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2-(benzylsulfanyl)-1-methylethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374787-07-1

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1374787-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374787-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,7,8 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1374787-07:
(9*1)+(8*3)+(7*7)+(6*4)+(5*7)+(4*8)+(3*7)+(2*0)+(1*7)=201
201 % 10 = 1
So 1374787-07-1 is a valid CAS Registry Number.

1374787-07-1Downstream Products

1374787-07-1Relevant 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

Visible-Light-Mediated Thiol-Ene Reactions through Organic Photoredox Catalysis

Zhao, Gaoyuan,Kaur, Sarbjeet,Wang, Ting

supporting information, p. 3291 - 3294 (2017/06/23)

Synthetically useful radical thiol-ene reactions can be initiated by visible-light irradiation in the presence of an organic photocatalyst, 9-mesityl-10-methylacridinum tetrafluoroborate. The key thiyl radical intermediates are generated upon quenching of

A new synthetic route for the preparation of β-acyloxy mercaptans via the addition of thioacids to epoxides

Abbasi, Mohammad

experimental part, p. 2608 - 2610 (2012/07/02)

A new synthetic route for the preparation of S-benzylated β-acyloxy mercaptans starting from the one-pot reaction of thioacids and epoxides using a silica gel/Et3N combined catalyst is described. The thiol functionality in the crude product is then protected via benzylation and the corresponding thioethers are isolated after chromatography.

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