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2,4-戊二烯酸 | 21651-12-7

中文名称
2,4-戊二烯酸
中文别名
反式-2,4-戊二烯酸;(E)-2,4-戊二烯酸
英文名称
(E)-2,4-pentadienoic acid
英文别名
(E)-penta-2,4-dienoic acid;trans-2,4-pentadienoic acid;2,4-pentadienoic acid;pentadienoic acid;(2E)-penta-2,4-dienoic acid;Penta-2,4-dienoic acid
2,4-戊二烯酸化学式
CAS
21651-12-7
化学式
C5H6O2
mdl
——
分子量
98.1014
InChiKey
SDVVLIIVFBKBMG-ONEGZZNKSA-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

  • 熔点:
    72℃
  • 沸点:
    215℃
  • 密度:
    1.039
  • 闪点:
    121℃
  • 溶解度:
    可溶于氯仿(少许)、甲醇(少许)
  • 保留指数:
    922.2

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    8
  • 海关编码:
    2916190090
  • 包装等级:
    III
  • 危险类别:
    8
  • 危险品运输编号:
    UN 1759
  • 危险性防范说明:
    P280,P301+P310,P305+P351+P338,P310
  • 危险性描述:
    H301,H314
  • 储存条件:
    -20°C,避光保存,需使用惰性气体保护。

SDS

SDS:137c7a7d5723099b23f29462d80b3f68
查看

Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product identifiers
Product name : trans-2,4-Pentadienoic acid
CAS-No. : 21651-12-7
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008 [EU-GHS/CLP]
Acute toxicity, Oral (Category 3)
Skin corrosion (Category 1B)
Skin sensitization (Category 1)
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Toxic if swallowed. Causes burns. May cause sensitization by skin contact.
Label elements
Labelling according Regulation (EC) No 1272/2008 [CLP]
Pictogram
Signal word Danger
Hazard statement(s)
H301 Toxic if swallowed.
H314 Causes severe skin burns and eye damage.
H317 May cause an allergic skin reaction.
Precautionary statement(s)
P280 Wear protective gloves/ protective clothing/ eye protection/ face
protection.
P301 + P310 IF SWALLOWED: Immediately call a POISON CENTER or doctor/
physician.
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact lenses, if present and easy to do. Continue rinsing.
P310 Immediately call a POISON CENTER or doctor/ physician.
Supplemental Hazard none
Statements
According to European Directive 67/548/EEC as amended.
Hazard symbol(s)
R-phrase(s)
R25 Toxic if swallowed.
R34 Causes burns.
R43 May cause sensitization by skin contact.
S-phrase(s)
S26 In case of contact with eyes, rinse immediately with plenty of water and
seek medical advice.
S36/37/39 Wear suitable protective clothing, gloves and eye/face protection.
S45 In case of accident or if you feel unwell, seek medical advice immediately
(show the label where possible).
Other hazards - none

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substances
Formula : C5H6O2
Molecular Weight : 98,1 g/mol
Component Concentration
trans-2,4-Pentadienoic acid
CAS-No. 21651-12-7 -

Section 4. FIRST AID MEASURES
Description of 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
Take off contaminated clothing and shoes immediately. Wash off with soap and plenty of water. Take
victim immediately to hospital. 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
Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Rinse mouth with
water. Consult a physician.
Most important symptoms and effects, both acute and delayed
Material is extremely destructive to tissue of the mucous membranes and upper respiratory tract, eyes, and
skin., spasm, inflammation and edema of the larynx, spasm, inflammation and edema of the bronchi,
pneumonitis, pulmonary edema, burning sensation, Cough, wheezing, laryngitis, Shortness of breath,
Headache, Nausea
Indication of any immediate medical attention and special treatment needed
no data available

Section 5. FIREFIGHTING MEASURES
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides
Advice for firefighters
Wear self contained breathing apparatus for fire fighting if necessary.
Further information
no data available

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, protective equipment and emergency procedures
Wear respiratory protection. 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. Discharge into the
environment must be avoided.
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.
Reference to other sections
For disposal see section 13.

