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Cinnamyl chloride

Cinnamyl chloride structure

Cinnamyl chloride 

structure
  • CAS No:

    2687-12-9

  • Formula:

    C9H9Cl

  • Chemical Name:

    Cinnamyl chloride

  • Synonyms:

    Benzene,(3-chloro-1-propen-1-yl)-;Benzene,(3-chloropropenyl)-;Benzene,(3-chloro-1-propenyl)-;Benzene,(γ-chloropropenyl)-;(3-Chloro-1-propen-1-yl)benzene;Cinnamyl chloride;1-Propene,3-chloro-1-phenyl-;1-Chloro-3-phenyl-2-propene;3-Chloro-1-phenylpropene;3-Phenyl-2-propenyl chloride;β-Chloromethylstyrene;3-Phenyl-2-propen-1-yl chloride;(3-Chloro-1-propenyl)benzene;3-Chloro-1-phenyl-1-propene;3-Phenylallyl chloride;NSC 5599;3-Chloroprop-1-en-1-ylbenzene

  • Categories:

    Flavors and Fragrances  >  Synthetic Fragrances

Description

yellow to yellow-brown liquid

Cinnamyl chloride Basic Attributes

152.62

152.62

741974

220-246-4

2I1ADL56TX

5599

DTXSID70175315

2942000000

Characteristics

0

3.2

Yellow to yellow-brown Liquid

1.1±0.1 g/cm3

35 °C

121-122 °C @ Press: 14 Torr

175 °F

1.577

H2O: 0.2 g/L (20 ºC)

Refrigerator (+4°C)

Safety Information

III

8

UN 1760 8/PG 2

3

22-26-34-43-36

26-28-36/37/39-45-28A-23-27

CZ0919905

T+,C

Corrosive/Lachrymatory

P260, P261, P264, P270, P271, P272, P280, P284, P285, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P320, P321, P330, P333+P313, P342+P311, P363, P403+P233, P405, P501

H302

|Danger|H302 (79.25%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P261, P264, P270, P271, P272, P280, P284, P285, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P320, P321, P330, P333+P313, P342+P311, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 53 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H227 (100%): Combustible liquid [Warning Flammable liquids]|P210, P260, P261, P264, P270, P271, P280, P284, P285, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P320, P321, P330, P342+P311, P363, P370+P378, P403+P233, P403+P235, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Cinnamyl chloride Use and Manufacturing

Methods of Manufacturing

Derived from styrene by chloromethylation. Add hydrochloric acid and formaldehyde into the reaction pot, add styrene with stirring, and heat to reflux for 3h. Let it stand for 1 hour to separate the waste acid from the lower layer, and add anhydrous calcium chloride to the upper reaction solution to obtain cinnamyl chloride.

Uses

Organic chemical industry, drug synthesis

Benzene, (3-chloro-1-propen-1-yl)-: ACTIVE

Computed Properties

Molecular Weight:152.62
XLogP3:3.2
Rotatable Bond Count:2
Exact Mass:152.0392780
Monoisotopic Mass:152.0392780
Heavy Atom Count:10
Complexity:101
Defined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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