Cinnamoyl chloride

CAS No.:*******1 

Molecular Formula:C9H7ClO

Molecular Weight:**6.**4 g/mol

Synonym:Cinnamoyl chloride;*-Phenyl**-propenoyl chloride;*-Phenylpropenoyl chloride;

EINECS No.:********5

FEMA No.:***7

Density:1.***7 g/cm3 (*0 C)

Melting point:****7 °C(lit.)

Boiling point:******8 °C(lit.)

Purity:≥*8%

Appearance: white or yellowish crystal

Storage temp:**6°C

Partition Coefficient：3.*9

Heat Of Vaporization：*9.5 kJ/mol

Water-solubility:Soluble in petroleum ether, carbon tetrachloride and hot ethanol, insoluble in water. Slowly decompose in water. 

Storage

Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Refrigerator (approx 4 C). Store protected from moisture.

Handling

Keep container tightly closed. Do not get on skin or in eyes. Do not ingest or inhale. Use with adequate ventilation. Discard contaminated shoes.

 

Application:

Used as an intermediate in organic synthesis for the determination of trace moisture. 

This product can be used as an intermediate in organic synthesis. Cinnamamide can be prepared by amidation, and n-cinnamyl -nphenylhydroxylamine can be prepared by interaction with phenylhydroxylamine. Cinnamyl chloride can also be used to synthesize the anti-inflammatory and analgesic drug Sinnoxicam (cinnoxicam) and other fine chemicals. A reagent for the determination of trace water.

 

 

Production preparation:

Cinnamyl chloride is obtained by the reaction of sodium cinnamate with acetyl chloride. The acetyl chloride and benzene are mixed into solution, and the dried sodium cinnamate is added several times under stirring from time to time. After each addition, the carbon dioxide is released and the next time is added. Then reflux for 2 hours. After a little cooling, the resulting sodium chloride and trace unreacted sodium cinnamate are filtered out. The filtrate was distilled to remove benzene at atmospheric pressure and then distilled at **1C (1.*7kPa) to obtain the product in ****0 yield. Carbon tetrachloride can be recrystallized when purification is needed. Cinnamyl chloride was prepared by the reaction of cinnamic acid with dichloro sulfoxide.

 

Polyvinyl cinnamate adhesive (PVAC,) is a linear polymer compound with molecular weight of ****0 ~ *0 **0, which is obtained by esterification of polyvinyl alcohol and cinnamyl chloride. The photosensitive adhesive was prepared by adding *-nitroacenaphthene and organic solvent cyclohexanone, that is, the double bond of the molecule was opened and solidified under ultraviolet light irradiation. It has important applications in the manufacture of integrated circuits and micro components. A photoresist, polyvinyl cinnamate, synthesized from polyvinyl alcohol and cinnamyl chloride in a pyridine solvent. The prepared photoresist is called KPR.. The photochemical dimerization of the double bond of cinnamate was formed under the action of ultraviolet light, and it was turned into an insoluble substance. KPR was the first photoresist used in photolithography, and *-nitroacenaphthene was usually added as Guang Min. Photoresist, also known as photoresist, can be used in photolithography, which is widely used in printing and electronic industry. Its working principle is that the light part is crosslinked to form the insoluble hardening film, which is processed into negative image (negative glue), or the original insoluble glue becomes soluble after illumination, and is processed as a positive image (positive glue).