229643-15-6

Usage

Chemical structure

Contains a benzothiazole ring with an iodomethyl substituent attached to it.

Usage

Mainly used as a building block in the synthesis of various organic compounds.

Industries

Particularly used in the pharmaceutical and agrochemical industries.

Reactivity

Known for its reactivity and ability to participate in a wide range of chemical reactions.

Molecular structure

Useful for the creation of diverse molecular structures.

Handling precautions

Important to handle with care, as iodine-containing compounds can be toxic and may pose environmental hazards if not handled properly.

InChI:InChI=1/C8H6INS/c9-5-8-10-6-3-1-2-4-7(6)11-8/h1-4H,5H2

Upstream product

• 120-75-2 2-Methylbenzothiazole 
• 37859-43-1 2-chloromethylbenzothiazole 
• 37859-42-0 1,3-benzothiazol-2-ylmethanol 

Downstream Products

• 120-75-2 2-Methylbenzothiazole 
• 6639-57-2 benzothiazole-2-carbaldehyde 
• 37859-42-0 1,3-benzothiazol-2-ylmethanol 
• 107401-57-0 1-(benzo[d]thiazol-2-yl)-3-methylbutan-2-ol 

Relevant academic research and scientific papers

Synthesis of New P-substituted Iminophosphoranes Via Staudinger Raction and Antimicrobial Activity Evaluation

A class of two series of new P-substituted iminophosphoranes, N-(1,3-benzothiazol-2-ylmethyl)-N-(alkyl subtituted-λ5-phosphanylidene)amine 5(a-e) and N-(alkyl substituted-λ5-phosphanylidene)-(3,5-difluorophenyl)methanamine 9(a-e) was

Copper(II) catalyzed heterobenzylic C(sp3)-H activation: Two efficient halogenation methodologies towards heterobenzyl halides

Two practical and simple synthetic methodologies towards various heterobenzyl halides were developed. A series of 2-halomethylquinolines were readily prepared by the one-pot reaction of 2-methylquinolines with CuX (X = I, Br, Cl) and TBHP in CH3CN. A large variety of heterobenzyl iodides, including 2-iodomethylquinolines, 2-iodomethylquinoxalines, 2-iodiomethylbenzooxazole, and 2-iodiomethylbenzothiazole, were efficiently synthesized by one-pot reaction of 2-methylheterocycles with iodine in the presence of CuSO4·5H2O in CH3CN.

Catalytic Aerobic Photo-oxidation of a Methyl Group on a Heterocycle to Produce an Aldehyde via Homolytic C-I Bond Cleavage caused by Irradiation with Visible Light

A new catalytic method was developed for photo-oxidizing the methyl group on aromatic heterocycles such as benzothiazole, benzoxazole, and quinoline to produce the corresponding aldehyde. This is the first report of the metal-free catalytic synthesis of benzothiazole-2-carboxaldehydes using molecular oxygen as the terminal oxidant.

PIPERIDINONES USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, m and n have meanings given in the description, and pharmaceutically acceptable derivatives thereof, which compounds are useful in the treatment of diseases and conditions associated with inflammation.

Samarium Barbier reactions of α-iodomethyloxazoles and thiazoles with aliphatic aldehydes

(Chemical Equation Presented) The reductive coupling of substituted α-iodomethyloxazoles and thiazoles with aliphatic aldehydes under Barbier conditions provides an effective method for the direct incorporation of intact heterocyclic systems.