29048-34-8

Basic information

• Product Name: 5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID
• Synonyms: AKOS BB-8341;5-(2-NITRO-PHENYL)-FURAN-2-CARBOXYLIC ACID;5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID;5-(2-NITROPHENYL)-2-FUROIC ACID;ASISCHEM T31189;ART-CHEM-BB B025356;LABOTEST-BB LT00159379;TIMTEC-BB SBB003260
• CAS NO: 29048-34-8
• Molecular Formula: C₁₁H₇NO₅
• Molecular Weight: 233.18
• Mol File: 29048-34-8.mol
• Article Data: 18

Chemical Properties

• Melting Point: 216-219 °C(lit.)
• Boiling Point: 433.4°C at 760mmHg
• Flash Point: 215.9°C
• Appearance: /
• Density: 1.44g/cm³
• Vapor Pressure: 2.79E-08mmHg at 25°C
• CAS DataBase Reference: 5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID(29048-34-8)
• EPA Substance Registry System: 5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID(29048-34-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 29048-34-8(Hazardous Substances Data)

Usage

General Description

5-(2-Nitrophenyl)-2-furancarboxylic acid is a chemical compound with the molecular formula C12H7NO5. It belongs to the class of organic compounds known as nitrobenzenes. 5-(2-NITROPHENYL)-2-FURANCARBOXYLIC ACID is a derivative of furan and contains a nitrophenyl group. It is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. The presence of the nitro group makes this compound a potential mutagen and a known skin irritant, and it should be handled and used with caution. Overall, 5-(2-nitrophenyl)-2-furancarboxylic acid is a versatile compound that has various industrial applications but requires careful handling due to its potential hazards.

InChI:InChI=1/C11H7NO5/c13-11(14)10-6-5-9(17-10)7-3-1-2-4-8(7)12(15)16/h1-6H,(H,13,14)/p-1

Upstream product

• 88-14-2 2-furanoic acid 
• 88-74-4 2-nitro-aniline 
• 98-01-1 furfural 
• 2527-99-3 methyl 5-bromo-2-furoate 
• 5570-19-4 2-nitrophenylboronic acid 
• 41019-36-7 5-(2-nitrophenyl)furan-2-carboxylic acid methyl ester 

Downstream Products

• 1026577-55-8 C₁₇H₁₁NO₇S 
• 453557-59-0 2-(5-(2-nitrophenyl)-2-furoylamido)-5-(4-methoxyphenyloxymethyl)-1,3,4-thiadiazole 
• 1255501-31-5 N-(4-ethoxybenzoyl)-N′-[5-(2′-nitrophenyl)-2-furoyl]hydrazine 
• 1255501-30-4 N-(4-methoxybenzoyl)-N′-[5-(2′-nitrophenyl)-2-furoyl]hydrazine 
• 1255501-28-0 N-(4-chlorobenzoyl)-N′-[5-(2′-nitrophenyl)-2-furoyl]hydrazine 
• 1255501-32-6 N-(4-bromobenzoyl)-N'-[5-(2-nitrophenyl)-2-furoyl]hydrazine 
• 1255501-29-1 N-(2-chlorobenzoyl)-N'-[5-(2-nitrophenyl)-2-furoyl]hydrazine 
• 20000-96-8 5-(2-nitrophenyl)-2-furaldehyde 
• 1428422-58-5 2-chloro-5-{5-[5-(2-nitro-phenyl)-furan-2-ylmethylene]-4-oxo-thiazolidin-2-ylideneamino}-benzoic acid 

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

Novel S-Thiazol-2-yl-furan-2-carbothioate Derivatives as Potential T3SS Inhibitors against Xanthomonas oryzae on Rice

Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv oryzae (Xoo) is considered as the most destructive disease of rice. The use of bactericides is among the most widely used traditional methods to control this destructive disease. The excessive an