35757-20-1

Basic information

• Product Name: 2-Bromo-3-nitroaniline
• Synonyms: 2-Bromo-3-nitroaniline
• CAS NO: 35757-20-1
• Molecular Formula: C₆H₅BrN₂O₂
• Molecular Weight: 217.03
• Mol File: 35757-20-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 2-Bromo-3-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-3-nitroaniline(35757-20-1)
• EPA Substance Registry System: 2-Bromo-3-nitroaniline(35757-20-1)

Safety Data

• Hazardous Substances Data: 35757-20-1(Hazardous Substances Data)

Usage

General Description

2-Bromo-3-nitroaniline is a chemical compound with the molecular formula C6H5BrN2O2. It is a pale yellow solid that is primarily used in the synthesis of various organic compounds. It is commonly utilized as an intermediate in the production of pharmaceuticals, dyes, and agrochemicals. The compound is an important building block in organic chemistry and is often used in the manufacture of various products. Due to its chemical properties, 2-Bromo-3-nitroaniline is considered to be a hazardous substance and should be handled with care and in accordance with proper safety protocols.

Upstream product

• 35757-19-8 2-bromo-3-nitrobenzamide 
• 19128-47-3 N_.N-Diacetyl-2-brom-3-nitro-anilin 
• 99-09-2 3-nitro-aniline 
• 606-22-4 2,6-dinitroaniline 
• 573-54-6 2-bromo-3-nitro-benzoic acid 
• 603-11-2 3-nitrophthalic acid 
• 19128-46-2 2-Brom-3-nitro-benzoylazid 
• 6286-36-8 2-bromo-3-nitrobenzoic acid chloride 
• 4185-79-9 2-bromo-1,3-dinitrobenzene 

Downstream Products

• 116670-83-8 (2-bromo-3-nitro-phenyl)-phosphonic acid 
• 32337-95-4 2-bromo-1-iodo-3-nitrobenzene 
• 642068-70-0 1-bromo-2-nitro-6-propylthiobenzene 
• 1260764-95-1 tert-butyl 2-bromo-3-nitrophenylcarbamate 

Relevant articles and documents

Preparation method of 2 -bromo -3 -fluoronitrobenzene

The preparation method of 2 -bromo -3 -fluoronitrobenzene comprises the following steps: (1) reacting m-nitroaniline with bromosuccinimide to generate a compound III. (2) Compound III reacts with sodium nitrite and fluoroboric acid to generate compound IV

Electrophilic bromination of meta-substituted anilines with N-bromosuccinimide: Regioselectivity and solvent effect

N-Bromosuccinimide-mediated electrophilic aromatic bromination of a series of anilines substituted with an electron-with-drawing group in the meta position was investigated. The regioselectivity of the reaction is markedly dependent on the polarity of the solvent and the bromination reaction can be tuned by appropriate selection of the reaction medium. Georg Thieme Verlag Stuttgart.

BISHYDROGEN DIBROMOBROMATE - A NEW BROMINATING AGENT

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