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363871

4-Chlorophenyl chloroformate

Name: 4-Chlorophenyl chloroformate
Brand: ALDRICH

98%

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About This Item

Linear Formula:

ClCO₂C₆H₄Cl

CAS Number:

7693-45-0

Molecular Weight:

191.01

NACRES:

NA.22

PubChem Substance ID:

24862369

UNSPSC Code:

12352100

MDL number:

MFCD00000638

Assay:

98%

Form:

liquid

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Properties

assay

98%

form

liquid

refractive index

n20/D 1.533 (lit.)

bp

100-102 °C/12 mmHg (lit.)

density

1.365 g/mL at 25 °C (lit.)

functional group

chloro

storage temp.

2-8°C

SMILES string

ClC(=O)Oc1ccc(Cl)cc1

InChI

1S/C7H4Cl2O2/c8-5-1-3-6(4-2-5)11-7(9)10/h1-4H

InChI key

RYWGPCLTVXMMHO-UHFFFAOYSA-N

Description

Application

4-Chlorophenyl chloroformate was used in the preparation of N-hydroxy-N-methylcarbamate 4-chlorophenyl ester.

pictograms

GHS06,GHS05

signalword

Danger

hcodes

H301 + H311 + H331,H314

pcodes

P261 - P271 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

217.4 °F - closed cup

flash_point_c

103 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Inhibition of glyoxalase I by the enediol mimic S-(N-hydroxy-N-methylcarbamoyl)glutathione. The possible basis of a tumor-selective anticancer strategy.

D S Hamilton et al.

The Journal of biological chemistry, 267(35), 24933-24936 (1992-12-15)

In principle, competitive inhibitors of glyoxalase I that also serve as substrates for the thioester hydrolase glyoxalase II might function as tumor-selective anti-cancer agents, given the role of these enzymes in removing cytotoxic methylglyoxal from cells and the observation that

Global Trade Item Number

SKU	GTIN
363871-5G	04061836684716