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17709-95-4

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17709-95-4 Usage

Synthesis Reference(s)

Tetrahedron Letters, 21, p. 4061, 1980 DOI: 10.1016/0040-4039(80)88066-X

Check Digit Verification of cas no

The CAS Registry Mumber 17709-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,0 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17709-95:
(7*1)+(6*7)+(5*7)+(4*0)+(3*9)+(2*9)+(1*5)=134
134 % 10 = 4
So 17709-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NS/c1-11(2)10(12)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3

17709-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-2-phenylethanethioamide

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-(2-phenyl)ethanethioamide

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:17709-95-4 SDS

17709-95-4Relevant articles and documents

A facile access to thieno[2,3-b]indoles via sulfur-mediated decarboxylative cyclization of α, β-unsaturated carboxylic acids with indoles

Zhang, Hao-Lin,Wen, Fei,Sheng, Wen-Bing,Yin, Peng,Zhang, Chun-Tao,Peng, Cai-Yun,Peng, Dong-Ming,Liao, Duan-Fang,Fu, Rong-Geng

, p. 80 - 83 (2019)

An efficient synthesis of thieno[2,3-b]indoles via a one-pot three-component reaction was well established. By using inexpensive and commercial available indoles and α, β-unsaturated carboxylic acids in the presence of elemental sulfur, various functional groups were achieved in moderate to good yields.

The thioamidation ofgem-dibromoalkenes in an aqueous medium

Vankar, Jigarkumar K.,Gupta, Ankush,Jadav, Jaydeepbhai P.,Nanjegowda, Shankara H.,Gururaja, Guddeangadi N.

, p. 2473 - 2480 (2021/04/02)

The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium. The presented green protocol emphasizes the suitability of aqueous media for the thioamidation reaction and enables greater selectivity with synthetic utility. A wide range of thioamides in moderate to excellent yields has been achieved using readily available starting materials, with the use of no organic solvents, catalysts, or additives.

Solvent-controlled highly regio-selective thieno[2,3-: B] indole formation under metal-free conditions

Ni, Penghui,Li, Bin,Huang, Huawen,Xiao, Fuhong,Deng, Guo-Jun

supporting information, p. 5553 - 5558 (2017/12/06)

An efficient three-component thieno[2,3-b]indole formation method was developed under metal-free conditions. The cascade cyclization was enabled by acid-promoted annulation of indoles, ketones and sulfur powder, which enabled modular synthesis of 2-substituted and 3-substituted thieno[2,3-b]indoles with excellent regioselectivity and broad functional group tolerance. DMF solvent played an important role in the regioselectivity control.

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