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957760-15-5

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957760-15-5 Usage

General Description

7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine is a chemical compound with the molecular formula C8H6ClN3. It is a heterocyclic compound containing a pyrazole and pyridine ring fused together. 7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine is used in the pharmaceutical industry as a building block in the synthesis of various drugs and bioactive compounds. It is also known to exhibit biological activities such as antifungal and antibacterial properties. Additionally, 7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine has potential applications in the development of new pharmacological agents and agrochemicals due to its unique structure and properties. However, further research and studies are required to fully understand its potential uses and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 957760-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,7,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 957760-15:
(8*9)+(7*5)+(6*7)+(5*7)+(4*6)+(3*0)+(2*1)+(1*5)=215
215 % 10 = 5
So 957760-15-5 is a valid CAS Registry Number.

957760-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrazolo[3,4-c]pyridine, 7-chloro-1-methyl-

1.2 Other means of identification

Product number -
Other names 7-CHLORO-1-METHYL-1H-PYRAZOLO[3,4-C]PYRIDINE

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:957760-15-5 SDS

957760-15-5Downstream Products

957760-15-5Relevant articles and documents

Carbocyclic 4-deazaformycins

Zhang, Yan,Ye, Wei,Wang, Haisheng,Schneller, Stewart W.

, p. 723 - 730 (2012)

The preparation of carbocyclic 4-deazaformycin and its 5-homoanalogue from a common vinyl precursor, and its N-1 and N-2 methyl derivatives is reported. The syntheses began with a highly stereoselective SN2 reaction between lithio 4-picolines and a protected 2,3-dihydroxy-4-vinylcyclopentyl triflate. The requisite fused pyrazole ring was created by an intramolecular diazonium reaction that was followed by vinyl transformation into the hydroxymethyl and the hydroxyethyl groups. The N-methyl derivatives arose by standard methylation conditions and the resultant N-Me regiochemistry was assigned by homo- and heteronuclear NMR spectroscopy. Georg Thieme Verlag Stuttgart · New York.

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