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6-CHLORO-2-METHYLPYRIDINE-3-SULFONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

889944-74-5

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889944-74-5 Usage

General Description

6-chloro-2-methylpyridine-3-sulfonyl chloride is a chemical compound that belongs to the class of sulfonyl chlorides, which are commonly used as reagents in organic synthesis. 6-chloro-2-methylpyridine-3-sulfonyl chloride is characterized by a chlorinated pyridine ring with a sulfonyl chloride moiety attached at the 3-position and a methyl group at the 2-position. It is commonly used in the pharmaceutical industry as a building block in the synthesis of various pharmaceutical compounds. Additionally, it has applications in the field of agrochemicals and material science. The sulfonyl chloride functionality in 6-chloro-2-methylpyridine-3-sulfonyl chloride makes it a versatile reagent for the introduction of sulfonamide groups in organic molecules, making it an important intermediate in synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 889944-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,9,4 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 889944-74:
(8*8)+(7*8)+(6*9)+(5*9)+(4*4)+(3*4)+(2*7)+(1*4)=265
265 % 10 = 5
So 889944-74-5 is a valid CAS Registry Number.

889944-74-5Downstream Products

889944-74-5Relevant academic research and scientific papers

TRIAZOLOPYRIDINE COMPOUNDS AND METHODS FOR THE TREATMENT OF CYSTIC FIBROSIS

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Paragraph 0120; 0121, (2016/05/02)

The invention relates to a compound of Formula I or IA and methods of treating cystic fibrosis comprising the step of administering a therapeutically effective amount of a compound of Formula I or IA to a patient in need thereof:

Acid secretion inhibitor

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Page/Page column 39, (2008/06/13)

The present invention provides a compound having a superior acid secretion inhibitory effect and showing an antiulcer activity and the like. The present invention provides a compound represented by the formula (I) wherein R1 is a nitrogen-containing monocyclic heterocyclic group optionally condensed with a benzene ring or a heterocycle, the nitrogen-containing monocyclic heterocyclic group optionally condensed with a benzene ring or a heterocycle optionally has substituent(s), R2 is an optionally substituted C6-14 aryl group, an optionally substituted thienyl group or an optionally substituted pyridyl group, R3 and R4 are each a hydrogen atom, or one of R3 and R4 is a hydrogen atom and the other is an optionally substituted lower alkyl group, an acyl group, a halogen atom, a cyano group or a nitro group, and R5 is an alkyl group or a salt thereof.

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