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, including any incompatibilities
Store in cool place. 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.
Specific end use(s)
no data available

Section 8. EXPOSURE CONTROLS/PERSONAL PROTECTION
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Avoid contact with skin, eyes and clothing. Wash hands before breaks and immediately after handling
the product.
Personal protective equipment
Eye/face protection
Tightly fitting safety goggles. Faceshield (8-inch minimum). Use equipment for eye protection
tested and approved under appropriate government standards such as NIOSH (US) or EN
166(EU).
Skin 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.
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.
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).

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Information on basic physical and chemical properties
a) Appearance Form: liquid
b) Odour no data available
c) Odour Threshold no data available
d) pH no data available
e) Melting point/freezing Melting point/range: 71 - 76 °C
point
f) Initial boiling point and no data available
boiling range
g) Flash point no data available
h) Evaporation rate no data available
i) Flammability (solid, gas) no data available
j) Upper/lower no data available
flammability or
explosive limits
k) Vapour pressure no data available
l) Vapour density no data available
m) Relative density no data available
n) Water solubility no data available
o) Partition coefficient: n- log Pow: 1,207
octanol/water
p) Auto-ignition no data available
temperature
q) Decomposition no data available
temperature
r) Viscosity no data available
s) Explosive properties no data available
t) Oxidizing properties no data available
Other safety information
no data available

Section 10. STABILITY AND REACTIVITY
Reactivity
no data available
Chemical stability
no data available
Possibility of hazardous reactions
no data available
Conditions to avoid
no data available
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
Other decomposition products - no data available

Section 11. TOXICOLOGICAL INFORMATION
Information on toxicological effects
Acute toxicity
no data available
Skin corrosion/irritation
no data available
Serious eye damage/eye irritation
no data available
Respiratory or skin sensitization
May cause allergic skin reaction.
Germ cell mutagenicity
no data available
Carcinogenicity
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
no data available
Specific target organ toxicity - repeated exposure
no data available
Aspiration hazard
no data available
Potential health effects
Inhalation
May be harmful if inhaled. Material is extremely destructive to the tissue of
the mucous membranes and upper respiratory tract.
Ingestion Toxic if swallowed. Causes burns.
Skin May be harmful if absorbed through skin. Causes skin burns.
Eyes
Causes eye burns.
Signs and Symptoms of Exposure
Material is extremely destructive to tissue of the mucous membranes and upper respiratory tract, eyes, and
skin., spasm, inflammation and edema of the larynx, spasm, inflammation and edema of the bronchi,
pneumonitis, pulmonary edema, burning sensation, Cough, wheezing, laryngitis, Shortness of breath,
Headache, Nausea
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
Results of PBT and vPvB assessment
no data available
Other adverse effects
Toxic to aquatic life.
no data available

Section 13. DISPOSAL CONSIDERATIONS
Waste treatment methods
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
UN number
ADR/RID: 3261 IMDG: 3261 IATA: 3261
UN proper shipping name
ADR/RID: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S. (trans-2,4-Pentadienoic acid)
IMDG: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S. (trans-2,4-Pentadienoic acid)
IATA: Corrosive solid, acidic, organic, n.o.s. (trans-2,4-Pentadienoic acid)
Transport hazard class(es)
ADR/RID: 8 IMDG: 8 IATA: 8
Packaging group
ADR/RID: II IMDG: II IATA: II
Environmental hazards
ADR/RID: no IMDG Marine Pollutant: no IATA: no
Special precautions for user
no data available



