Merck
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C81101

Sigma-Aldrich

Cinnamoyl chloride

≥95.0%

Sinônimo(s):
trans-3-Phenylacryloyl chloride
Fórmula linear:
C6H5CH=CHCOCl
Número CAS:
Peso molecular:
166.60
Beilstein:
606265
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.22

teor

≥95.0%

forma

solid

pb

256-258 °C (lit.)

pf

35-37 °C (lit.)

temperatura de armazenamento

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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Categorias relacionadas

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Ponto de fulgor (ºF)

235.4 °F - closed cup

Ponto de fulgor (ºC)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges

Certificado de análise

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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
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

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