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2-Bromo-N-(3-methoxypropyl)benzenesulphonamide is a chemical compound that belongs to the sulfonamide class of organic compounds. It is characterized by the presence of a benzene ring with a sulphonamide group, a bromine atom, and a 3-methoxypropyl substituent. 2-Bromo-N-(3-methoxypropyl)benzenesulphonamide is known for its antimicrobial and antifungal properties and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It also serves as a building block in organic synthesis and has potential applications in the development of new drugs and treatments for various diseases and conditions.

848906-56-9

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848906-56-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-N-(3-methoxypropyl)benzenesulphonamide is used as an intermediate in the synthesis of pharmaceuticals for its antimicrobial and antifungal properties. It contributes to the development of new drugs and treatments for various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Bromo-N-(3-methoxypropyl)benzenesulphonamide is utilized as an intermediate in the synthesis of agrochemicals, particularly those with antimicrobial and antifungal properties. This helps in the development of effective solutions for crop protection and management of plant diseases.
Used in Organic Synthesis:
2-Bromo-N-(3-methoxypropyl)benzenesulphonamide serves as a building block in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications. Its unique structure and functional groups make it a valuable component in the synthesis of various organic compounds.
Used in Drug Development:
2-Bromo-N-(3-methoxypropyl)benzenesulphonamide has potential use in the development of new drugs and treatments for various diseases and conditions. Its antimicrobial and antifungal properties, along with its versatility in organic synthesis, make it a promising candidate for the discovery and design of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 848906-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,9,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 848906-56:
(8*8)+(7*4)+(6*8)+(5*9)+(4*0)+(3*6)+(2*5)+(1*6)=219
219 % 10 = 9
So 848906-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BrNO3S/c1-15-8-4-7-12-16(13,14)10-6-3-2-5-9(10)11/h2-3,5-6,12H,4,7-8H2,1H3

848906-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N-(3-methoxypropyl)benzenesulfonamide

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:848906-56-9 SDS

848906-56-9Relevant academic research and scientific papers

One-pot synthesis of triazolothiadiazepine 1,1-dioxide derivatives via copper-catalyzed tandem [3+2] cycloaddition/N-arylation

Barange, Deepak Kumar,Tu, Yu-Chen,Kavala, Veerababurao,Kuo, Chun-Wei,Yao, Ching-Fa

supporting information; experimental part, p. 41 - 48 (2011/03/22)

A practical and efficient synthesis of triazolothiadiazepine-1,1-dioxide derivatives via copper-catalyzed [3+2]cycloaddition, followed by N-arylation is described. The method is also applicable to the synthesis of indoline- and thiophene-fused triazolothiadiazepine 1,1-dioxide derivatives.

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