208665-96-7

Basic information

• Product Name: 3-Bromo-4-isobutoxybenzothioamide
• Synonyms: 3-Bromo-4-isobutoxybenzothioamide;3-broMo-4-(2-Methylpropoxy)benzene-1-carbothioaMide;3-bromo-4-isobutoxy-benzenecarbothioamide;3-bromo-4-isobutoxyphenylthiocarboxamide
• CAS NO: 208665-96-7
• Molecular Formula: C₁₁H₁₄BrNOS
• Molecular Weight: 288.208
• Product Categories: Pharmaceutical Intermediates
• Mol File: 208665-96-7.mol

Chemical Properties

• Boiling Point: 370.783 °C at 760 mmHg
• Flash Point: 178.043 °C
• Appearance: /
• Density: 1.398 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 3-Bromo-4-isobutoxybenzothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-4-isobutoxybenzothioamide(208665-96-7)
• EPA Substance Registry System: 3-Bromo-4-isobutoxybenzothioamide(208665-96-7)

Safety Data

• Hazardous Substances Data: 208665-96-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
3-Bromo-4-isobutoxybenzothioamide is utilized as a research compound for its potential anti-inflammatory and analgesic properties. It is employed in scientific studies to explore its pharmacological effects and possible therapeutic applications, with the aim of understanding its impact on inflammatory and painful conditions.
Used in Enzyme and Receptor Modulation Studies:
In the field of biochemistry, 3-Bromo-4-isobutoxybenzothioamide is used as a tool to investigate its interaction with enzymes and receptors. This helps researchers to uncover its mechanism of action and assess its potential as a lead compound for the development of new pharmaceutical drugs.
Used in Drug Development:
3-Bromo-4-isobutoxybenzothioamide is considered in the drug development process as a candidate for further research. Its pharmacological profile is being studied to determine its full potential, with ongoing research aimed at understanding its efficacy and safety for use in treating specific conditions.

InChI:InChI=1/C11H14BrNOS/c1-7(2)6-14-10-4-3-8(11(13)15)5-9(10)12/h3-5,7H,6H2,1-2H3,(H2,13,15)

Upstream product

• 208665-95-6 3-bromo-4-isobutoxybenzonitrile 
• 767-00-0 4-cyanophenol 
• 2315-86-8 3-bromo-4-hydroxybenzonitrile 

Downstream Products

• 144060-96-8 2-(3-bromo-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylic acid ethyl ester 

Relevant articles and documents

2 - (3-cyano-4-alkoxy) phenyl-4-substituted thiazole-5- formic acid class compound, composition and its preparation and use

The invention relates to a 2-(3-cyano-4-alkoxy) phenyl-4-substituted thiazole-5-formic acid compound which has xanthine oxidase inhibitory activity and is shown in a general formula I, a composition and preparation methods thereof. The invention also relates to applications of the compound and the composition thereof to preparation of medicaments for treating and/or preventing hyperuricemia and gout diseases. In the formula I, R2 is substituted or unsubstituted phenyl or a substituted or unsubstituted heteroaromatic radical, R1 is a substitutive aliphatic group of a straight chain or a branched chain, substituted or unsubstituted alicyclic hydrocarbonyl or substituted or unsubstituted aryl alkyl and A is an oxygen atom, a sulfur atom or a nitrogen atom.

A PROCESS FOR THE PREPARATION OF FEBUXOSTAT

The present invention relates to a process for the preparation of Febuxostat, useful in the pharmaceutical field for the treatment of the hyperuricemia.