoroughly after
handling.
Use a ventilation, local exhaust if vapour or aerosol will be generated.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Conditions for safe storage, including any
incompatibilities
Storage conditions: Keep container tightly closed. Store in a cool and dark place.
Store away from incompatible materials such as oxidizing agents.
Packaging material: Comply with laws.

Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Install a closed system or local exhaust as possible so that workers should not be
Engineering controls:
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Vapor respirator. Follow local and national regulations.
Hand protection: Protective gloves.
Eye protection: Safety glasses. A face-shield, if the situation requires.
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Liquid
Form: Clear
Very pale yellow - Pale yellow
Colour:
Odour: No data available
pH: No data available
Melting point/freezing point:No data available
112°C/0.03kPa
Boiling point/range:
Flash point: No data available
Flammability or explosive
limits:
No data available
Lower:
Upper: No data available
1.25
Relative density:
Solubility(ies):
No data available
[Water]
[Other solvents] No data available
6-Phenoxyhexyl Bromide

Section 10. STABILITY AND REACTIVITY
Chemical stability: Stable under proper conditions.
Possibility of hazardous No special reactivity has been reported.
reactions:
Incompatible materials: Oxidizing agents
Hazardous decomposition Carbon monoxide, Carbon dioxide, Hydrogen bromide
products:

Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: No data available
Skin corrosion/irritation: No data available
Serious eye No data available
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
IARC = No data available
No data available
NTP =
Reproductive toxicity: No data available

Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
Crustacea: No data available
Algae: No data available
Persistence / degradability: No data available
Bioaccumulative No data available
potential(BCF):
Mobility in soil
No data available
Log Pow:
Soil adsorption (Koc): No data available
Henry's Law No data available
constant(PaM3/mol):

Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to burn in a chemical
incinerator equipped with an afterburner and scrubber system. Observe all federal, state and local regulations when
disposing of the substance.

Section 14. TRANSPORT INFORMATION
Does not correspond to the classification standard of the United Nations
Hazards Class:
UN-No: Not listed

Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26, 2002
and revised on February 16,2011): Safe use and production, the storage of a dangerous chemical, transport,
loading and unloading were prescribed.
6-Phenoxyhexyl Bromide


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2
    • 3

反应信息

  • 作为反应物:
    描述:
    6-苯氧基己基溴 在 sodium iodide 作用下, 以 丙酮 为溶剂, 反应 6.0h, 生成 ((6-iodohexyl)oxy)benzene
    参考文献:
    名称:
    用于合成脂肪族酯的烷基碘的铜催化烷氧基羰基化反应:氢气有所不同
    摘要:
    已开发出铜催化的未活化烷基碘的烷氧基羰基化转化。各种烷基碘可以以良好的产率转化为相应的叔丁基酯。NaO t Bu 既是亲核试剂又是碱。此外,如果添加额外的醇,也可以中等收率获得其他类型的脂肪族酯。伯醇和仲烷基醇均可成功反应。
    DOI:
    10.1021/acs.orglett.1c03071
  • 作为产物:
    描述:
    6-溴正己醇四溴化碳potassium carbonate三苯基膦 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 生成 6-苯氧基己基溴
    参考文献:
    名称:
    人组蛋白脱乙酰基酶的新型抑制剂:基于SAHA的非异羟肟酸酯的设计,合成,酶抑制和癌细胞生长抑制。
    摘要:
    为了找到新型的非异羟肟酸酯组蛋白脱乙酰基酶(HDAC)抑制剂,设计并合成了以亚磺酰苯胺异羟肟酸(SAHA)为模型的一系列化合物。在该系列中,发现化合物7(其中SAHA的异羟肟酸被硫醇替代)与SAHA一样有效,该系列的优化导致鉴定出比SAHA更有效的HDAC抑制剂。在癌细胞生长抑制测定中,S-异丁酰基衍生物51显示出强活性,并且其效力与SAHA相当。通过Western印迹分析证实癌细胞生长抑制活性是组蛋白过度乙酰化和随后诱导p21(WAF1 / CIP1)的结果。
    DOI:
    10.1021/jm049207j
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文献信息

  • Sensitivity booster for mass detection enables unambiguous analysis of peptides, proteins, antibodies, and protein bioconjugates
    作者:Rohith Singudas、Neelesh C. Reddy、Vishal Rai
    DOI:10.1039/c9cc03424b
    日期:——

    A chemical tag enhances peptide detection by multiple orders in mass spectrometry.

