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methyl α-benzoyl-α-phenylthiopropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82111-71-5

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82111-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82111-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82111-71:
(7*8)+(6*2)+(5*1)+(4*1)+(3*1)+(2*7)+(1*1)=95
95 % 10 = 5
So 82111-71-5 is a valid CAS Registry Number.

82111-71-5Relevant academic research and scientific papers

Reactions of Benzenesulphenyl Chloride with α,β-Unsaturated Compounds: Part II - Role of Steric Factors on Stability of Intermediates

Bhongle, N. N.,Gogte, V. N.

, p. 632 - 636 (2007/10/02)

In presence of pyridine, benzenesulfphenyl chloride (1) adds on the methyl α- and β-methyl crotonates and methyl α- and β-methyl cinnamates (6-9) in regiospecific manner involving an onium intermediate such as (18).The product pattern is decided by the st

Preparation and Diels-Alder Reactions of 1,1-Dicarbonylalkanes

Hoye, Thomas R.,Caruso, Andrew J.,Magee, Andrew S.

, p. 4152 - 4156 (2007/10/02)

1,1-Dicarbonyl- (ester, ketone, lactone) substituted alkenes are prepared from the corresponding saturated 1-phenylsulfinyl derivatives.These are formed from precursor sulfides, which can be efficiently prepared either by oxidation of β-hydroxy-α-phenylsulfenylcarbonyl compounds or direct acylation of α-phenylsulfenyl enolate anions with acid chlorides.Some of the title compounds can be isolated and then reacted while others are generated and reacted in situ in a Diels-Alder fashion with cyclopentadiene.Endo-exo selectivities are discussed.

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