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77332-79-7

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77332-79-7 Usage

Description

3-Chloro-4-iodopyridine is an organic compound with the molecular formula C5H3ClIN. It is a heterocyclic compound featuring a pyridine ring with a chlorine atom at the 3rd position and an iodine atom at the 4th position. 3-CHLORO-4-IODOPYRIDINE is known for its reactivity and is commonly utilized as a building block in the synthesis of various pharmaceuticals and chemical compounds.

Uses

Used in Pharmaceutical Industry:
3-Chloro-4-iodopyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for further functionalization and modification, making it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-chloro-4-iodopyridine serves as a versatile building block for the creation of a wide range of compounds. Its reactivity with different reagents enables the formation of various derivatives, which can be used in different applications, such as agrochemicals, dyes, and other specialty chemicals.
Used in the Preparation of Difluoromethylated Pyridines:
3-Chloro-4-iodopyridine is used as a starting material for the preparation of difluoromethylated pyridines. These compounds are of interest due to their potential applications in various fields, including pharmaceuticals and materials science.
Used in the Synthesis of 5-Chloro-4-(trifluoromethyl)-2-pyridinecarboxylic Acid (C421715):
3-Chloro-4-iodopyridine is also an intermediate in the synthesis of 5-chloro-4-(trifluoromethyl)-2-pyridinecarboxylic acid (C421715), a compound with potential applications in the development of new drugs and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 77332-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77332-79:
(7*7)+(6*7)+(5*3)+(4*3)+(3*2)+(2*7)+(1*9)=147
147 % 10 = 7
So 77332-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClIN/c6-4-3-8-2-1-5(4)7/h1-3H

77332-79-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H63866)  3-Chloro-4-iodopyridine, 97%   

  • 77332-79-7

  • 1g

  • 529.0CNY

  • Detail
  • Alfa Aesar

  • (H63866)  3-Chloro-4-iodopyridine, 97%   

  • 77332-79-7

  • 5g

  • 1784.0CNY

  • Detail
  • Aldrich

  • (724114)  3-Chloro-4-iodopyridine  97%

  • 77332-79-7

  • 724114-1G

  • 749.97CNY

  • Detail

77332-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-Iodopyridine

1.2 Other means of identification

Product number -
Other names 3-CHLORO-4-IODOPYRIDINE

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:77332-79-7 SDS

77332-79-7Upstream product

77332-79-7Relevant articles and documents

TRIAZOLONE COMPOUNDS AS mPGES-1 INHIBITORS

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Page/Page column 61; 62, (2014/01/08)

The present disclosure is directed to compounds of formula (I), and pharmaceutically acceptable salts thereof, as mPGES-1 inhibitors. These compounds are inhibitors of the microsomal prostaglandin E synthase-1 (mPGES-1) enzyme and are therefore useful in the treatment of pain and/or inflammation from a variety of diseases or conditions, such as asthma, osteoarthritis, rheumatoid arthritis, acute or chronic pain and neurodegenerative diseases.

Palladium-catalyzed aryl amination-heck cyclization cascade: A one-flask approach to 3-substituted indoles

Jensen, Thomas,Pedersen, Henrik,Bang-Andersen, Benny,Madsen, Robert,Jorgensen, Morten

, p. 888 - 890 (2008/09/20)

(Chemical Equation Presented) Two for the price of one: A Pd/dppf-based catalyst provides access to the title compounds from 1,2-dihalogenated aromatic compounds and allylic amines in a single reaction flask. The initial aryl amination step occurs with excellent selectivity for the aryl iodide to ensure the formation of a single indole regioisomer, which can be functionalized in situ by N-arylation (see scheme). dba = dibenzylideneacetone, dppf = 1,1′-bis(diphenylphospanyl)ferrocene.

GLYCINE TRANSPORTER INHIBITOR

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Page/Page column 108-109, (2010/11/30)

The present invention provides a compound represented by the following formula or a pharmaceutically acceptable salt of the compound or a hydrate of the compound or the salt, which is useful for the prevention or treatment of diseases such as schizophreni

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