C81101
Cinnamoyl chloride
≥95.0%
Synonym(s):
trans-3-Phenylacryloyl chloride
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About This Item
Linear Formula:
C6H5CH=CHCOCl
CAS Number:
Molecular Weight:
166.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-065-5
Beilstein/REAXYS Number:
606265
MDL number:
Assay:
≥95.0%
Form:
solid
InChI
1S/C9H7ClO/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H/b7-6+
InChI key
WOGITNXCNOTRLK-VOTSOKGWSA-N
SMILES string
ClC(=O)\C=C\c1ccccc1
assay
≥95.0%
form
solid
bp
256-258 °C (lit.)
mp
35-37 °C (lit.)
storage temp.
2-8°C
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signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Bianca Pérez et al.
Bioorganic & medicinal chemistry letters, 23(3), 610-613 (2013-01-08)
Novel 9-aminoacridine derivatives were synthesized by linking the heteroaromatic core to different cinnamic acids through an aminobutyl chain. The test compounds demonstrated mid-nanomolar in vitro activity against erythrocytic stages of the chloroquine-resistant W2 strain of the human malaria parasite Plasmodium
Shinya Yano et al.
Carbohydrate polymers, 184, 418-426 (2018-01-22)
Biocompatibility of cinnamoyl-modified carbohydrate materials is not well-known, while they are attracting attention as a photoreactive material. In order to investigate biocompatible properties of cinnamoyl-modified carbohydrate, hydroxypropyl cellulose (HPC) was reacted with cinnamoyl chloride to yield cinnamoyl-modified HPC (HPC-C) for
A Aĭtmambetov et al.
Bioorganicheskaia khimiia, 32(4), 446-447 (2006-08-17)
Interaction of 7-hydroxyisoflavonones with cinnamoyl chloride results in cinnamoyloxyisoflavonones.
María V Buchieri et al.
Bioorganic & medicinal chemistry letters, 23(3), 740-743 (2012-12-26)
A small series of C-cinnamoyl glycoside containing the phenol moiety was tested for the inhibition of the three Mycobacterium tuberculosis β-carbonic anhydrases (CAs, EC 4.2.1.1) with activities in the low micromolar range detected. The compounds were also tested for the
K A Connors et al.
Journal of pharmaceutical sciences, 72(4), 369-372 (1983-04-01)
The kinetics of reaction of trans-cinnamic anhydride or trans-cinnamoyl chloride with n-propyl alcohol, catalyzed by N-methylimidazole or 4-dimethylaminopyridine, were studied spectrophotometrically at 25 degrees in methyl ethyl ketone, ethylene dichloride, methylene chloride, and toluene. The acid chloride reacted in all
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