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(Z)-2-Phenyl-3-phenylsulfanyl-prop-2-en-1-ol is an organic compound characterized by its unique molecular structure. It is a chiral molecule, with the "Z" configuration indicating that the phenyl and phenylsulfanyl groups are on the same side of the double bond. (Z)-2-Phenyl-3-phenylsulfanyl-prop-2-en-1-ol is a derivative of phenol, featuring a phenyl group attached to a prop-2-en-1-ol backbone, which is further modified by a phenylsulfanyl group. The presence of the phenylsulfanyl group introduces a sulfur-phenyl bond, which can influence the compound's reactivity and physical properties. It is a colorless liquid with a distinct aromatic odor, and its chemical properties are shaped by the interaction between the phenyl rings and the sulfanyl group. (Z)-2-Phenyl-3-phenylsulfanyl-prop-2-en-1-ol is of interest in organic chemistry, potentially for its applications in the synthesis of pharmaceuticals, agrochemicals, or as a precursor in the production of other organic compounds.

87295-69-0

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87295-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87295-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,9 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87295-69:
(7*8)+(6*7)+(5*2)+(4*9)+(3*5)+(2*6)+(1*9)=180
180 % 10 = 0
So 87295-69-0 is a valid CAS Registry Number.

87295-69-0Downstream Products

87295-69-0Relevant academic research and scientific papers

Applications des reactifs de Grignard vinyliques γ-functionnels a la synthese de nouveaux composes soufres

Doboudin, Jean-Georges,Jousseaume, Bernard,Thoumazeau, Elisabeth

, p. 105 - 108 (2007/10/02)

In previous publications we had examined synthetic methods involving new γ-functional vinylic Grignard reagents 1 and their reactivities toward halogenated and carbonyl derivatives.Since numerous synthetic applications of α,β- and β,γ-unsaturated sulfur c

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