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3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE is a heterocyclic organic compound characterized by the molecular formula C8H6IN3. It integrates nitrogen and iodine atoms within its structure, making it a significant building block in the synthesis of pharmaceuticals and agrochemicals. 3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE also exhibits potential biological activities and has been a subject of interest for drug development due to its possible role as an enzyme and receptor inhibitor in the human body. However, it is crucial to handle 3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE with care, given its potentially hazardous nature.

685522-76-3

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685522-76-3 Usage

Uses

Used in Pharmaceutical Industry:
3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of molecules with specific biological activities, making it a valuable asset in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE is utilized as a precursor in the production of agrochemicals, potentially leading to the development of novel pesticides or other agricultural chemicals that can improve crop protection and yield.
Used in Drug Development:
3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE is employed as a compound of interest in drug development due to its potential biological activities. Researchers are investigating its capacity to inhibit certain enzymes and receptors, which could lead to the discovery of new therapeutic agents for various diseases.
Used as an Enzyme and Receptor Inhibitor:
3-IODO-1-METHYL-1H-PYRAZOLO[3,4-B]PYRIDINE is studied for its potential role as an inhibitor of specific enzymes and receptors in the human body. This application is crucial in the development of targeted therapies for conditions where enzyme or receptor modulation can have a therapeutic effect.

Check Digit Verification of cas no

The CAS Registry Mumber 685522-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,5,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 685522-76:
(8*6)+(7*8)+(6*5)+(5*5)+(4*2)+(3*2)+(2*7)+(1*6)=193
193 % 10 = 3
So 685522-76-3 is a valid CAS Registry Number.

685522-76-3SDS

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 3-iodo-1-methylpyrazolo[3,4-b]pyridine

1.2 Other means of identification

Product number -
Other names 3-iodo-1-methyl-1Hpyrazolo[3,4-b]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:685522-76-3 SDS

685522-76-3Relevant articles and documents

Palladium-catalyzed aminocarbonylation of halo-substituted 7-azaindoles and other heteroarenes using chloroform as a carbon monoxide source

Kannaboina, Prakash,Raina, Gaurav,Anil Kumar,Das, Parthasarathi

supporting information, p. 9446 - 9449 (2017/09/01)

A palladium-catalyzed aminocarbonylation of halo-substituted 7-azaindoles utilizing CHCl3 as the carbonyl source has been developed for the straightforward incorporation of an amide functional group. The protocol was extended to other heteroarenes such as pyrazolopyridines and indazoles. The substrate scope of the reaction with respect to heteroarenes and the amine component is reported. This method offers an alternative avenue for aminocarbonylation of pharmaceutically important heterocycles.

Synthesis and functionalisation of 1H-pyrazolo[3,4-b]pyridines involving copper and palladium-promoted coupling reactions

Lavecchia,Berteina-Raboin,Guillaumet

, p. 2389 - 2392 (2007/10/03)

A convenient route to novel 3-iodo-1H-pyrazolo[3,4-b]pyridines via iododediazonation of 3-amino-1H-pyrazolo[3,4-b]pyridines, which are obtained by copper-catalysed cyclisation of 2-chloro-3-cyanopyridine with hydrazines. We describe also efficient couplin

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