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1253299-13-6

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1253299-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1253299-13-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,2,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1253299-13:
(9*1)+(8*2)+(7*5)+(6*3)+(5*2)+(4*9)+(3*9)+(2*1)+(1*3)=156
156 % 10 = 6
So 1253299-13-6 is a valid CAS Registry Number.

1253299-13-6Relevant articles and documents

Aerobic Visible-Light Induced Intermolecular S?N Bond Construction: Synthesis of 1,2,4-Thiadiazoles from Thioamides under Photosensitizer-Free Conditions

Wang, Hui,Xie, Shihua,Zhu, Hongjun,Zhuo, Liang

, p. 3398 - 3402 (2021/06/25)

Aerobic visible-light induced intermolecular S?N bond construction has been achieved without the addition of photosensitizer, metal, or base. With this strategy, 1,2,4-thiadiazoles can be obtained from thioamides. Preliminary mechanistic investigation suggested that the excited state of thioamides undergoes a single-electron-transfer (SET) process to afford thioamidyl radicals, which can be further transformed into a 1,2,4-thiadiazole through desulfurization and oxidative cyclization. The reaction has good functional group tolerance and represents a green method for the construction of S?N bonds.

Electrochemical Synthesis of 3,5-Disubstituted-1,2,4-thiadiazoles through NH4I-Mediated Dimerization of Thioamides

Wang, Zi-Qiang,Meng, Xiu-Jin,Li, Qian-Yu,Tang, Hai-Tao,Wang, Heng-Shan,Pan, Ying-Ming

supporting information, p. 4043 - 4048 (2018/09/21)

A electrochemical method for the synthesis of 3,5-disubstituted-1,2,4-thiadiazoles through NH4I-mediated dimerization of thioamides is reported. Using the inexpensive NH4I as electrolyte and catalyst, this electrosynthesis approach requires no oxidizing agents and enables the convenient production of diverse 1,2,4-thiadiazoles products. The approach is an example of S?N bond construction through the electrochemical method. (Figure presented.).

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