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173435-32-0

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173435-32-0 Usage

Description

3-AMINO-2-FLUORO-4-PICOLINE, also known as 2-Fluoro-4-methylpyridin-3-amine, is an organic compound with a unique molecular structure that features a fluorine atom and an amino group. It is a versatile building block in the synthesis of various pharmaceutical compounds due to its distinct chemical properties.

Uses

Used in Pharmaceutical Industry:
3-AMINO-2-FLUORO-4-PICOLINE is used as a key reactant for the synthesis of various compounds, such as phenylsulfonamidomethylbenzamides, oxopyridopyrrolopyrazinyacetamides, carbamoylalkylthiophenylmethylpicolinamides, and benzylthiotriazolylpyridines. These synthesized compounds exhibit significant structure-activity relationships (SAR) and have been found to possess both agonistic and antagonistic activities towards the kappa opioid receptor. This makes 3-AMINO-2-FLUORO-4-PICOLINE a valuable component in the development of novel therapeutic agents targeting the opioid system for pain management and other related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 173435-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 173435-32:
(8*1)+(7*7)+(6*3)+(5*4)+(4*3)+(3*5)+(2*3)+(1*2)=130
130 % 10 = 0
So 173435-32-0 is a valid CAS Registry Number.
InChI:InChI=1/F6Si.2Li/c1-7(2,3,4,5)6;;/q-2;2*+1

173435-32-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H64758)  3-Amino-2-fluoro-4-methylpyridine, 98%   

  • 173435-32-0

  • 250mg

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64758)  3-Amino-2-fluoro-4-methylpyridine, 98%   

  • 173435-32-0

  • 1g

  • 588.0CNY

  • Detail
  • Alfa Aesar

  • (H64758)  3-Amino-2-fluoro-4-methylpyridine, 98%   

  • 173435-32-0

  • 5g

  • 2352.0CNY

  • Detail

173435-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-4-methylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names 3-AMINO-2-FLUORO-4-METHYLPYRIDINE

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:173435-32-0 SDS

173435-32-0Downstream Products

173435-32-0Relevant articles and documents

N-aryl[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamide herbicides

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, (2008/06/13)

Substituted N-aryl[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide compounds, such as 5-bromo-N-(2,6-dichlorophenyl)-8-methoxy[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide, were prepared by condensation of a substituted 2-chlorosulfonyl[1,2,4]triazolo[1,5-a]pyrazine compound, such as 5-bromo-2-chlorosulfonyl-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine with a substituted arylamine compound, such as 2,6-dichloroaniline, and found to possess herbicidal utility.

Ring annulated 5-alkoxy-n-aryl[1,2,4]triazolo[1,5-C]-pyrimidine-2-sulfonamide herbicides

-

, (2008/06/13)

Substituted ring annulated 5-alkoxy-N-aryl-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide compounds, such as N-(2,6-dichlorophenyl)-5-methoxycyclopenteno[d]-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide, were prepared by condensation of an appropriate 2-chloro-sulfonyl-5-alkoxy[1,2,4]triazolo[1,5-c]pyrimidine compound, such as 2-chlorosulfonyl-5-methoxycyclopenteno[d][1,2,4]triazolo[1,5-c]pyrimidine, with a substituted arylamine compound, such as 2,6-dichloroaniline, and found to possess herbicidal utility.

N-pyridinyl[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide herbicides

-

, (2008/06/13)

Substituted N-pyridinyl[1,2,4]triazolo[1,5-c]-pyrimidine-2-sulfonamide compounds, such as N-(2-fluoro-4-methyl)-7-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide, were prepared by condensation of a 2-chlorosulfonyl[1,2,4]triazolo[1,5-c]pyrimidine compound, such as 2-chlorosulfonyl-7-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine, with a substituted 3-aminopyridine compound, such as 3-amino-2-fluoro-4-methylpyridine, and found to possess herbicidal utility.

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