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6-Bromo-pyridine-3-sulfonyl chloride, also known as Bpys-Cl, is a chemical compound with the molecular formula C5H3BrClNOS. It is a sulfonamide derivative featuring a bromo-pyridine core, which is widely recognized for its reactivity with nucleophiles and its capacity to form covalent bonds with various substrates. 6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is a valuable building block in the synthesis of pharmaceuticals and agrochemicals, and it has been extensively studied for its potential applications in medicinal chemistry, particularly in the development of innovative therapeutic agents. Furthermore, Bpys-Cl serves as a reagent in organic synthesis, especially in the construction of heterocyclic compounds. It is a versatile chemical reagent with significant applications in the realms of chemical and pharmaceutical research.

886371-20-6

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886371-20-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals due to its reactivity with nucleophiles and its ability to form covalent bonds with a range of substrates. This property makes it a key component in the development of new drugs and pesticides.
Used in Medicinal Chemistry Research:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a reagent in medicinal chemistry research for the development of novel therapeutic agents. Its unique chemical structure and reactivity contribute to the creation of innovative compounds with potential therapeutic applications.
Used in Organic Synthesis:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a reagent in organic synthesis, particularly for the construction of heterocyclic compounds. Its versatility in forming covalent bonds with different substrates makes it an essential tool in the synthesis of complex organic molecules.
Used in Chemical Research:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is utilized in chemical research to explore its reactivity and potential applications in various chemical reactions. Its unique properties allow researchers to investigate new pathways and mechanisms in chemical synthesis and compound development.

Check Digit Verification of cas no

The CAS Registry Mumber 886371-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 886371-20:
(8*8)+(7*8)+(6*6)+(5*3)+(4*7)+(3*1)+(2*2)+(1*0)=206
206 % 10 = 6
So 886371-20-6 is a valid CAS Registry Number.

886371-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromopyridine-3-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names I02-2840

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:886371-20-6 SDS

886371-20-6Downstream Products

886371-20-6Relevant articles and documents

Efficient and scalable synthesis of pyridine sulfonamides

Emura, Takashi,Yoshino, Hitoshi,Tachibana, Kazutaka,Shiraishi, Takuya,Honma, Akie,Mizutani, Akemi,Muraoka, Terushige

experimental part, p. 1117 - 1120 (2011/06/20)

Short-step and scalable transformations from 2,6-dibromopyridine to 6-bromopyridine-2-sulfonamide by means of halogen-metal exchange and subsequent reaction with sulfuryl chloride followed by amidation are established. Application of the method for the synthesis of various pyridine sulfonamides is also described. Georg Thieme Verlag Stuttgart - New York.

BI-ARYL AMINOTETRALINES

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Page/Page column 18, (2010/03/04)

The invention is concerned with the compounds of formula I: and pharmaceutically acceptable salts and esters thereof, wherein R1-R5, A, B, Q, W, and X are defined in the detailed description and claims. In addition, the present invention relates to methods of manufacturing and using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds of formula I are antagonists at the CRTH2 receptor and may be useful in treating diseases and disorders associated with that receptor such as asthma.

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