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(R,S)-allenyl-phenylalanine is a unique amino acid derivative characterized by the presence of an allene group (a carbon-carbon double bond with an adjacent carbon-carbon single bond) attached to the side chain of phenylalanine. (R,S)-allenyl-phenylalanine exhibits an interesting combination of properties due to the presence of both the allene and phenyl groups, which can lead to distinct chemical reactivity and biological activity compared to the parent amino acid. The (R,S) notation indicates that the compound exists as a mixture of two diastereomers, each with a different configuration at the chiral center. This chiral complexity can further influence its interactions with biological targets and its potential applications in medicinal chemistry and materials science.

92136-52-2

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92136-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92136-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92136-52:
(7*9)+(6*2)+(5*1)+(4*3)+(3*6)+(2*5)+(1*2)=122
122 % 10 = 2
So 92136-52-2 is a valid CAS Registry Number.

92136-52-2Downstream Products

92136-52-2Relevant academic research and scientific papers

SYNTHESIS OF α-AMINO ACIDS WITH β,γ-UNSATURATED SIDE CHAINS

Castelhano, Arlindo L.,Horne, Stephen,Taylor, Gregg J.,Billedeau, Roland,Krantz, Allen

, p. 5451 - 5466 (2007/10/02)

α-Amino acids with allenyl, vinyl and acetylenic side chains can be synthesized using non-enolate based strategies.The ester enolate-Claisen rearrangement applied to propargylic esters of N-protected α-amino acids is of limited utility since only poor yields of allenic product are obtained with the N-Boc glycine esters, the system which give the most reproducible results.However, α-allenyl-α-amino acids that are fully functionalized on the α-carbon are available through the agency of 4-allenyl-2-phenyloxazolones 4 ( obtained from propargyl esters of N-benzoyl protected amino acids via cyclization and Claisen rearrangement ) provided that Meerwein's reagent is used to facilitate hydrolysis of the benzamide function in 5.A variety of α-substituted glycinates, including those with α-vinyl and α-acetylenic functions, can be prepared using a two step sequence involving condensation of the cationic glycine synthon 22 with various organomagnesium reagents, followed by hydrolysis.

α-allenic-α-amino acids as enzyme inhibitors

-

, (2008/06/13)

Novel α-allenic-α-amino acids which are enzyme inhibitors of the suicide or kcat type are disclosed herein.

GENERAL SYNTHETIC ACCESS TO α-ALLENYL AMINES AND α-ALLENYL-α-AMINOACIDS AS POTENTIAL ENZYME ACTIVATED IRREVERSIBLE INHIBITORS OF PLP DEPENDENT ENZYMES

Casara, Patrick,Jund, Karin,Bey, Philippe

, p. 1891 - 1894 (2007/10/02)

The entitled allene derivatives have been prepared from the parent α-ethynyl amines and α-amino acids.The corresponding derivative of GABA, putrescine and phenylalanine have been found to be irreversible and time dependent inhibitors of GABA-T, ODC and ba

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