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(Z)-3-(4-Nitro-phenylsulfanyl)-3-phenyl-1-p-tolyl-propenone is a complex organic compound characterized by its unique molecular structure. It features a conjugated enone system with a phenyl group at the 3-position and a p-tolyl group (a methyl-substituted phenyl group) at the 1-position. The molecule also contains a 4-nitro-phenylsulfanyl group, which is a sulfanyl (-SH) group attached to a nitro-substituted phenyl ring. (Z)-3-(4-Nitro-phenylsulfanyl)-3-phenyl-1-p-tolyl-propenone is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its diverse functional groups and potential reactivity. Its specific applications would depend on its chemical properties, which could include reactivity with nucleophiles, electrophilic aromatic substitution, and Michael addition reactions, among others.

86175-44-2

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86175-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86175-44-2 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, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86175-44:
(7*8)+(6*6)+(5*1)+(4*7)+(3*5)+(2*4)+(1*4)=152
152 % 10 = 2
So 86175-44-2 is a valid CAS Registry Number.

86175-44-2Downstream Products

86175-44-2Relevant 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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