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1202704-57-1

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1202704-57-1 Usage

Description

(1,2-diamino-5-bromopyridin-1-ium) 2,4,6-trimethylbenzenesulfonate is a salt molecule that consists of a bromopyridinium cation and a 2,4,6-trimethylbenzenesulfonate anion. It is characterized by the presence of two amino groups and a bromine atom attached to a pyridine ring in the cation, while the anion is a sulfonate derivative of toluene. This chemical compound is frequently utilized in organic synthesis as a reagent or catalyst and has applications in pharmaceutical research and development.

Uses

Used in Organic Synthesis:
(1,2-diamino-5-bromopyridin-1-ium) 2,4,6-trimethylbenzenesulfonate is used as a reagent or catalyst in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, (1,2-diamino-5-bromopyridin-1-ium) 2,4,6-trimethylbenzenesulfonate is used as a compound in research and development. Its unique structure and properties make it a candidate for the design and synthesis of new drugs.
Used in Antibacterial Applications:
(1,2-diamino-5-bromopyridin-1-ium) 2,4,6-trimethylbenzenesulfonate has been studied for its potential biological activity and has shown promise as an antibacterial agent, making it a candidate for the development of new antibiotics to combat bacterial infections.
Used in Antifungal Applications:
Similarly, this compound has demonstrated potential as an antifungal agent, indicating its use in the development of treatments for fungal infections.
Used in Neurological Disorder Treatment:
(1,2-diamino-5-bromopyridin-1-ium) 2,4,6-trimethylbenzenesulfonate has also been investigated for its potential as a treatment for certain neurological disorders, suggesting its use in the medical field for addressing such conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1202704-57-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,7,0 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1202704-57:
(9*1)+(8*2)+(7*0)+(6*2)+(5*7)+(4*0)+(3*4)+(2*5)+(1*7)=101
101 % 10 = 1
So 1202704-57-1 is a valid CAS Registry Number.

1202704-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diamino-5-bromo-pyridinium 2,4,6-trimethyl-benzenesulfonate

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:1202704-57-1 SDS

1202704-57-1Relevant articles and documents

4-QUINOLINONE ANTIBACTERIAL COMPOUNDS

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Page/Page column 30; 31, (2021/04/10)

The present invention relates to the following compounds (I) wherein the integers are as defined in the description, and where the compounds may be useful as medicaments, for instance for use in the treatment of tuberculosis (e.g. in combination).

OXAZOLIDINONE DERIVATIVE HAVING FUSED RING

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Page/Page column 58, (2011/05/05)

The present invention provides a novel antimicrobial drug comprising an oxazolidinone derivative of the formula (I): or a pharmaceutically acceptable salt or solvate thereof; wherein ring A is ring B is a benzene ring optionally substituted with lower alkyl; ring C is an optionally substituted six-membered heterocycle containing at least one nitrogen atom and one to three double bond(s) in the ling wherein the atom at the point of attachment to ring B is a carbon atom; ring D is an optionally substituted five-membered ring containing one or two double bond(s) in the ring; A1 and A2 are independently nitrogen or carbon; m is 0 or 1; R represents H, —NHC(═O)RA, —NHC(═S)RA, —NH-het1, —O-het1, —S-het1, —S(═O)-het1, —S(═O)2-het1, het2, —CONHRA, —OH, lower alkyl, lower alkoxy or lower alkenyl; and het1 and het2 are independently a heterocyclic group; with the proviso that the fused ring C-D is not

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