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N-[bis(dimethylamino)methylene]benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14667-95-9

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14667-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14667-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,6 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14667-95:
(7*1)+(6*4)+(5*6)+(4*6)+(3*7)+(2*9)+(1*5)=129
129 % 10 = 9
So 14667-95-9 is a valid CAS Registry Number.

14667-95-9Downstream Products

14667-95-9Relevant academic research and scientific papers

Novel coupling reaction between sulfonyl azide and N,N,N',N'-tetramethylthiourea

Aswad, Muhammad,Chiba, Junya,Hatanaka, Yasumaru,Tomohiro, Takenori

, p. 1611 - 1613 (2019)

The synthesis of sulfonylguanidines from N,N,N',N'-tetramethylthiourea and sulfonyl azides is described. This method serves as an alternative route for generating sulfonylguanidines via the use of stable starting materials.

Facile one-pot synthesis of tetrasubstituted N-sulfonylguanidines from sulfonamides and ureas

Wang, Fei,Yumaier, Abulimiti,Wusiman, Abudureheman

, p. 993 - 999 (2021/08/12)

A facile method for the synthesis of tetrasubstituted N-sulfonylguanidines has been developed via the direct condensation of sulfonamides and ureas in the presence of phosphoryl chloride under basic conditions. Detailed synthetic studies showed that this is a simple protocol for preparing N-sulfonylguanidines at room temperature in a short reaction time with good to excellent yields. Graphic abstract: [Figure not available: see fulltext.].

N -Sulfonyl acetylketenimine as a highly reactive intermediate for the synthesis of N -sulfonyl amidines

Yang, Weiguang,Huang, Dayun,Zeng, Xiaobao,Luo, Dongping,Wang, Xinyan,Hu, Yuefei

supporting information, p. 8222 - 8225 (2018/07/29)

A highly reactive intermediate N-sulfonyl acetylketenimine was generated from a 3-butyn-2-one participating CuAAC/ring-opening method. Its high reactivity due to bearing two EWGs allowed us to offer the first example of a reaction between ketenimine and amide to synthesize N-sulfonyl amidines efficiently.

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