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Benzenecarbothioamide, N,N,2-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63385-19-3

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63385-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63385-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,8 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63385-19:
(7*6)+(6*3)+(5*3)+(4*8)+(3*5)+(2*1)+(1*9)=133
133 % 10 = 3
So 63385-19-3 is a valid CAS Registry Number.

63385-19-3Downstream Products

63385-19-3Relevant academic research and scientific papers

Sulfur promoted decarboxylative thioamidation of carboxylic acids using formamides as amine proxy

Kumar, Saurabh,Vanjari, Rajeshwer,Guntreddi, Tirumaleswararao,Singh, Krishna Nand

, p. 2012 - 2017 (2016/04/05)

An efficient decarboxylative thioamidation of arylacetic and cinnamic acids has been developed employing formamides as amine surrogate and sulfur as promoter. Thioamides with variant structural features are obtained under mild reaction conditions without the use of transition metal catalysts and oxidants.

Decarboxylative thioamidation of arylacetic and cinnamic acids: A new approach to thioamides

Guntreddi, Tirumaleswararao,Vanjari, Rajeshwer,Singh, Krishna Nand

supporting information, p. 3624 - 3627 (2014/08/05)

A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.

Copper(II)-catalyzed reactions of dimethylformamide with phenylacetonitrile and sulfur to form N,N-dimethylthioamides

Qu, Yanyang,Li, Zhengkai,Xiang, Haifeng,Zhou, Xiangge

supporting information, p. 3141 - 3146 (2013/12/04)

Novel copper-catalyzed three-component reactions of phenylacetonitrile, sulfur and DMF (dimethyformamide) for the selective preparation of N,N-dimethylthiobenzamide and N,N-dimethyl-2-phenylethanethioamides in yields of up to 96% are described. Copyright

Atroposelectivity of reactions of benzylic metalated thiobenzamides and thionaphthamides

Ach, David,Reboul, Vincent,Metzner, Patrick

, p. 3398 - 3406 (2007/10/03)

N,N-Dialkyl-2-methylbenzenecarbothioamides and naphthalenecarbothioamides were prepared by thionation of amides with Lawesson's reagent under unusual conditions. Their axial chirality was evidenced. Benzylic deprotonation of thioamides bearing N,N-diisopr

5-Alkylsulfinylbenzoyl- and 5-alkylsulfonylbenzoyl-1,2-dihydro-3H-pyrrolo[1,]pyrrole-1-carboxylic acids

-

, (2008/06/13)

Novel 5-alkylsulfinylbenzoyl- and 5-alkylsulfonylbenzoyl,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid compounds represented by the formula STR1 and the pharmaceutically acceptable, non-toxic esters and salts thereof, wherein n is 1 or 2, R is hydr

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