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2-chloroethyl N-hydroxycarbamate, also known as bis(2-chloroethyl) N-hydroxycarbamate or uracil mustard, is a chemical compound with the molecular formula C4H8Cl2N2O2. It is a halogenated nitrogen mustard, which is a type of alkylating agent used in chemotherapy to treat various types of cancer, including lymphomas and leukemia. The compound works by forming covalent bonds with DNA, causing cross-linking and preventing DNA replication, ultimately leading to cell death. Due to its cytotoxic nature, it is crucial to handle 2-chloroethyl N-hydroxycarbamate with extreme caution and in a controlled environment to minimize exposure risks.

7162-18-7

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7162-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7162-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7162-18:
(6*7)+(5*1)+(4*6)+(3*2)+(2*1)+(1*8)=87
87 % 10 = 7
So 7162-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H6ClNO3/c4-1-2-8-3(6)5-7/h7H,1-2H2,(H,5,6)

7162-18-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl N-hydroxycarbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,hydroxy-,2-chloroethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7162-18-7 SDS

7162-18-7Downstream Products

7162-18-7Relevant academic research and scientific papers

α-Nitrosostyrenes as Three-Atom Units for the (3+1) Cyclization Reaction: Facile Access to 2,3-Dihydrodiazete N-Oxides and Their Diversified Synthetic Conversions

Shen, Li-Wen,Wang, Zhen-Hua,You, Yong,Yuan, Wei-Cheng,Zhao, Jian-Qiang,Zhou, Ming-Qiang

supporting information, p. 1094 - 1099 (2022/02/10)

An unprecedented (3+1) cyclization of α-nitrosostyrenes, generated in situ from α-bromooximes, and N-tosyloxycarbamates was developed, which enables the synthesis of a range of structurally unique and hitherto unexplored 2,3-dihydrodiazete N-oxides in mod

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