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2H-Pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione, 2-(diphenylamino)-5,7-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89549-96-2

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89549-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89549-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,4 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89549-96:
(7*8)+(6*9)+(5*5)+(4*4)+(3*9)+(2*9)+(1*6)=202
202 % 10 = 2
So 89549-96-2 is a valid CAS Registry Number.

89549-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Diphenylamino-5,7-dimethyl-2,7-dihydro-pyrazolo[3,4-d]pyrimidine-4,6-dione

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:89549-96-2 SDS

89549-96-2Downstream Products

89549-96-2Relevant academic research and scientific papers

Pyrimidine Derivatives and Related Compounds. XLVI. Thermal and Photochemical Transformation of 5-Substituted 6-Azido-1,3-dimethyluracils into Fused Pyrimidines such as Isoxazolopyrimidines, Pyrazolo-pyrimidines, and Pyrimido-t

Hirota, Kosaku,Maruhashi, Kazuo,Asao, Tetsuji,Kitamura, Norihiko,Maki, Yoshifumi,Senda, Shigeo

, p. 3959 - 3966 (2007/10/02)

Thermolysis and photolysis of 6-azido-1,3-dimethyluracils possessing certain substituents (formyl, benzoyl, hydrazonomethyl, phenyl, and benzyl groups) at the 5-position provided new methods for the preparation of fused pyrimidines.Irradiation and heating

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