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28177-14-2

5-(3-(2-chloroethyl)triazen-1-yl)imidazole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28177-14-2

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28177-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28177-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,7 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28177-14:
(7*2)+(6*8)+(5*1)+(4*7)+(3*7)+(2*1)+(1*4)=122
122 % 10 = 2
So 28177-14-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H9ClN6O/c7-1-2-11-13-12-6-4(5(8)14)9-3-10-6/h3,11,13H,1-2H2,(H2,8,14)/b12-6+

28177-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Imidazole-4-carboxamide, 5-[3-(2-chloroethyl)-1-triazenyl ]-

1.2 Other means of identification

Product number -
Other names 5-(3-(2-chloroethyl)triazen-1-yl)imidazole-4-carboxamide

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:28177-14-2 SDS

28177-14-2Upstream product

28177-14-2Downstream Products

28177-14-2Relevant articles and documents

Antitumor Imidazotetrazines. 1. Synthesis and Chemistry of 8-Carbamoyl-3-(2-chloroethyl)imidazo-1,2,3,5-tetrazin-4(3H)-one, a Novel Broad-Spectrum Antitumor Agent

Stevens, Malcolm F. G.,Hickman, John A.,Stone, Robert,Gibson, Neil W.,Baig, Ghouse Unissa,et al.

, p. 196 - 201 (2007/10/02)

Interaction of 5-diazoimidazole-4-carboxamide and alkyl and aryl isocyanates in the dark affords 8-carbamoyl-3-substituted-imidazo-1,2,3,5-tetrazin-4(3H)-ones.In cold methanol or ethanol, the 3-(2-chloroethyl) derivative 7a decomposes to afford 2-azahypoxanthine (14) and methyl and ethyl N-(2-chloroethyl)carbamates, respectively.Compound 7a has curative activity against L-1210 and P388 leukemia and may act as a prodrug modification of the acyclic triazene 5-imidazole-4-carboxamide (MCTIC), since it ring opens to form the triazene in aqueous sodium carbonate.

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