SECTION 15 - REGULATORY INFORMATION
N/A


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

反应信息

  • 作为反应物:
    描述:
    2,4-戊二烯酸吡啶 、 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 焦磷酸硫胺素1-羟基苯并三唑溶剂黄146N,N-二异丙基乙胺三氟乙酸[双(三氟乙酰氧基)碘]苯 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 生成 N-[(6-amino-2-methylpyridin-3-yl)methyl]-2-[3-(4-chlorophenyl)sulfanyl-1-oxo-1-pyrrolidin-1-ylpropan-2-yl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-a]pyridazine-5-carboxamide
    参考文献:
    名称:
    高通量合成和凝血酶抑制剂的优化通过尿素α-添加和迈克尔添加。
    摘要:
    已经开发了一种新的丙酸酯向尿嘧啶的α加成法,然后迈克尔加成各种亲核试剂,以快速生产和优化拟肽药物前导。该技术已经产生了许多高度有效和选择性的丝氨酸蛋白酶凝血酶抑制剂。
    DOI:
    10.1016/s0960-894x(03)00155-0
  • 作为产物:
    参考文献:
    名称:
    Chiusoli, Gazzetta Chimica Italiana, 1959, vol. 89, p. 1343,1346
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • FIBROSIS INHIBITOR
    申请人:Sumitomo Pharmaceuticals Company, Limited
    公开号:EP1479384A1
    公开(公告)日:2004-11-24
    Medicament being useful as a fibrosis inhibitor for organs or tissues, which comprises a compound of the formula (I): wherein Ring Z is optionally substituted pyrrole ring, etc.; W2 is -CO-, -SO2-, optionally substituted C1-C4 alkylene, etc.; Ar2 is optionally substituted aryl, etc.; W1 and Ar1 mean the following (1) and (2): (1) W1 is optionally substituted C1-C4 alkylene, etc.; Ar1 is optionally substituted bicyclic heteroaryl having 1 to 4 nitrogen atoms as ring-forming atoms: (2) W1 is optionally substituted C2-C5 alkylene, optionally substituted C2-C5 alkenylene, etc.; and Ar1 is aryl or monocyclic heteroaryl, which is substituted by carboxyl, alkoxycarbonyl, etc. at the ortho- or meta-position thereof with respect to the binding position of W1, or a pharmaceutically acceptable salt thereof.
    药物作为器官或组织的纤维化抑制剂而有用,包括具有以下式(I)的化合物: 其中环Z是可选择取代的吡咯环等;W2是-CO-,-SO2-,可选择取代的C1-C4烷基等;Ar2是可选择取代的芳基等;W1和Ar1表示如下(1)和(2): (1)W1是可选择取代的C1-C4烷基等;Ar1是可选择取代的具有1至4个氮原子作为环形成原子的双环杂芳基: (2)W1是可选择取代的C2-C5烷基,可选择取代的C2-C5烯基等;以及 Ar1是芳基或单环杂芳基,其在相对于W1的结合位置的邻位或间位处被羧基,烷氧羰基等取代, 或其药学上可接受的盐。
  • Reaction Discovery by Using a Sandwich Immunoassay
    作者:Julia Quinton、Sergii Kolodych、Manon Chaumonet、Valentina Bevilacqua、Marie-Claire Nevers、Hervé Volland、Sandra Gabillet、Pierre Thuéry、Christophe Créminon、Frédéric Taran
    DOI:10.1002/anie.201201451
    日期:2012.6.18
    Mmm, a reaction sandwich…︁ Using an immunoassay‐based technique able to monitor any kind of cross‐coupling reaction, a systematic and rapid evaluation of a large panel of random reactions was carried out. This approach led to the discovery of two new copper‐promoted reactions: a desulfurization reaction of thioureas leading to isoureas and a cyclization reaction leading to thiazole derivatives from
    嗯,反应夹心……︁使用基于免疫分析的技术能够监测任何种类的交叉偶联反应,对大量随机反应进行了系统,快速的评估。这种方法导致发现了两个新的铜促进的反应:硫脲的脱硫反应导致异脲,环化反应导致炔烃和N-羟基硫脲的噻唑衍生物。
