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Ethyl 2-benzylthiomethylacrylate is a chemical compound with the molecular formula C14H16O2S. It is an organic ester derived from acrylic acid, featuring a benzylthiomethyl group attached to the double bond. ethyl 2-benzylthiomethylacrylate is characterized by its potential reactivity and is used in various chemical synthesis processes, particularly in the preparation of pharmaceuticals and other specialty chemicals. Its structure allows for a range of applications, including as an intermediate in the synthesis of complex organic molecules, due to its ability to participate in various types of chemical reactions such as addition, substitution, and elimination reactions.

783-11-9

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783-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 783-11-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 783-11:
(5*7)+(4*8)+(3*3)+(2*1)+(1*1)=79
79 % 10 = 9
So 783-11-9 is a valid CAS Registry Number.

783-11-9Relevant academic research and scientific papers

Method of manufacturing compds. Allylnaphthol

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Paragraph 0030-0032; 0039; 0042, (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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