10546-63-1

Basic information

• Product Name: 2,6-Dibromo-4-ethylaniline
• Synonyms: 2,6-Dibromo-4-ethylaniline
• CAS NO: 10546-63-1
• Molecular Formula: C₈H₉Br₂N
• Molecular Weight: 278.97176
• Mol File: 10546-63-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-Dibromo-4-ethylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dibromo-4-ethylaniline(10546-63-1)
• EPA Substance Registry System: 2,6-Dibromo-4-ethylaniline(10546-63-1)

Safety Data

• Hazardous Substances Data: 10546-63-1(Hazardous Substances Data)

Usage

Classification

Organic compound

Derivative

Aniline

Bromine atoms

Present at the 2 and 6 positions on the benzene ring

Ethyl group

Attached to the amino group on the 4 position

Common use

Intermediate in the synthesis of various organic compounds and pharmaceuticals

Potential applications

Medicinal chemistry and drug development

Reactivity

Versatile

Handling precautions

May pose health hazards and environmental risks if not properly managed

Upstream product

• 589-16-2 4-aminoethylbenzene 
• 59626-77-6 4-ethylanilinium hydrochloride 
• 7732-18-5 water 
• 7726-95-6 bromine 

Relevant articles and documents

Method of catalytically synthesizing polybromo-aniline in water phase

The invention discloses a method of catalytically synthesizing polybromo-aniline in a water phase. The method comprises following steps: adding a catalytic amount of a free radical initiator, aniline derivatives, cheap and low-toxic bromine salts, and water into a reactor; carrying out reactions in a photocatalytic reaction instrument under power of 5W at a room temperature; after a while, extracting the reaction product by ethyl acetate, and carrying out recrystallization to obtain polybromo-aniline; wherein the free radical initiator is eosin, sodium persulfate, or potassium persulfate. The power of the incandescent lamp of the photocatalytic reaction instrument is 5W. The free radical initiator and bromine salts are cheap and easily available. The method is an ideal synthesis method of polybromo-aniline. Cheap and low-toxic bromine salts are used to replace liquid bromine. The cheap and easily available free radical initiator is used to replace unstable and explosive hydrogen peroxide. After 4 to 10 hours of reactions under the power of 5W, polybromo-aniline can be synthesized, the yield and the reaction selectivity are high, the byproducts are few, and the post treatment is simple.