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(4R)-4-(2,2-bis(phenylsulfonyl)ethyl)-2-tert-butyl-4-phenyloxazol-5(4H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1233532-30-3

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1233532-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233532-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,5,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1233532-30:
(9*1)+(8*2)+(7*3)+(6*3)+(5*5)+(4*3)+(3*2)+(2*3)+(1*0)=113
113 % 10 = 3
So 1233532-30-3 is a valid CAS Registry Number.

1233532-30-3Downstream Products

1233532-30-3Relevant academic research and scientific papers

Enantioselective organocatalytic addition of oxazolones to 1,1-bis(phenylsulfonyl)ethylene: A convenient asymmetric synthesis of quaternary α-amino acids

Alba, Andrea-Nekane R.,Companyo, Xavier,Valero, Guillem,Moyano, Albert,Rios, Ramon

, p. 5354 - 5361 (2010)

A new, easy, and highly enantioselective method for the synthesis of quaternary α-alkyl-α-amino acids based on organocatalysis is reported. The addition of oxazolones to 1, 1-bis(phenylsulfonyl)ethylene is efficiently catalyzed by simple chiral bases or thioureas. The reaction affords α-disubstituted α-amino acid derivatives with complete C4 regioselectivity and with excellent yields and enantioselectivities. This methodology is complementary to previously reported enantioselec-tive approaches to quaternary ot-amino acids and allows the synthesis of αphenyl-α- alkyl-α-amino acids and αiert-butyl-α-alky1-α-amino acids. It has distinct advantages in terms of operational simplicity, enviromentally friendly conditions, and suitability for largescale reactions.

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