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120517-31-9

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120517-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120517-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120517-31:
(8*1)+(7*2)+(6*0)+(5*5)+(4*1)+(3*7)+(2*3)+(1*1)=79
79 % 10 = 9
So 120517-31-9 is a valid CAS Registry Number.

120517-31-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylsulfanyl-1H-indole

1.2 Other means of identification

Product number -
Other names 2-phenylthio-1H-indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120517-31-9 SDS

120517-31-9Relevant articles and documents

TFA-promoted direct C-H sulfenylation at the C2 position of non-protected indoles

Hostier, Thomas,Ferey, Vincent,Ricci, Gino,Pardo, Domingo Gomez,Cossy, Janine

, p. 13898 - 13901 (2015)

A simple, efficient and practical metal-free C-H sulfenylation process at the C2 position of non-protected indoles has been developed. 2-Thioindoles were obtained in moderate to high yields using stable and readily available N-(thio)succinimides at room temperature in the presence of TFA.

Intramolecular Hydroamination of Selenoalkynes to 2-Selenylindoles in the Absence of Catalyst

Coelho, Felipe L.,Gil, Eduarda S.,Gon?alves, Paulo F. B.,Campo, Leandra F.,Schneider, Paulo H.

, p. 8157 - 8162 (2019)

In this work, a series of 2-chalcogenylindoles was synthesized by an efficient methodology, starting from chalcogenoalkynes, including a previously unreported tellurium indole derivative. For the first time, these 2-substituted chalcogenylindoles were obtained in the absence of metal catalyst or base, under thermal conditions only. In addition, the results described herein represent a methodology with inverse regioselectivity for the chalcogen functionalization of indoles.

Synthesis of 2-(Arylthio)indolenines via Chemoselective Arylation of Thio-Oxindoles with Arynes

Saputra, Adi,Fan, Rong,Yao, Tuanli,Chen, Jian,Tan, Jiajing

, p. 2683 - 2688 (2020/05/18)

A chemoselective S-arylation reaction of thio-oxindoles with arynes is presented. The reaction was performed under mild conditions and provided a straightforward synthesis of 2-(arylthio)indolenines in good to excellent yields. Besides, this simple operat

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