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C81101

Sigma-Aldrich

Cinnamoyl chloride

new

≥95.0%

Sinônimo(s):

trans-3-Phenylacryloyl chloride

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About This Item

Fórmula linear:
C6H5CH=CHCOCl
Número CAS:
102-92-1
Peso molecular:
166.60
Beilstein:
606265
Número CE:
203-065-5
Número MDL:
MFCD00000732
Código UNSPSC:
12352100
ID de substância PubChem:
24893025
NACRES:
NA.22

Ensaio

≥95.0%

forma

solid

pb

256-258 °C (lit.)

pf

35-37 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

ClC(=O)\C=C\c1ccccc1

InChI

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

chave InChI

WOGITNXCNOTRLK-VOTSOKGWSA-N

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Categorias relacionadas

Pictogramas

Corrosion
GHS05

Palavra indicadora

Danger

Frases de perigo

H314

Classificações de perigo

Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análise (COA)

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p-Coumaroyl alcohol phyproof® Reference Substance

PHL82506

p-Coumaroyl alcohol

Methyl cinnamate ≥99.0% (GC)

Sigma-Aldrich

96410

Methyl cinnamate

4-Chlorocinnamic acid 99%

Sigma-Aldrich

C31600

4-Chlorocinnamic acid

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.
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
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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