39716-58-0
4-pentenoyl chloride
CAS: 39716-58-0
Molecular Formula: C5H7ClO
39716-58-0 - Names and Identifiers
| Name | 4-pentenoyl chloride |
| Synonyms | 4-pentenoyl chloride pent-4-enoyl chloride 4-Pentenoic acid chloride 33249 4-pentenoyl chloride |
| CAS | 39716-58-0 |
| InChI | InChI=1/C5H7ClO/c1-2-3-4-5(6)7/h2H,1,3-4H2 |
| InChIKey | JDKQTIKEGOOXTJ-UHFFFAOYSA-N |
39716-58-0 - Physico-chemical Properties
| Molecular Formula | C5H7ClO |
| Molar Mass | 118.56 |
| Density | 1.033g/cm3 |
| Boling Point | 125.1°C at 760 mmHg |
| Flash Point | 35.9°C |
| Vapor Presure | 12.4mmHg at 25°C |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.433 |
39716-58-0 - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R10 - Flammable R34 - Causes burns |
| Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. 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 whenever possible.) |
| UN IDs | UN 2920 |
| WGK Germany | 3 |
39716-58-0 - Upstream Downstream Industry
| Downstream Products | 4-PENTENAL 5-AMINOMETHYL-PYRROLIDIN-2-ONE |
39716-58-0 - Introduction
4-pentenoyl chloride(4-pentenoyl chloride) is an organic compound having the form of a colorless liquid. Its chemical formula is C5H7ClO, and in the molecule, the pentenoic acid group is attached to the chlorine atom. It has a pungent odor and is soluble in organic solvents.
4-pentenoyl chloride has certain application value in organic synthesis. It can be used as a starting material for the synthesis of other organic compounds, such as esters, ethers and amides. In addition, it can also be used to prepare other organic compounds, such as anhydrides and fatty acid derivatives.
The preparation of 4-pentenoyl chloride can be completed by reacting pentenoic acid with thionyl chloride. The specific preparation method is as follows: First, pentenoic acid is reacted with thionyl chloride under appropriate temperature and conditions to produce 4-pentenoyl sulfoxide. The 4-pentenoyl sulfoxide is then converted to the 4-pentenoyl chloride by reaction with hydrogen chloride.
Regarding its safety information, 4-pentenoyl chloride is an irritating compound and should avoid skin contact and inhalation. Appropriate handling measures, such as gloves, goggles and protective clothing, are required during use. When stored, it should be kept in a sealed container and away from fire and oxidizing agents.
4-pentenoyl chloride has certain application value in organic synthesis. It can be used as a starting material for the synthesis of other organic compounds, such as esters, ethers and amides. In addition, it can also be used to prepare other organic compounds, such as anhydrides and fatty acid derivatives.
The preparation of 4-pentenoyl chloride can be completed by reacting pentenoic acid with thionyl chloride. The specific preparation method is as follows: First, pentenoic acid is reacted with thionyl chloride under appropriate temperature and conditions to produce 4-pentenoyl sulfoxide. The 4-pentenoyl sulfoxide is then converted to the 4-pentenoyl chloride by reaction with hydrogen chloride.
Regarding its safety information, 4-pentenoyl chloride is an irritating compound and should avoid skin contact and inhalation. Appropriate handling measures, such as gloves, goggles and protective clothing, are required during use. When stored, it should be kept in a sealed container and away from fire and oxidizing agents.
Last Update：2024-04-10 22:29:15
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View History
39716-58-0
3121-77-5
1546532-98-2
改良剂
1095005-59-6
116-17-6
13815-94-6
593-33-9
95668-20-5
2-(3-(prop-1-en-2-yl)phenyl)-1,3-dioxolane
3121-77-5
1546532-98-2
改良剂
1095005-59-6
116-17-6
13815-94-6
593-33-9
95668-20-5
2-(3-(prop-1-en-2-yl)phenyl)-1,3-dioxolane
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