52938-96-2

Basic information

• Product Name: 5-(4-BROMOPHENYL)-2-FUROIC ACID 98
• Synonyms: 5-(4-BROMOPHENYL)-2-FUROIC ACID 98;5-(2,4-Dimethoxyphenyl)-furan-2-carboxylic acid;5-(3,4-Dimethoxyphenyl)-furan-2-carboxylic acid;5-(3,5-Dimethoxyphenyl)-furan-2-carboxylic acid;5-(4-Bromopheneyl)-2-furancarboxylic acid;5-(Benzo[1,3]dioxol-5-yl)-furan-2-carboxylic acid;5-(4-bromophenyl)-2-furancarboxylic acid
• CAS NO: 52938-96-2
• Molecular Formula: C₁₁H₇BrO₃
• Molecular Weight: 267.08
• Product Categories: Building Blocks;Furans;FuransHeterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Building Blocks;C8 to C11;C9 to C11;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks
• Mol File: 52938-96-2.mol
• Article Data: 15

Chemical Properties

• Melting Point: 205-209 °C(lit.)
• Boiling Point: 415.1°C at 760 mmHg
• Flash Point: 204.9°C
• Appearance: /
• Density: 1.606g/cm³
• Vapor Pressure: 1.23E-07mmHg at 25°C
• Refractive Index: 1.611
• PKA: 3.00±0.10(Predicted)
• CAS DataBase Reference: 5-(4-BROMOPHENYL)-2-FUROIC ACID 98(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-BROMOPHENYL)-2-FUROIC ACID 98(52938-96-2)
• EPA Substance Registry System: 5-(4-BROMOPHENYL)-2-FUROIC ACID 98(52938-96-2)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 52938-96-2(Hazardous Substances Data)

Usage

Appearance

white to off-white crystalline powder

Purity

98%

Usage

building block for synthesis of organic compounds in pharmaceutical and chemical industries

Structure

furoic acid core with bromophenyl substituent
Versatile compound for designing and developing new drugs, agrochemicals, and specialty chemicals
Potential applications in research and development as a reagent or intermediate for production of new materials or compounds

InChI:InChI=1/C11H7BrO3/c12-8-3-1-7(2-4-8)9-5-6-10(15-9)11(13)14/h1-6H,(H,13,14)

Upstream product

• 88-14-2 2-furanoic acid 
• 106-40-1 4-bromo-aniline 
• 52939-02-3 methyl 5-(4-bromophenyl)furan-2-carboxylate 
• 98-01-1 furfural 
• 20005-42-9 5-(4-bromophenyl)-2-furancarboxyaldehyde 

Downstream Products

• 60335-98-0 5-(4-bromo-phenyl)-furan-2-carbonyl chloride 
• 139268-12-5 6-<5-(4-Bromophenyl)-2-furyl>-3-p-chlorophenyl-1,2,4-triazolo<3,4-b>-1,3,4-thiadiazole 
• 139268-07-8 6-<5-(4-Bromophenyl)-2-furyl>-3-methyl-1,2,4-triazolo<3,4-b>-1,3,4-thiadiazole 
• 139268-08-9 6-<5-(4-Bromophenyl)-2-furyl>-3-ethyl-1,2,4-triazolo<3,4-b>-1,3,4-thiadiazole 
• 139268-09-0 6-<5-(4-Bromophenyl)-2-furyl>-3-propyl-1,2,4-triazolo<3,4-b>-1,3,4-thiadiazole 
• 139268-10-3 6-<5-(4-Bromophenyl)-2-furyl>-3-phenyl-1,2,4-triazolo<3,4-b>-1,3,4-thiadiazole 
• 92972-97-9 {[1-[5-(4-Bromo-phenyl)-furan-2-yl]-1-chloro-meth-(Z)-ylidene]-amino}-acetic acid ethyl ester 
• 92973-18-7 {[5-(4-Bromo-phenyl)-furan-2-carbonyl]-amino}-acetic acid ethyl ester 
• 93770-55-9 {5-[5-(4-Bromo-phenyl)-furan-2-yl]-tetrazol-1-yl}-acetic acid 
• 92973-08-5 {5-[5-(4-Bromo-phenyl)-furan-2-yl]-tetrazol-1-yl}-acetic acid ethyl ester 
• 1004111-80-1 5-(4-(5-formylfuran-2-yl)phenyl)furan-2-carboxylic acid 
• 1255501-40-6 N-(4-ethoxybenzoyl)-N'-[5-(4-bromophenyl)-2-furoyl]hydrazine 
• 1255501-39-3 N-(4-methoxybenzoyl)-N'-[5-(4-bromophenyl)-2-furoyl]hydrazine 
• 637306-79-7 N-(4-chlorobenzoyl)-N'-[5-(4-bromophenyl)-2-furoyl]hydrazine 

Relevant articles and documents

Discovery of a series of 5-phenyl-2-furan derivatives containing 1,3-thiazole moiety as potent Escherichia coli β-glucuronidase inhibitors

Gut microbial β-glucuronidases have drawn much attention due to their role as a potential therapeutic target to alleviate some drugs or their metabolites-induced gastrointestinal toxicity. In this study, fifteen 5-phenyl-2-furan derivatives containing 1,3

Thiazolidin-2-cyanamides derivatives as novel potent Escherichia coli β-glucuronidase inhibitors and their structure–inhibitory activity relationships

Gut microbial β-glucuronidases have the ability to deconjugate glucuronides of some drugs, thus have been considered as an important drug target to alleviate the drug metabolites-induced gastrointestinal toxicity. In this study, thiazolidin-2-cyanamide de

2-furoylamide compound and preparation and application thereof

The invention discloses a 2-furancarboxamide compound and a preparation method and application thereof. The 2-furancarboxamide compound is obtained by reacting a compound as shown in a formula II with9H-pyridino[3,4-b]indole in the presence of an acid-bin