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2-(2,6-dichlorophenyl)-4,5-dihydro-1,3-thiazole is a chemical compound with the molecular formula C8H7Cl2NS. It is a heterocyclic compound, specifically a thiazole derivative, which features a sulfur atom in the ring structure. 2-(2,6-dichlorophenyl)-4,5-dihydro-1,3-thiazole is characterized by the presence of two chlorine atoms attached to the phenyl ring at the 2nd and 6th positions, and the thiazole ring is fused to a dihydro structure, indicating the presence of two hydrogen atoms attached to the carbon atoms in the ring. It is an organic compound that may be used in various chemical and pharmaceutical applications due to its unique structure and properties.

3797-82-8

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3797-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3797-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3797-82:
(6*3)+(5*7)+(4*9)+(3*7)+(2*8)+(1*2)=128
128 % 10 = 8
So 3797-82-8 is a valid CAS Registry Number.

3797-82-8Downstream Products

3797-82-8Relevant academic research and scientific papers

A single-reagent-driven multistep one-pot preparation of thiazolines and 1,3-thiazines from aldoximes, nitriles, and carboxylic acids

Bhattacharyya, Shubhankar,Pathak, Uma

, p. 3553 - 3560 (2015/11/17)

N-(ω-Bromoalkyl)dichlorothiophosphoramidates have been designed as a new class of reagent for the single-reagent-driven multistep preparation of 2-substituted thiazolines and 1,3-thiazines from ald-oximes, nitriles, or carboxylic acids. A wide range of substrates both aromatic as well as aliphatic were investigated and found suitable for the developed protocol.

Easy access to thiazolines and thiazines via tandem S-alkylation- cyclodeamination of thioamides/haloamines

Pathak, Uma,Bhattacharyya, Shubhankar,Dhruwansh, Vishwanath,Pandey, Lokesh Kumar,Tank, Rekha,Suryanarayana, Malladi V. S.

supporting information; experimental part, p. 1648 - 1651 (2011/08/10)

This is the first report of a facile synthesis of thiazolines and thiazines from a self-catalyzed, water assisted tandem S-alkylation-cyclodeamination reaction of thioamides/haloamines. The reaction is clean and efficient with simple product work-up, and is applicable to a variety of substrates.

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