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(Z)-3-(4-Bromo-phenyl)-1-phenyl-3-p-tolylsulfanyl-propenone is a complex organic chemical compound characterized by its unique molecular structure. It is a derivative of chalcone, featuring a 1,3-diaryl-2-propen-1-one backbone with a bromine atom at the para position of the phenyl ring, a p-tolylthio group attached to the carbonyl carbon, and a phenyl group at the 1-position. (Z)-3-(4-Bromo-phenyl)-1-phenyl-3-p-tolylsulfanyl-propenone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its diverse functional groups and reactivity. The presence of the bromine atom makes it a valuable intermediate for further functionalization, while the p-tolylthio group introduces sulfur into the molecule, which can influence its chemical properties and reactivity.

86175-34-0

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86175-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86175-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86175-34:
(7*8)+(6*6)+(5*1)+(4*7)+(3*5)+(2*3)+(1*4)=150
150 % 10 = 0
So 86175-34-0 is a valid CAS Registry Number.

86175-34-0Downstream Products

86175-34-0Relevant academic research and scientific papers

NUCLEOPHILIC THIYLATION OF DIARYLPROPYNONES. STEREOCHEMISTRY OF THE REACTION

Statsyuk, V. E.,Krasnov, V. L.,Korshunov, S. P.,Bodrikov, I. V.

, p. 408 - 414 (2007/10/02)

The stereochemical aspects of the reactions of diarylpropynones with alkali-metal thiolates and thiols activated by amines were investigated.The ratio between the adducts with the Z and E configurations under conditions with kinetic control and the config

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