    一种化学标记可使肽段在质谱中的检测增强数个数量级。
  • [EN] CHEMOSELECTIVE SENSITIVITY BOOSTER FOR TAGGING A PEPTIDE, PEPTIDE CONJUGATE, OR SIMILAR REACTIVE MOLECULE<br/>[FR] AMPLIFICATEUR DE SENSIBILITÉ CHIMIOSÉLECTIF POUR MARQUER UN PEPTIDE, UN CONJUGUÉ PEPTIDIQUE OU UNE MOLÉCULE RÉACTIVE SIMILAIRE
    申请人:INDIAN INSTITUTE OF SCIENCE EDUCATION AND RES BHOPAL
    公开号:WO2020245843A1
    公开(公告)日:2020-12-10
    The invention pertains to chemoselective sensitivity booster for tagging a peptide, peptide conjugate, or similar reactive molecule for analysis of a peptide, protein, antibody, protein bioconjugate, antibody bioconjugate, and similar analytes. The sensitivity booster comprises of sp2 or sp3 nitrogen centers in combination with hydrophobic carbon chains linked with an electrophile or nucleophile for attachment with a peptide, peptide conjugate, or molecules with similar reactivity.
    这项发明涉及一种化学选择性增敏剂,用于标记肽、肽共轭物或类似的反应分子,以便分析肽、蛋白质、抗体、蛋白生物共轭物、抗体生物共轭物和类似的分析物。该增敏剂包括与亲水碳链结合的sp2或sp3氮中心,与带有亲电子或亲核子的肽、肽共轭物或具有类似反应性的分子结合。
  • Modifications of primaquine as antimalarials. 4. 5-Alkoxy derivatives of primaquine
    作者:Eugene H. Chen、Keiichi Tanabe、Andrew J. Saggiomo、Edward A. Nodiff
    DOI:10.1021/jm00390a012
    日期:1987.7
    blood schizonticides (Plasmodium berghei, mouse) and tissue schizonticides (Plasmodium cynomolgi, monkey). Several of these compounds were extremely active in both screens. Such a broad spectrum of antimalarial efficacy offers the possibility of a single drug that could cure the various relapsing and nonrelapsing malarias.
    已经合成了三十二个5-烷氧基伯氨喹,并被评估为血型裂殖剂(伯氏疟原虫,小鼠)和组织型裂殖剂(食蟹毛疟原虫,猴子)。这些化合物中的几种在两种筛选中均具有极高的活性。如此广泛的抗疟疾功效提供了一种可以治愈各种复发性和非复发性疟疾的药物。
  • An Efficient Oxidation of Primary Azides Catalyzed by Copper Iodide: A Convenient Method for the Synthesis of Nitriles
    作者:Manjunath Lamani、Kandikere Ramaiah Prabhu
    DOI:10.1002/anie.201002635
    日期:2010.9.3
    A wide range of primary azides have been efficiently oxidized by a catalytic amount of CuI and TBHP into their corresponding nitriles in aqueous solution. A variety of oxidizable functional groups were well tolerated under the reaction conditions, and oxidation of secondary azides furnished their corresponding ketones (see scheme; TBHP=tert‐butyl hydroperoxide).
    多种伯叠氮化物已通过催化量的CuI和TBHP在水溶液中被有效氧化为相应的腈。在反应条件下,各种可氧化的官能团均具有良好的耐受性,仲叠氮化物的氧化作用提供了它们相应的酮(参见方案; TBHP =叔丁基氢过氧化物)。
  • An efficient transformation of primary halides into nitriles through palladium-catalyzed hydrogen transfer reaction
    作者:Tao Zou、Xiaoqiang Yu、Xiujuan Feng、Ming Bao
    DOI:10.1039/c5cc03429a
    日期:——
    Two-step one-pot transformation of primary halides into corresponding nitriles is successfully achieved. Nucleophilic substitution of primary halides with sodium azide and subsequent palladium-catalyzed hydrogen transfer proceed smoothly in the presence...
    成功实现了初级卤化物到相应腈的两步一锅转化。在存在条件下,用叠氮化钠亲核取代卤代伯卤化物并随后进行钯催化的氢转移...
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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