573-54-6

Basic information

• Product Name: 2-Bromo-3-nitrobenzoic acid
• Synonyms: 2-BROMO-3-NITROBENZOIC ACID;TIMTEC-BB SBB003180;2-BROMO-3-NITROBENZOIC ACID, TECH., 90%;Benzoic acid, 2-bromo-3-nitro-;2-Bromo-3-nitrobenzoic acid 95%;2-BROMO-3-NITROBENAOIC ACID;2-BROMO-3-NITROBENZOIC ACID (KG LEVEL);2-Bromo-3-nitrobenzoic acid,95%
• CAS NO: 573-54-6
• Molecular Formula: C₇H₄BrNO₄
• Molecular Weight: 246.01
• EINECS: 209-356-3
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Carboxylic Acids;Phenyls & Phenyl-Het;Carboxylic Acids;Phenyls & Phenyl-Het;C7;Carbonyl Compounds
• Mol File: 573-54-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 184-186 °C(lit.)
• Boiling Point: 337.7 °C at 760 mmHg
• Flash Point: 158.1 °C
• Appearance: Off-white to yellow crystalline powder
• Density: 1.892 g/cm³
• Vapor Pressure: 4.02E-05mmHg at 25°C
• Refractive Index: 1.65
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Dichloromethane (Very Slightly), DMSO (Slightly)
• PKA: 1.85±0.20(Predicted)
• CAS DataBase Reference: 2-Bromo-3-nitrobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-3-nitrobenzoic acid(573-54-6)
• EPA Substance Registry System: 2-Bromo-3-nitrobenzoic acid(573-54-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• Hazardous Substances Data: 573-54-6(Hazardous Substances Data)

Usage

Chemical Properties

Off-white to yellow crystalline powder

Uses

2-Bromo-3-nitrobenzoic acid is used in preparation of 3-substituted 5-nitroisocoumarins1 and 2-bromo-3-nitrobenzaldehyde.

InChI:InChI=1/C7H4BrNO4/c8-6-4(7(10)11)2-1-3-5(6)9(12)13/h1-3H,(H,10,11)

Upstream product

• 603-11-2 3-nitrophthalic acid 
• 53663-14-2 anhydro-2-hydroxymercuri-3-nitrobenzoic acid 
• 88-65-3 2-bromobenzoic-acid 

Downstream Products

• 6286-36-8 2-bromo-3-nitrobenzoic acid chloride 
• 116529-60-3 2-bromo-3,5-dinitro-benzoic acid 
• 5337-09-7 2-bromo-3-nitro-benzoic acid methyl ester 
• 106987-79-5 N-(2-naphthyl)-3-nitroanthranilic acid 
• 102555-18-0 3,3'-dinitro-2,2'-p-phenylenediamino-di-benzoic acid 
• 24034-22-8 2-Brom-3-nitro-benzotrifluorid 
• 58718-49-3 2-<(2-carboxyphenyl)amino>-3-nitrobenzoic acid 
• 124154-64-9 2-methylseleno-3-nitrobenzoic acid 
• 106976-11-8 N-(2-chloro-6-fluorophenyl)-3-nitroanthranilic acid 
• 175347-01-0 2-Dimethylamino-3-nitrobenzoic acid 
• 369652-59-5 2-(1-methoxy-5-isoquinolineamino)-3-nitrobenzoic acid 
• 403712-66-3 2-(7-methoxy-naphthalen-1-ylamino)-3-nitrobenzoic acid 
• 879545-84-3 4-fluorophenyl 2-bromo-3-nitrobenzoate 
• 131514-79-9 2,3,4,5-tetrahydro-3-methyl-4-(phenylmethyl)-1H-1,4-benzodiazepin-9-amine 

Relevant articles and documents

INHIBITORS OF STEAROYL-COA DESATURASE

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.

Preparation and NMR analysis of 2,6-heterodifunctional halobenzenes as precursors for substituted biphenyls

Preparation and complete characterization of 16 2,6-disubstituted halobenzenes, including nine new compounds, from two common starting materials is described. Seven of the new compounds contain one or two propylthio groups, which have been introduced in two ways. Direct reaction of arenediazonium salts with 1-propanethiolate gives yields comparable to those obtained in a three-step method through sulfonyl chlorides. The 1H- and 13C NMR chemical shifts of 17 1,2,3-trisubstituted benzenes have been correlated with the predicted values and the observed trends explained using commonly available modeling packages.