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(2S)-2-Benzamido-2-methylbutanoic acid is a chiral organic compound with the molecular formula C12H15NO4. It is a derivative of 2-methylbutanoic acid, featuring a benzamide group attached to the 2nd carbon. (2S)-2-benzamido-2-methylbutanoic acid is characterized by its asymmetric carbon atom (the 2nd carbon), which gives it two enantiomeric forms, with the (2S)-isomer being the one specified. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and biologically active molecules due to its unique structural properties. The compound's specific stereochemistry and functional groups make it a valuable building block in the development of new drugs and other chemical products.

2583-47-3

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2583-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2583-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2583-47:
(6*2)+(5*5)+(4*8)+(3*3)+(2*4)+(1*7)=93
93 % 10 = 3
So 2583-47-3 is a valid CAS Registry Number.

2583-47-3Downstream Products

2583-47-3Relevant 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

experimental part, p. 5354 - 5361 (2010/09/15)

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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