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Z-3-methyl-but-1-en-1-yl phenyl sulphide is an organic compound characterized by its distinct chemical structure. It is a sulphur-containing molecule, specifically a sulphide, which is formed by the linkage of a phenyl group (C6H5) with a 3-methyl-but-1-en-1-yl group through a sulphur atom. The 3-methyl-but-1-en-1-yl group is a branched-chain alkene with a double bond between the first and second carbon atoms, and a methyl group attached to the third carbon. Z-3-methyl-but-1-en-1-yl phenyl sulphide is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science, due to its ability to form stable bonds and its reactivity with other molecules.

58431-65-5

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58431-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58431-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58431-65:
(7*5)+(6*8)+(5*4)+(4*3)+(3*1)+(2*6)+(1*5)=135
135 % 10 = 5
So 58431-65-5 is a valid CAS Registry Number.

58431-65-5Downstream Products

58431-65-5Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF ALKENYL SULPHIDES BY CROSS-COUPLING REACTIONS OF SECONDARY ALKYL GRIGNARD REAGENTS WITH Z- OR E-1-BROMO-2-PHENYLTHIOETHENE IN THE PRESENCE OF TRANSITION METAL CATALYSTS

Fiandanese, Vito,Miccoli, Giovanni,Naso, Francesco,Ronzini, Ludovico

, p. 343 - 348 (1986)

Z- and E-1-bromo-2-phenylthioethenes were cross-coupled stereospecifically with s-alkyl Grignard reagents in the presence of a series of NiII, PdII, or FeIII catalysts with the aim of finding a catalyst which would not cau

Homologation of aldehydes using (phenylthiomethylene) triphenylarsorane: Selective preparation of α-thiophenoxyepoxides and phenylthioenol ethers

Boubia,Mioskowski,Manna,Falck

, p. 6023 - 6026 (2007/10/02)

The title arsonium ylide reacts with aldehydes to give exclusively α-thiophenoxyepoxides in THF and phenylthioenol ethers in THF/HMPA. The former adducts are readily transformed to α-thiophenoxy carbonyls and the latter to one-carbon homologated aldehydes.

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