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(E)-S-butyl 5-phenylpent-2-enethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1332505-48-2

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1332505-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332505-48-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,5,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1332505-48:
(9*1)+(8*3)+(7*3)+(6*2)+(5*5)+(4*0)+(3*5)+(2*4)+(1*8)=122
122 % 10 = 2
So 1332505-48-2 is a valid CAS Registry Number.

1332505-48-2Downstream Products

1332505-48-2Relevant articles and documents

Ruthenium-catalyzed rearrangement of propargyl sulfoxides: Formation of α,β-unsaturated thioesters

Zheng, Renhua,Wang, Youliang,Zhang, Liming

, p. 3144 - 3146 (2015)

Our previously developed strategy of generating ketene intermediates via Ru-catalyzed intramolecular oxidation of terminal alkynes is applied to propargyl sulfoxides. The reaction undergoes interesting further rearrangement upon the ketene generation to a

Conjugate reduction and reductive aldol cyclization of α,β- unsaturated thioesters catalyzed by (BDP)CuH

Li, Ninglin,Ou, Jun,Miesch, Michel,Chiu, Pauline

supporting information; experimental part, p. 6143 - 6147 (2011/10/08)

A conjugate reduction of α,β-unsaturated thioesters catalyzed by copper hydride using PMHS as stoichiometric reductant has been developed. 1,2-Bis(diphenylphosphino)benzene (BDP) was the most effective ligand for this reduction. Saturated thioesters could be produced in excellent yields when the substituent on the thiol is not sterically-demanding. This protocol was applied to induce the reductive aldol cyclization of keto-enethioates, which could offer β-hydroxythioesters in moderate to good yields.

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