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735269-14-4

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735269-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 735269-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 735269-14:
(8*7)+(7*3)+(6*5)+(5*2)+(4*6)+(3*9)+(2*1)+(1*4)=174
174 % 10 = 4
So 735269-14-4 is a valid CAS Registry Number.

735269-14-4Downstream Products

735269-14-4Relevant articles and documents

T BuOK-triggered bond formation reactions

Xu, Yulong,Shi, Xiaonan,Wu, Lipeng

, p. 24025 - 24029 (2019)

Recently, inexpensive and readily available tBuOK has seen widespread use in transition-metal-free reactions. Herein, we report the use of tBuOK for S-S, S-Se, NN and CN bond formations, which significantly extends the scope of tBuOK in chemical synthesis. Compared with traditional methods, we have realized mild and general methods for disulfide, azobenzenes imine etc. synthesis.

Alternating Current Electrolysis for the Electrocatalytic Synthesis of Mixed Disulfide via Sulfur–Sulfur Bond Metathesis towards Dynamic Disulfide Libraries

Hilt, Gerhard,Otten, Chris Josef,Sattler, Lars Erik

supporting information, (2020/02/27)

A novel approach of electrolysis using alternating current was applied in the sulfur–sulfur bond metathesis of symmetrical disulfides towards unsymmetrical disulfides. As initially expected, a statistical distribution in disulfides was obtained. Furthermore, the influence of electrode polarisation by alternating current was investigated on a two-disulfide matrix. The highly dynamic nature of this chemistry resulted in the creation of dynamic disulfide libraries by expansion of the matrices, consisting of up to six symmetrical disulfides. In addition, mixing of matrices and stepwise expanding of a matrix by using alternating current electrolysis were realised.

A traceless, one-pot preparation of unsymmetric disulfides from symmetric disulfides through a repeated process involving sulfenic acid and thiosulfinate intermediates

Han, Minsoo,Lee, Jong Tak,Hahn, Hoh-Gyu

experimental part, p. 236 - 239 (2011/02/28)

A variable group of unsymmetric disulfides was prepared under mild reaction conditions and in high yields through the reaction of symmetric disulfides with sulfuryl chloride followed by treatment with thiols in the presence of water.

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