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Merck
CN

364754

反式-4-硝基肉桂酰氯

97%

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线性分子式:
O2NC6H4CH=CHCOCl
化学文摘社编号:
分子量:
211.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

反式-4-硝基肉桂酰氯, 97%

InChI

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

SMILES string

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

InChI key

RUPXNPWALFDXJD-ZZXKWVIFSA-N

assay

97%

form

powder

mp

150-153 °C (lit.)

functional group

acyl chloride
nitro

Quality Level

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

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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

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