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3-[(1E)-3,3-dimethyltriaz-1-en-1-yl]-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71609-13-7

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71609-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71609-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,0 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71609-13:
(7*7)+(6*1)+(5*6)+(4*0)+(3*9)+(2*1)+(1*3)=117
117 % 10 = 7
So 71609-13-7 is a valid CAS Registry Number.

71609-13-7SDS

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 3-(dimethylaminodiazenyl)-1-(oxan-2-yl)pyrazole-4-carboxamide

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:71609-13-7 SDS

71609-13-7Upstream product

71609-13-7Downstream Products

71609-13-7Relevant academic research and scientific papers

Synthesis and antileukemic activities of furanyl, pyranyl, and ribosyl derivatives of 4-(3,3-dimethyl-1-triazeno)imidazole-5-carboxamide and 3-(3,3-dimethyl-1-triazeno)pyrazole-4-carboxamide

Earl,Townsend

, p. 1422 - 1425 (1979)

From the reaction of silylated 4-(3,3-dimethyl-1-triazeno)imidazole-5-carboxamide (DTIC) and 3-(3,3-dimethyl-1-triazeno)pyrazole-4-carboxamide (DTPC) with 2-chlorotetrahydrofuran, we have isolated in both cases a single tetrahydrofuran-2-yl derivative. However, when silylated DTPC was reacted with 2-chlorotetrahydropyran, two tetrahydropyran-2-yl compounds were obtained, and these were shown to be positional isomers on the basis of 1H NMR and UV data. These furanyl and pyranyl derivatives were tested for antileukemic activity (L-1210, in vivo), and the results were compared with the results obtained for the corresponding ribosyl derivatives of DTIC and DTPC.

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