96232-71-2

Basic information

• Product Name: METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE
• Synonyms: METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE;4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
• CAS NO: 96232-71-2
• Molecular Formula: C₆H₄Br₂O₃S
• Molecular Weight: 315.97
• Mol File: 96232-71-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 125-128°C
• Boiling Point: 321.6°Cat760mmHg
• Flash Point: 148.3°C
• Appearance: /
• Density: 2.394g/cm³
• Vapor Pressure: 0.00113mmHg at 25°C
• Refractive Index: 1.647
• PKA: 6.97±0.20(Predicted)
• CAS DataBase Reference: METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE(96232-71-2)
• EPA Substance Registry System: METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE(96232-71-2)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 96232-71-2(Hazardous Substances Data)

Usage

General Description

METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE is a chemical compound that belongs to the thiophene family. It is a derivative of thiophene, a five-membered heterocyclic compound containing a sulfur atom. The presence of two bromine atoms and a carboxylate group in the chemical structure gives it unique properties and potential applications in organic synthesis, pharmaceuticals, and agrochemicals. METHYL 4,5-DIBROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE is commonly used as an intermediate in the production of various functional materials, including pharmaceutical ingredients and agrochemicals. It also has potential applications in the field of organic electronics due to its electronic properties. Additionally, its structure and properties make it useful in the development of new chemical compounds and materials.

InChI:InChI=1/C6H4Br2O3S/c1-11-6(10)4-3(9)2(7)5(8)12-4/h9H,1H3

Upstream product

• 5118-06-9 methyl 3-hydroxy-2-thiophenecarboxylate 

Downstream Products

• 1047644-95-0 N-[2-amino-1-(phenylmethyl)ethyl]-4-bromo-3-(methyloxy)-5-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxamide hydrochloride 
• 1047644-93-8 1,1-dimethylethyl [2-({[4-bromo-3-(methyloxy)-5-(1-methyl-1H-pyrazol-5-yl)-2-thienyl]carbonyl}amino)-3-phenylpropyl]carbamate 
• 1047643-75-3 N-[2-amino-1-(phenylmethyl)ethyl]-4-bromo-3-(methyloxy)-5-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxamide 
• 1246405-92-4 methyl 5-(2-chlorophenyl)-4-(4-chlorophenyl)-3-hydroxy-thiophene-2-carboxylate 
• 1246405-84-4 methyl 4-bromo-5-(2-chlorophenyl)-3-methoxythiophene-2-carboxylate 
• 1246405-81-1 methyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-3-methoxythiophene-2-carboxylate 
• 1246405-82-2 methyl 4-bromo-5-(2,4-dichlorophenyl)-3-methoxythiophene-2-carboxylate 
• 1246405-94-6 5-(2-Chlorophenyl)-4-(4-chlorophenyl)-3-[3-(tetrahydro-2H-pyran-2-yloxy)propoxy]thiophene-2-carboxylic acid 
• 1246405-93-5 Methyl 5-(2-chlorophenyl)-4-(4-chlorophenyl)-3-[3-(tetrahydro-2H-pyran-2-yloxy)propoxy]thiophene-2-carboxylate 
• 1246405-85-5 4-(4-Chlorophenyl)-5-(2,4-dichlorophenyl)-3-methoxythiophene-2-carboxylic acid 
• 1246405-83-3 Methyl 5-(2-chlorophenyl)-4-(4-chlorophenyl)-3-methoxy-thiophene-2-carboxylate 
• 175137-42-5 Methyl 4,5-dibromo-3-methoxythiophene-2-carboxylate 
• 1346685-15-1 C₂₀H₂₀O₄S 
• 1346685-11-7 2,5-bis(hydroxymethyl)-4-[4-(methyloxy)phenyl]-3-thienyl trifluoromethanesulfonate 

Relevant articles and documents

N-1H-Tetrazol-5-yl-(5-Ring)-carboxamide-derivatives, a process for their manufacture, and the use thereof

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N-1H-tetrazol-5-yl-2-thiophene carboxamides, N-1H-tetrazol-5-yl-2-pyrrole carboxamides, N-1H-tetrazol-5-yl-2-furan carboxamides, and anti-allergic and anti-inflammatory use thereof

The present invention is for compounds having the formula of N-1H-tetrazol-5-yl-2-thiophenecarboxamides, N-1H-tetrazol-5-yl-2-pyrrolecarboxamides, N-1H-tetrazol-5-yl-2-furancarboxamides or analogs of each of the carboxamides. The compounds are useful for the treatment of allergic or inflammatory conditions or diseases. Thus, pharmaceutical compositions and methods of use are also the invention. Processes of preparation for the compounds are also the invention.