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Propanedioic acid, (1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62141-13-3

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62141-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62141-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,4 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62141-13:
(7*6)+(6*2)+(5*1)+(4*4)+(3*1)+(2*1)+(1*3)=83
83 % 10 = 3
So 62141-13-3 is a valid CAS Registry Number.

62141-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-phenyl-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-ylidene)malonic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 2-(1-Phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-malonic acid diethyl ester

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:62141-13-3 SDS

62141-13-3Downstream Products

62141-13-3Relevant academic research and scientific papers

Antimicrobial Activity of Amino Acid, Imidazole, and Sulfonamide Derivatives of Pyrazolo[3,4-d]pyrimidine

Ghorab,Ismail, Zeinab H.,Abdel-Gawad, Soad M.,Aziem, Anhar Abdel

, p. 57 - 62 (2004)

Derivatives of pyrazolo[3,4-d]pyrimidine with amino acid 3a-d, imidazole 4a-d, carbonyl 6-9, pyrazole 10, pyrazolone 11, and sulfonamide 12-17 moieties were synthesized. Structure of the new compounds were established by their elemental analyses and spectral data. Some of the synthesized compounds were tested in vitro for their antimicrobial activity. Compounds 4b, 12, and 16 were almost as potent as the standard antibiotic Chloramphenicol as positive control. Also, compounds 3b, 3c, 12, and 16 were nearly as active as Terbinafine as positive control.

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