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C81101

Sigma-Aldrich

Cinnamoyl chloride

new

≥95.0%

Synonym(s):

trans-3-Phenylacryloyl chloride

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About This Item

Linear Formula:
C6H5CH=CHCOCl
CAS Number:
102-92-1
Molecular Weight:
166.60
Beilstein:
606265
EC Number:
203-065-5
MDL number:
MFCD00000732
UNSPSC Code:
12352100
PubChem Substance ID:
24893025
NACRES:
NA.22

Assay

≥95.0%

form

solid

bp

256-258 °C (lit.)

mp

35-37 °C (lit.)

storage temp.

2-8°C

SMILES string

ClC(=O)\C=C\c1ccccc1

InChI

1S/C9H7ClO/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H/b7-6+

InChI key

WOGITNXCNOTRLK-VOTSOKGWSA-N

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Related Categories

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Methyl cinnamate ≥99.0% (GC)

Sigma-Aldrich

96410

Methyl cinnamate

4-Chlorocinnamic acid 99%

Sigma-Aldrich

C31600

4-Chlorocinnamic acid

Yukiya Kitayama et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(52), 12870-12875 (2017-06-29)
In this study, a fabrication route towards functional capsule particles was successfully developed by means of a self-templating shell-selective cross-linking strategy that enables us to prepare shell-cross-linked hollow polymer particles directly from homogeneous spherical polymer particles. To prepare redox-responsive degradable
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
A Aĭtmambetov et al.
Bioorganicheskaia khimiia, 32(4), 446-447 (2006-08-17)
Interaction of 7-hydroxyisoflavonones with cinnamoyl chloride results in cinnamoyloxyisoflavonones.
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
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
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