13616-71-2

Basic information

• Product Name: 2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl-
• CAS NO: 13616-71-2
• Molecular Formula: C12H14BrNS
• Molecular Weight: 284.22
• Mol File: 13616-71-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl-(13616-71-2)
• EPA Substance Registry System: 2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl-(13616-71-2)

Safety Data

• Hazardous Substances Data: 13616-71-2(Hazardous Substances Data)

Usage

General Description

2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl- is a chemical compound that belongs to the class of 2H-1,2-thiazines. It is a heterocyclic compound that contains a thiazine ring system with a bromophenyl group attached to it. 2H-1,2-Thiazine, 2-(4-bromophenyl)-3,6-dihydro-4,5-dimethyl- is also known by its Chemical Abstracts Service (CAS) number 109393-40-1. It has the molecular formula C11H12BrNOS and a molecular weight of 285.19 g/mol. The compound is used in the field of pharmaceuticals and organic synthesis, and it has potential applications in medicinal chemistry for developing new drugs and pharmaceutical products.

Upstream product

• 13616-64-3 N,N'-thiodi(p-bromoaniline) 
• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 60731-73-9 2,6-difluorobenzoyl isocyanate 
• 118622-96-1 N-(4-bromophenylaminothio)phthalimide 
• 157736-04-4 C₉H₁₃BrClNSSi 
• 182260-22-6 C₆H₅BrClNS 
• 106-40-1 4-bromo-aniline 

Relevant articles and documents

Metal-assisted fragmentation of N-aryl- and -alkyl-N-trimethylsilylaminosulfur chlorides and N-aryl- and -alkyl-aminosulfur chlorides in the presence of conjugated dienes: Synthesis and reactivity of 2-substituted-3,6-dihydro-1,2-thiazines

N-Alkyl- and -aryl-N-trimethylsilylaminosulfur chlorides 2 and N-aryl- and -alkyl-aminosulfur chlorides 8 fragment in the presence of silver ions and a conjugated diene to yield 2-substituted-3,6-dihydro-1,2-thiarines 6 as the major products, possibly via

Diels-Alder and Ene Reactions of New Transient Thionitrosoarenes (Ar-N=S) and Thionitrosoheteroarenes (Het-N=S) Generated from N-(Arylaminosulfanyl)- and N-(Heteroarylaminosulfanyl)-phthalimides: Synthesis of Cyclic and Acyclic Sulfenamides

A series of new N-(arylaminosulfanyl)- and N-(heteroarylaminosulfanyl)-phthalimide derivatives 3i-m and 3o-r, has been prepared by reaction of chlorosulfanylphthalimide with the trimethylsilyl derivative of the appropriate arylamine or heteroarylamine.On

Efficient Generation of Thionitrosoarenes (ArN=S) by Fragmentation of N-(Arylaminothio)phthalimides

Base-induced fragmentation of a series of N-(arylaminothio)phyhalimides (3) provides an efficient route to transient thionitrosoarenes (2); compounds (2) have been trapped as Diels-Alder cycloadducts with butadiene and 2,3-dimethylbutadiene, or as ene add