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Sulfamide, N-(2-chloroethyl)-N',N'-dicyclohexyl-N-nitroso- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182925-76-4

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182925-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182925-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,9,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182925-76:
(8*1)+(7*8)+(6*2)+(5*9)+(4*2)+(3*5)+(2*7)+(1*6)=164
164 % 10 = 4
So 182925-76-4 is a valid CAS Registry Number.

182925-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chloroethyl)-N-(dicyclohexylsulfamoyl)nitrous amide

1.2 Other means of identification

Product number -
Other names -

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:182925-76-4 SDS

182925-76-4Relevant academic research and scientific papers

A new family of potential oncostatics: 2-Chloroethylnitrososulfamides (CENS) - I. Synthesis, structure, and pharmacological evaluation (preliminary results)

Abdaoui, Mohamed,Dewynter, Georges,Aouf, Nourredine,Favre, Gilles,Morere, Alain,Montero, Jean-Louis

, p. 1227 - 1235 (2007/10/03)

A new series of alkylating agents, 2-chloroethylnitrososulfamides (CENS), were developed on the model of 2-chloroethylnitrosoureas. Starting from chlorosulfonyl isocyanate, a four-step synthesis (carbamoylation-sulfamoylation, Mitsunobu alkylation, deprotection, and nitrosation) gives the title compounds in a 47-58% overall yield. The selection of the nitrosation site can be directed through an alternative route. The pharmacological evaluation shows a significant oncostatic activity towards both A549 and MCF7 cell lines.

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