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364754

Sigma-Aldrich

trans-4-Nitrocinnamoyl chloride

97%

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Linear Formula:
O2NC6H4CH=CHCOCl
CAS Number:
Molecular Weight:
211.60
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

powder

mp

150-153 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(\C=C\C(Cl)=O)cc1

InChI

1S/C9H6ClNO3/c10-9(12)6-3-7-1-4-8(5-2-7)11(13)14/h1-6H/b6-3+

InChI key

RUPXNPWALFDXJD-ZZXKWVIFSA-N

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364754

trans-4-Nitrocinnamoyl chloride

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trans-4-Chloro-β-nitrostyrene

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trans-β-Styrenesulfonyl chloride

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trans-Decahydroquinoline

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

150-153 °C (lit.)

mp

112-116 °C (lit.)

mp

85-88 °C (lit.)

mp

45-50 °C

form

powder

form

solid

form

-

form

liquid

Application

trans-4-Nitrocinnamoyl chloride may be used as derivatization reagent for the analysis of perhexiline and its monohydroxy metabolite in plasma by HPLC. It may be used as derivatization reagent to investigate the in vitro enzyme kinetics and CYP isoform selectivity of perhexiline monohydroxylation using human liver microsomes.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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L B Sørensen et al.
British journal of clinical pharmacology, 55(6), 635-638 (2003-06-20)
The aims of this study were to examine the in vitro enzyme kinetics and CYP isoform selectivity of perhexiline monohydroxylation using human liver microsomes. Conversion of rac-perhexiline to monohydroxyperhexiline by human liver microsomes was assessed using a high-performance liquid chromatography
N Grgurinovich
Journal of chromatography. B, Biomedical sciences and applications, 696(1), 75-80 (1997-08-15)
A high-performance liquid chromatographic method for the analysis of perhexiline and its monohydroxy metabolite in plasma has been developed. After a simple extraction procedure, the analytes are derivatized over a 30-min period with trans-4-nitrocinnamoyl chloride. The derivatized products are monitored

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