  • Non-Amide-Based Combinatorial Libraries Derived fromN-Boc-Iminodiacetic Acid: Solution-Phase Synthesis of Piperazinone Libraries with Activity Against LEF-1/β-Catenin-Mediated Transcription
    作者:Dale L. Boger、Joel Goldberg、Shigeki Satoh、Yves Ambroise、Steven B. Cohen、Peter K. Vogt
    DOI:10.1002/1522-2675(20000809)83:8<1825::aid-hlca1825>3.0.co;2-4
    日期:2000.8.9
    methodology was applied to the synthesis of a diverse 150-member library with substituents in three positions of the piperazinone core. Screening results from a luciferase reporter assay indicate that a number of library members are novel repressors of LEF-1/β-catenin-mediated transcription, and may be effective agents against colorectal tumors. Two secondary libraries (100 members each) designed from
    详细介绍了从 N-Boc-亚氨基二乙酸开始仅需四个步骤即可快速、平行合成高度官能化哌嗪酮的溶液相方法。这些努力代表了组合文库的溶液相合成从 N-Boc-亚氨基二乙酸扩展到基于非酰胺的文库,其中使用简单的液-液萃取来纯化所有反应产物。该方法被应用于合成一个多样化的 150 成员库,在哌嗪酮核心的三个位置具有取代基。荧光素酶报告基因检测的筛选结果表明,许多文库成员是 LEF-1/β-连环蛋白介导的转录的新阻遏物,可能是对抗结肠直肠肿瘤的有效药物。合成和筛选了从这些先导结构设计的两个二级库(每个 100 个成员),提供额外的活性剂并深入了解该系列中的关键结构-活性关系。这些化合物仅代表第二类小分子,其抑制含有 LEF-1 响应元件的报告基因的转录,第一类不基于 DNA 小沟结合剂。
  • Developing piperine towards TRPV1 and GABA<sub>A</sub> receptor ligands – synthesis of piperine analogs via Heck-coupling of conjugated dienes
    作者:Laurin Wimmer、David Schönbauer、Peter Pakfeifer、Angela Schöffmann、Sophia Khom、Steffen Hering、Marko D. Mihovilovic
    DOI:10.1039/c4ob02242d
    日期:——
    pungent alkaloid of black pepper, and several of its derivatives are modulators of gamma-amino butyric acid type A (GABAA) receptors. Concomitantly, this natural product has also been reported to activate transient receptor potential vanilloid type 1 (TRPV1) receptors. We have developed a Heck cross-coupling reaction of conjugated dienamides enabling the rapid assembly of piperine derivatives containing
    黑胡椒的刺激性生物碱胡椒碱及其几种衍生物是 γ-氨基丁酸 A 型 (GABAA) 受体的调节剂。同时,据报道,这种天然产物还可以激活瞬时受体电位香草素 1 型 (TRPV1) 受体。我们开发了共轭二酰胺的 Heck 交叉偶联反应,能够快速组装含有改性芳香核心的胡椒碱衍生物。在评估重点化合物库后,确定了关键的芳香族取代基,选择性地影响 GABAA 或 TRPV1 受体。
  • The reaction of fluorine-containing compounds with conjugated dienoic acids initiated by sodium dithionite
    作者:Shengjie Mao、Xiang Fang、Lu Ba、Fanhong Wu
    DOI:10.1016/j.jfluchem.2006.09.004
    日期:2007.1
    The reaction of fluorine-containing halides and acetamides with conjugated dienoic acids initiated by sodium dithionite gave halide-free 1,4-adducts in 40–80% yields, with the E configuration as the major products.
    连二亚硫酸钠引发的含氟卤化物和乙酰胺与共轭二烯酸的反应以40-80%的收率得到了无卤的1,4-加合物,其中E构型为主要产物。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
cnmr
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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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