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1622221-69-5

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1622221-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1622221-69-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,2,2,2 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1622221-69:
(9*1)+(8*6)+(7*2)+(6*2)+(5*2)+(4*2)+(3*1)+(2*6)+(1*9)=125
125 % 10 = 5
So 1622221-69-5 is a valid CAS Registry Number.

1622221-69-5Downstream Products

1622221-69-5Relevant articles and documents

Preparation method of indole sulfide compound

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Paragraph 0104-0108, (2019/05/08)

The invention discloses a preparation method of an indole sulfide compound. The preparation method is conducted according to the following steps that a catalyst, an indole reactant, hydrazine hydrate,substituted phenyl sulfonyl chloride and a solvent are

Photocatalytic direct C-S bond formation: Facile access to 3-sulfenylindoles: Via metal-free C-3 sulfenylation of indoles with thiophenols

Guo, Wei,Tan, Wen,Zhao, Mingming,Tao, Kailiang,Zheng, Lv-Yin,Wu, Yongquan,Chen, Deliang,Fan, Xiao-Lin

, p. 37739 - 37742 (2017/08/18)

An efficient and convenient photocatalytic direct C-3 sulfenylation of indoles with thiophenols has been developed for the construction of 3-sulfenylations. This protocol employs thiophenols as the sulfenylating agents, inexpensive rose bengal as the photocatalyst, and shows mild conditions, readily available starting materials, high atom and step atom economy, and environmental advantages. The representative method provides a straightforward approach for C-S bond formation, and has potential applications in the chemical and pharmaceutical industries.

N-Hydroxy sulfonamides as new sulfenylating agents for the functionalization of aromatic compounds

Wang, Fu-Xiang,Zhou, Shao-Da,Wang, Chengming,Tian, Shi-Kai

supporting information, p. 5284 - 5288 (2017/07/10)

An unprecedented use of N-hydroxy sulfonamides as sulfenylating agents has been established. In the presence of catalytic amounts of iodine and N-hydroxysuccinimide, N-hydroxy sulfonamides participated in sulfenylation with indoles, 7-azaindole, N-methyl pyrrole, and 2-naphthol to afford structurally diverse thioethers in moderate to excellent yields with very high regioselectivity.

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