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4H-Pyrazolo[3,4-d]pyrimidin-4-one, 3-amino-2,5-dihydro-6-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65919-47-3

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65919-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65919-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65919-47:
(7*6)+(6*5)+(5*9)+(4*1)+(3*9)+(2*4)+(1*7)=163
163 % 10 = 3
So 65919-47-3 is a valid CAS Registry Number.

65919-47-3SDS

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 3-amino-4-hydroxy-6-methyl-2-phenylpyrazolo<3,4-d>pyrimidine

1.2 Other means of identification

Product number -
Other names 3-amino-6-methyl-2-phenyl-2,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one

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:65919-47-3 SDS

65919-47-3Downstream Products

65919-47-3Relevant academic research and scientific papers

Synthesis of Pyrimidine Derivatives by the Reaction of Ketene Dithioacetals with Amides

Kohra, Shinya,Tominaga, Yoshinori,Hosomi, Akira

, p. 959 - 968 (2007/10/02)

Reactions of methyl 2-cyano-3,3-bis(methylthio)acrylate (1a) with carboxamides 2a-g in the presence of sodium hydride in a mixture of benzene and N,N-dimethylacetamide took place displacement with the methylthio group to give the corresponding methyl 3-N-acylamino-2-cyano-3-(methylthio)acrylates 3a-g which were readily converted to the corresponding pyrimidine derivatives at reflux in methanol in good yields.Reactions of 2-cyano-3,3-bis(methylthio)acrylonitrile (1b) with the carboxamides 2a-f gave directly pyrimidine-5-carbonitrile derivatives 7a-f.Ketene dithioacetals 1a,b smoothly reacted with thioamide 2g or urea 2h,i to give the expected pyrimidine derivatives 9,10a,b.Polyfunctionalized pyrimidines, thus obtained, were also used for the synthesis of fused pyrimidine derivatives.

Substituted pyrazolopyrimidine compounds

-

, (2008/06/13)

There are provided, as novel herbicides, the substituted pyrazolopyrimidines of the formula: STR1 where A represents -CO-NR6 - or -C(OR7)=N-, and R1, R2, R3, R4, R6 and R7 are substituent groups as defined in the specification, and the salts and acid addition salts thereof. Processes for their preparation are provided, as also are herbicidal compositions containing them and methods of combating weeds in which they are used.

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