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Benzene, 1-methyl-4-[(methylthio)ethynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17293-64-0

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17293-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17293-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,9 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17293-64:
(7*1)+(6*7)+(5*2)+(4*9)+(3*3)+(2*6)+(1*4)=120
120 % 10 = 0
So 17293-64-0 is a valid CAS Registry Number.

17293-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl)ethynyl methyl sulfide

1.2 Other means of identification

Product number -
Other names (p-Tolyl-ethinyl)-methylsulfid

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:17293-64-0 SDS

17293-64-0Relevant academic research and scientific papers

Aminoxylation of Thioalkynes through Radical-Polar Crossover

Di Mauro, Giovanni,Drescher, Martina,Maulide, Nuno,Tkaczyk, Sara

, p. 592 - 594 (2020)

A one-pot procedure for the aminoxylation of thioalkynes for the direct formation of α-functionalized thioesters under mild reaction conditions is reported. A ketenethionium ion is the key intermediate, which is generated in situ by Bronsted acid mediated protonation and undergoes a radical-polar crossover.

Accessing the Rare Diazacyclobutene Motif

Narangoda, Chandima J.,Lex, Timothy R.,Moore, Madelyn A.,McMillen, Colin D.,Kitaygorodskiy, Alex,Jackson, James E.,Whitehead, Daniel C.

supporting information, p. 8009 - 8013 (2019/01/04)

A formal [2 + 2] cycloaddition of 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) with electron-rich alkynyl sulfides and selenides is described. These investigations provide a convenient method to access diazacyclobutenes in good yield while tolerating a rela

One-pot preparation of arylethynyl sulfides and bis(arylethynyl) sulfides

Su, Qiong,Zhao, Zi-Jian,Xu, Feng,Lou, Peng-Cai,Zhang, Kai,Xie, De-Xun,Shi, Lei,Cai, Qing-Yun,Peng, Zhi-Hong,An, De-Lie

, p. 1551 - 1557 (2013/04/23)

An efficient preparation for arylethynyl sulfides 1 and bis(arylethynyl) sulfides 2 has been accomplished through a one-pot, three-step strategy that starts from arylethanonyl sulfides and bis(arylethanonyl) sulfides, respectively, without the use of various terminal arylacetylenes as substrates. When lithium hexamethyldisilazane (LHMDS), ClP(O)(OEt)2, and LHMDS were sequentially added to a tetrahydrofuran solution of different substrates [arylethanonyl sulfides or bis(arylethanonyl) sulfides], 1 or 2 were obtained in moderate to good yields. The reaction procedure involves the formation of an enol phosphate and a subsequent base-induced elimination. An efficient preparation of arylethynyl sulfides 1 and bis(arylethynyl) sulfides 2 has been accomplished by a one-pot, three-step strategy that starts from arylethanonyl sulfides and bis(arylethanonyl) sulfides, respectively, to give 1 and 2 in moderate to good yields. The reaction mechanism involves the formation of an enol phosphate that undergoes a subsequent base-induced elimination. Copyright

PYROLYSIS OF α-ACYL,α-THIO PHOSPHORANES THIOACETYLENES

Braga, Antonio L.,Comasseto, Joao V.,Petragnani, Nicola

, p. 1111 - 1114 (2007/10/02)

Pyrolysis of α-acyl,α-thio phosphoranes affords thioacetylenes in a good yield.The thio acethylenes are precursors of terminal and alkyl disubstituted acetylenes.

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