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72116-31-5

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72116-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72116-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,1 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72116-31:
(7*7)+(6*2)+(5*1)+(4*1)+(3*6)+(2*3)+(1*1)=95
95 % 10 = 5
So 72116-31-5 is a valid CAS Registry Number.

72116-31-5Downstream Products

72116-31-5Relevant academic research and scientific papers

Willgerodt-Kindler reaction at room temperature: Synthesis of thioamides from aromatic aldehydes and cyclic secondary amines

Kale, Arun D.,Tayade, Yogesh A.,Mahale, Sachin D.,Patil, Rahul D.,Dalal, Dipak S.

, (2019/09/12)

A simple method for the synthesis of thioamide derivatives in DMSO at room temperature and at 120 °C has been developed. Total 27 compounds were prepared under both conditions via a one-pot, three component reaction between substituted aromatic aldehydes,

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.

Substituted 1,4,2-Dithiazines: Synthesis by Ring Expansion of 1,3-Dithiolium Cations, Solution Redox Properties and X-Ray Crystal Structures of a Monocyclic and a Bicyclic Derivative

Bryce, Martin R.,Davison, Gordon R.,Batsanov, Andrei S.,Howard, Judith A. K.

, p. 2295 - 2302 (2007/10/02)

A range of derivatives of the 8 ?-electron 1,4,2-dithiazine system, viz. compounds 11a-d and 19-24, have been synthesized by ring expansion of the corresponding 1,3-dithiolium salts 8a-d and 13-18, respectively, using a mixture of iodine and aqueous ammon

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