16582-78-8

Basic information

• Product Name: 3-Bromo-4-thiocyanatoaniline
• Synonyms: 3-Bromo-4-thiocyanatoaniline;4-Amino-2-bromophenylthiocyanate;Thiocyanic acid, 4-amino-2-bromophenyl ester
• CAS NO: 16582-78-8
• Molecular Formula: C₇H₅BrN₂S
• Molecular Weight: 229.097
• Mol File: 16582-78-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Bromo-4-thiocyanatoaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-4-thiocyanatoaniline(16582-78-8)
• EPA Substance Registry System: 3-Bromo-4-thiocyanatoaniline(16582-78-8)

Safety Data

• Hazardous Substances Data: 16582-78-8(Hazardous Substances Data)

Usage

General Description

3-Bromo-4-thiocyanatoaniline is a chemical compound with the molecular formula C7H5BrN2S. It is a derivative of aniline and is characterized by the presence of a bromine atom and a thiocyanate group attached to the aromatic ring. 3-Bromo-4-thiocyanatoaniline has various applications in organic synthesis and pharmaceutical research, particularly in the development of new drugs. It is known for its potential use in the synthesis of biologically active molecules and is a valuable building block in the pharmaceutical industry. Additionally, 3-Bromo-4-thiocyanatoaniline is used in the production of dyes and pigments, and is an important intermediate in the synthesis of various organic compounds. Due to its versatility and potential applications, this chemical compound is of interest to researchers in the fields of chemistry, medicine, and materials science.

Upstream product

• 591-19-5 m-Bromoaniline 
• 333-20-0 potassium thioacyanate 
• 1147550-11-5 ammonium thiocyanate 

Relevant articles and documents

Method for inducing thiocyanation of arylamine compound by visible light

The invention discloses a method for inducing thiocyanation of an arylamine compound by visible light. Specifically, in the atmosphere of oxygen or air, an arylamine compound, an ammonium thiocyanatecompound and copper chloride dihydrate are added into a

Copper-Catalyzed Aerobic Oxidative Regioselective Thiocyanation of Aromatics and Heteroaromatics

A copper-catalyzed aerobic oxidative reaction between aromatics or heteroaromatics with KSCN is developed by using O2 as the oxidant. The combination of Cu(OTf)2, N,N,N′,N′-tetramethylethylenediamine (TMEDA) and BF3·Et2O provides an efficient catalytic system, affording substituted thiocyanation products and 2-aminobenzothiazoles in excellent yields. The reaction also possesses a good functional group tolerance for both strong electron-withdrawing and electron-donating groups.

Heterogeneous and catalytic thiocyanation of aromatic compounds in aqueous media

This article describes a highly efficient heterogeneous catalytic thiocyanation of indoles, substituted anilines (electron rich and electron deficient) and N-substituted aromatic amines in water under mild and green conditions. The reaction of substrates