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4-cyanobenzyl dimethylcarbamodithioate is a chemical compound with the molecular formula C10H10N2S2. It is an organic compound that features a 4-cyanobenzyl group attached to a dimethylcarbamodithioate moiety. 4-cyanobenzyl dimethylcarbamodithioate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the preparation of certain pesticides and other chemical intermediates. Its structure includes a cyano group (-CN) attached to a benzene ring, which is connected to a dithiocarbamate group, characterized by the presence of two sulfur atoms bonded to a central carbon atom. The compound's properties, such as its reactivity and stability, make it a valuable component in the development of new chemical entities.

834-23-1

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834-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 834-23-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 834-23:
(5*8)+(4*3)+(3*4)+(2*2)+(1*3)=71
71 % 10 = 1
So 834-23-1 is a valid CAS Registry Number.

834-23-1Downstream Products

834-23-1Relevant academic research and scientific papers

Transition-Metal-Free C(sp3)–S Coupling in Water: Synthesis of Benzyl Dithiocarbamates Using Thiuram Disulfides as an Organosulfur Source

Peng, Han-Ying,Dong, Zhi-Bing

, p. 949 - 956 (2018/11/27)

A simple, highly efficient and environmentally benign method for the synthesis of benzyl dithiocarbamates was reported. Without addition of metal catalyst, a series of 34 benzyl dithiocarbamates were obtained in good to excellent yields by treating benzyl halides with tetraalkylthiuram disulfides in water. The protocol allows easy access to C(sp3)–S bond formation, features the advantages of easy performance, environmental friendliness, good to excellent yields, and good functional tolerance, showing potential value for the preparation of some biologically active compounds.

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