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3-Buten-1-ol, 4-(phenylthio)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112471-71-3

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112471-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112471-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112471-71:
(8*1)+(7*1)+(6*2)+(5*4)+(4*7)+(3*1)+(2*7)+(1*1)=93
93 % 10 = 3
So 112471-71-3 is a valid CAS Registry Number.

112471-71-3Downstream Products

112471-71-3Relevant academic research and scientific papers

Metal-free photocatalytic thiol-ene/thiol-yne reactions

Kaur, Sarbjeet,Zhao, Gaoyuan,Busch, Evan,Wang, Ting

supporting information, p. 1955 - 1961 (2019/02/20)

The organic photocatalyst (9-mesityl-10-methylacridinum tetrafluoroborate) in the presence of visible light is used to initiate thiol-ene and thiol-yne reactions. Thiyl radicals are generated upon quenching the photoexcited catalyst with a range of thiols

Air Oxidative Radical Oxysulfurization of Alkynes Leading to α-Thioaldehydes

Zhou, Shao-Fang,Pan, Xiang-Qiang,Zhou, Zhi-Hao,Shoberu, Adedamola,Zhang, Pei-Zhi,Zou, Jian-Ping

, p. 5348 - 5354 (2015/05/27)

Air oxidative radical oxysulfurization of alkynes initiated by 0.5 mol % tert-butyl hydroperoxide with arylthiols is described. The reaction proceeded at room temperature in the presence of 5% mol water to afford selective α-thioaldehydes. (Chemical Equation Presented).

Ruthenium-catalyzed cross-metathesis with electron-rich phenyl vinyl sulfide enables access to 2,3-dideoxy-d-ribopyranose ring system donors

Boutureira, Omar,Isabel Matheu,Diaz, Yolanda,Castillon, Sergio

, p. 19794 - 19799 (2014/05/20)

2,3-Dideoxy-d-ribopyranose units are important ring systems found in nature. Herein, we develop a metal-mediated strategy to form this important scaffold featuring a cross-metathesis reaction of the corresponding sugar-derived hydroxyalkene with electron-

Synthesis of vinyl sulfides under base-free conditions using selenium ionic liquid

Thurow, Samuel,Ostosi, Naiana T.,Mendes, Samuel R.,Jacob, Raquel G.,Lenard?o, Eder J.

experimental part, p. 2651 - 2653 (2012/06/30)

A very simple procedure is described for the efficient synthesis of vinyl sulfides by hydrothiolation of terminal alkynes using 1-n-butyl-3- methylimidazolium methylselenite, [bmim][SeO2(OCH3)]. The reaction proceeds cleanly under mi

Synthesis of vinyl sulfides using glycerol as a recyclable solvent

Lenardao, Eder J.,Silva, Marcio S.,Lara, Renata G.,Marczewski, Junior M.,Sachini, Maraisa,Jacob, Raquel G.,Alves, Diego,Perin, Gelson

experimental part, p. 272 - 282 (2011/05/13)

A new, clean, and efficient protocol is described for the hydrothiolation of terminal alkynes promoted by KF/Al2O3, using glycerol as recyclable solvent. This improved method furnishes selectively the corresponding anti-Markovnikov v

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