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benzyl 2-hexylprop-2-en-1-yl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1309362-99-9

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1309362-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309362-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,3,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1309362-99:
(9*1)+(8*3)+(7*0)+(6*9)+(5*3)+(4*6)+(3*2)+(2*9)+(1*9)=159
159 % 10 = 9
So 1309362-99-9 is a valid CAS Registry Number.

1309362-99-9Downstream Products

1309362-99-9Relevant academic research and scientific papers

Method of manufacturing compds. Allylnaphthol

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Paragraph 0030-0032; 0038, (2018/06/26)

PROBLEM TO BE SOLVED: To provide a production method of an allyl compound of carrying out the dehydration allylation of a substrate having S, C or N which is a nucleophilic atom, especially S under the presence of a catalyst system consisting of a catalyst precursor having a specific structure and a specific ligand. SOLUTION: The production method of allyl compounds comprises as follow. A catalyst precursor chosen from Formula (1) and Formula (2) and a ligand are mixed, or a catalyst precursor, an allyl alcohol, and a ligand are mixed, then allyl alcohols and a substrate are blended and made to react. The ligand is quinaldic acid or picolinic acid, and the substrate is thiols, thiocarboxylic acids or the like. [Ru(C5H5)(CH3CN)3]PF6(1). [Ru[C5(CH3)5](CH3CN)3]PF6(2). COPYRIGHT: (C)2012,JPOandINPIT

Highly efficient catalytic dehydrative S-allylation of thiols and thioic S-acids

Tanaka, Shinji,Pradhan, Prasun Kanti,Maegawa, Yusuke,Kitamura, Masato

supporting information; experimental part, p. 3996 - 3998 (2010/07/06)

A SH-selective allylation method using [CpRu(2-quinolinecarboxylato) (η3-C3H5)]PF6 has been realized in various solvents including aqueous media to give allyl sulfides and allyl S-thioates, demonstrating the potential applicability to lipopeptide chemistry.

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