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13297-36-4

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13297-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13297-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13297-36:
(7*1)+(6*3)+(5*2)+(4*9)+(3*7)+(2*3)+(1*6)=104
104 % 10 = 4
So 13297-36-4 is a valid CAS Registry Number.

13297-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-Dimethyl-3-propyl-3,7-dihydro-purin-2,6-dion

1.2 Other means of identification

Product number -
Other names 1,7-dimethyl-3-propyl-3,7-dihydro-purine-2,6-dione

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:13297-36-4 SDS

13297-36-4Relevant articles and documents

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Morrison

, p. 4483 (1954)

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Cobalt-Catalyzed Sustainable Synthesis of Benzimidazoles by Redox-Economical Coupling of o-Nitroanilines and Alcohols

Das, Sanju,Mallick, Samrat,De Sarkar, Suman

, p. 12111 - 12119 (2019/10/02)

This study reveals cobalt-catalyzed sustainable synthesis of benzimidazoles by redox-economical coupling of o-nitroanilines and alcohols. The major advantage of this report is the use of a commercially available cheap cobalt catalyst to produce a wide variety of 2-substituted benzimidazoles by hydrogen autotransfer without using any additional external redox reagent and costly ligand system. A thorough mechanistic insight of the reaction is proposed by performing a series of control experiments.

Design, synthesis, and biological activities of new thieno[3,2- d]pyrimidines as selective type 4 phosphodiesterase inhibitors

Crespo, Maria I.,Pagès, Lluís,Vega, Armando,Segarra, Victor,López, Manel,Doménech, Teresa,Miralpeix, Montserrat,Beleta, Jordi,Ryder, Hamish,Palacios, José M.

, p. 4021 - 4035 (2007/10/03)

A common pharmacophore for compounds structurally related to nitraquazone has been derived. Using this pharmacophore, new structures have been designed, synthesized, and evaluated for their inhibitory potencies against cyclic adenosine 5'-monophosphate (c

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