Cinnamyl chloride
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Cinnamyl chloride
structure -
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CAS No:
2687-12-9
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Formula:
C9H9Cl
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Chemical Name:
Cinnamyl chloride
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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:
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CAS No:
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
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.
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
Recommended Suppliers of Cinnamyl chloride
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