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2,3,5,6-tetrabromoaniline is a chemical compound that belongs to the class of anilines, which are aromatic amines derived from benzene. It is a derivative of aniline, with four bromine atoms attached to the benzene ring at the 2, 3, 5, and 6 positions. 2,3,5,6-tetrabromoaniline is known for its strong nucleophilic and electrophilic properties, making it a useful reagent in organic chemistry reactions.

84483-23-8

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84483-23-8 Usage

Uses

Used in Industrial Applications:
2,3,5,6-tetrabromoaniline is used as a chemical intermediate for the synthesis of dyes, pharmaceuticals, and agrochemicals. Its unique structure and reactivity contribute to the development of various products in these industries.
Used in Laboratory Research:
2,3,5,6-tetrabromoaniline is used as a reagent in organic chemistry reactions, facilitating the study of chemical properties and reaction mechanisms. Its strong nucleophilic and electrophilic properties make it a valuable tool for researchers in the field.
Used in Pharmaceutical Synthesis:
2,3,5,6-tetrabromoaniline is used as a building block in the synthesis of certain pharmaceutical compounds. Its reactivity allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Production:
2,3,5,6-tetrabromoaniline is used as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the development of effective products for agricultural use.
Safety Precautions:

Check Digit Verification of cas no

The CAS Registry Mumber 84483-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84483-23:
(7*8)+(6*4)+(5*4)+(4*8)+(3*3)+(2*2)+(1*3)=148
148 % 10 = 8
So 84483-23-8 is a valid CAS Registry Number.

84483-23-8Downstream Products

84483-23-8Relevant academic research and scientific papers

Regioselectivity of reductive debromination of substituted pentabromobenzenes with sodium tert-butoxide in DMSO

Shishkin,Tarasova,Butin

, p. 2379 - 2383 (2007/10/03)

The regioselectivity of reductive debromination of substituted pentabromobenzenes C6Br5X (X = NH2, OMe, Me, H, Cl, F, and NO2) under the action of ButONa in DMSO containing ButOH has been studied. The reaction followed the halophilic mechanism via carbanions.

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