100959-22-6

Basic information

• Product Name: METHYL 2-BROMO-4-NITROBENZOATE
• Synonyms: METHYL 2-BROMO-4-NITROBENZOATE;2-BroMo-4-nitrobenzoic acid Methyl ester;3-Bromo-4-(methoxycarbonyl)nitrobenzene;4-nitro-2-broMobenzoic acid Methyl ester;Methyl 2-bromo-4-nitrobenzoate 97%;2-Bromo-4-nitro-benzoic acid methyleste
• CAS NO: 100959-22-6
• Molecular Formula: C₈H₆BrNO₄
• Molecular Weight: 260.04
• Product Categories: blocks;Bromides;Carboxes;NitroCompounds
• Mol File: 100959-22-6.mol
• Article Data: 24

Chemical Properties

• Melting Point: 82.0 to 86.0 °C
• Boiling Point: 339.199 °C at 760 mmHg
• Flash Point: 158.942 °C
• Appearance: /
• Density: 1.674 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.588
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 2-BROMO-4-NITROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-BROMO-4-NITROBENZOATE(100959-22-6)
• EPA Substance Registry System: METHYL 2-BROMO-4-NITROBENZOATE(100959-22-6)

Safety Data

• Hazardous Substances Data: 100959-22-6(Hazardous Substances Data)

Usage

General Description

Methyl 2-bromo-4-nitrobenzoate is a chemical compound with the molecular formula C8H6BrNO4. It is a yellow solid that is used in organic synthesis and chemical research. METHYL 2-BROMO-4-NITROBENZOATE is commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and dyes. It is also used as a building block for the synthesis of various other organic compounds. Methyl 2-bromo-4-nitrobenzoate is known for its strong nitro flavor and its potential as a reagent in organic reactions. It is important to handle this compound with care, as it is toxic and may cause skin and eye irritation upon contact.

InChI:InChI=1/C8H6BrNO4/c1-14-8(11)6-3-2-5(10(12)13)4-7(6)9/h2-4H,1H3

Upstream product

• 67-56-1 methanol 
• 16426-64-5 2-bromo-4-nitrobenzoic acid 
• 619-50-1 4-nitrobenzoic acid methyl ester 
• 7745-93-9 2-bromo-4-nitrotoluene 
• 856794-72-4 2-bromo-4-nitrobenzoyl chloride 
• 74-88-4 methyl iodide 
• 3558-19-8 methyl 2-amino-4-nitrobenzoate 
• 186581-53-3 diazomethane 

Downstream Products

• 959778-15-5 methyl 4-nitro-2-vinyl-benzoate 
• 959778-16-6 4-nitro-2-vinylbenzoic acid ethyl ester 
• 1344109-47-2 2-bromo-4-(pyrrol-1-yl)benzyl alcohol 
• 1344109-66-5 phenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-2-yl)methanone 
• 1344109-55-2 phenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-3-yl)methanone 
• 1344109-58-5 4-fluorophenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-3-yl)methanone 
• 1344109-67-6 4-fluorophenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-2-yl)methanone 
• 1344109-70-1 2-chlorophenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-2-yl)methanone 
• 1344109-59-6 C₁₈H₁₃BClNO₃ 
• 1572936-67-4 2-(4-methoxynaphthalen-1-ylamino)-4-nitrobenzoic acid 
• 90656-48-7 N-(4-chlorophenyl)-4-nitroanthranilic acid 
• 26690-13-1 N-(4-bromophenyl)-4-nitroanthranilic acid 
• 1578179-09-5 N-(4-trifluoromethylphenyl)-4-nitroanthranilic acid 
• 20983-73-7 N-(4-nitrophenyl)-4-nitroanthranilic acid 

Relevant articles and documents

Synthesis of a coronene analogue containing an amide bond by Pd-mediated intramolecular C[sbnd]C bond formation of 2-halogenated 4-(alkylamino)benzoic acid cyclic trimer

A coronene analogue containing amide linkage was synthesized from a halogenated cyclic triamide by palladium-mediated intramolecular C[sbnd]C bond formation. The cyclic triamide was formed from the condensation of 2-chloro-4-(isobutylamino)benzoic acid in

An Activatable Lanthanide Luminescent Probe for Time-Gated Detection of Nitroreductase in Live Bacteria

Herein we report the development of a turn-on lanthanide luminescent probe for time-gated detection of nitroreductases (NTRs) in live bacteria. The probe is activated through NTR-induced formation of the sensitizing carbostyril antenna and resulting energ

Explicit treatment of active-site waters enhances quantum mechanical/implicit solvent scoring: Inhibition of CDK2 by new pyrazolo[1,5-a]pyrimidines

We present comprehensive testing of solvent representation in quantum mechanics (QM)-based scoring of protein-ligand affinities. To this aim, we prepared 21 new inhibitors of cyclin-dependent kinase 2 (CDK2) with the pyrazolo[1,5-a]pyrimidine core, whose