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873107-98-3

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873107-98-3 Usage

Description

5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE is an organic compound characterized by the presence of an iodine atom at the 5-position and a trifluoromethyl group at the 2-position on a pyridine ring. This unique molecular structure endows it with specific reactivity and properties, making it a valuable intermediate in various chemical synthesis processes.

Uses

Used in Pharmaceutical Industry:
5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to participate in metal-catalyzed organic reactions. This allows for the creation of new drug molecules with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE serves as a versatile reactant for exploring novel metal-catalyzed organic reactions. Its reactivity and structural features facilitate the development of new synthetic pathways and methodologies, contributing to the advancement of organic chemistry.
Used in Material Science:
5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE is utilized in the development of new materials with specific properties, such as those with potential applications in electronics, coatings, or other high-tech industries. Its unique structure allows for the creation of materials with tailored characteristics through metal-catalyzed organic reactions.
Used in Agrochemical Industry:
5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE is employed as a building block in the synthesis of agrochemicals, including pesticides and herbicides. Its involvement in metal-catalyzed organic reactions enables the production of new compounds with improved efficacy and selectivity in agricultural applications.
Overall, 5-IODO-2-(TRIFLUOROMETHYL)PYRIDINE is a significant compound in various industries due to its role as a reactant in metal-catalyzed organic reactions, which allows for the synthesis of a wide range of products with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 873107-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,1,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 873107-98:
(8*8)+(7*7)+(6*3)+(5*1)+(4*0)+(3*7)+(2*9)+(1*8)=183
183 % 10 = 3
So 873107-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F3IN/c7-6(8,9)5-2-1-4(10)3-11-5/h1-3H

873107-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Iodo-2-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names -

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:873107-98-3 SDS

873107-98-3Relevant articles and documents

Rapid Assembly of Saturated Nitrogen Heterocycles in One-Pot: Diazo-Heterocycle “Stitching” by N–H Insertion and Cyclization

Boddy, Alexander J.,Affron, Dominic P.,Cordier, Christopher J.,Rivers, Emma L.,Spivey, Alan C.,Bull, James A.

supporting information, p. 1458 - 1462 (2019/01/04)

Methods that provide rapid access to new heterocyclic structures in biologically relevant chemical space provide important opportunities in drug discovery. Here, a strategy is described for the preparation of 2,2-disubstituted azetidines, pyrrolidines, pi

DIFLUOROETHYLPYRIDINE DERIVATIVES AS NR2B NMDA RECEPTOR ANTAGONISTS

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Paragraph 0251, (2016/02/16)

Disclosed are chemical entities of formula (I) wherein X, Y, Z, R1, R3, R4, R5 and R6 are defined herein, as NR2B subtype selective receptor antagonists. Also disclosed are pharmaceutical compositions comprising a chemical entity of formula (I), and methods of treating various diseases and disorders associated with NR2B antagonism, e.g., diseases and disorders of the CNS, such as depression, by administering a chemical entity of formula I.

COMPOUNDS

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Page/Page column 25, (2010/02/15)

The invention provides compounds of formula (I): wherein R1 and R2 are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the pharmaceutical compositions; and their use in therapy.

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