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1H-Pyrazolo[3,4-d]pyrimidine, 4,6-bis(methylthio)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129852-43-3

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129852-43-3 Usage

Molecular Structure

1H-Pyrazolo[3,4-d]pyrimidine, 4,6-bis(methylthio)-3-phenylhas a complex molecular structure that belongs to the pyrazolo[3,4-d]pyrimidine family.

Methylthio Groups

It contains two methylthio groups at positions 4 and 6.

Phenyl Group

It has a phenyl group at position 3.

Medicinal Chemistry

The compound is of interest in medicinal chemistry and pharmaceutical research due to its potential biological activities.

Drug Development

It may have applications in drug development and discovery, particularly in the field of cancer and other diseases.

Further Research

Further studies and research are needed to fully understand and exploit the potential of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 129852-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,5 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 129852-43:
(8*1)+(7*2)+(6*9)+(5*8)+(4*5)+(3*2)+(2*4)+(1*3)=153
153 % 10 = 3
So 129852-43-3 is a valid CAS Registry Number.

129852-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Bis(methylthio)-3-phenylpyrazolo<3,4-d>pyrimidine

1.2 Other means of identification

Product number -
Other names 4,6-Bis-methylsulfanyl-3-phenyl-1H-pyrazolo[3,4-d]pyrimidine

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:129852-43-3 SDS

129852-43-3Relevant academic research and scientific papers

Polarized Ethylenes. IV. Synthesis of Polarized Ethylenes Using Thioamides and Methyl Dithiocarboxylates and their Application to Syntheses of Pyrazoles, Pyrimidines, Pyrazolopyrimidines, and 5-Azacyclazines

Tominaga, Yoshinori,Matsuoka, Yoshiki,Oniyama, Yukio,Uchimura, Yoshimitsu,Komiya, Hirofumi,et al.

, p. 647 - 660 (2007/10/02)

Polarized ethylenes having both electron-donating (an amino or a methylthio group) and electron-accepting (cyano, carbamoyl, methyl ester) groups on the adjacent two olefinic carbon atoms were prepared by the condensation of S-alkylthioamidinium salts or

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