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methyl (2S,5E)-2-(tert-butoxycarbonylamino)-4-oxo-8-phenyloct-5-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1197335-53-7

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1197335-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197335-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,3,3 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1197335-53:
(9*1)+(8*1)+(7*9)+(6*7)+(5*3)+(4*3)+(3*5)+(2*5)+(1*3)=177
177 % 10 = 7
So 1197335-53-7 is a valid CAS Registry Number.

1197335-53-7Downstream Products

1197335-53-7Relevant academic research and scientific papers

Synthesis and reactivity of 4-oxo-5-trimethylsilanyl derived α-amino acids

Reid, Caroline M.,Fanning, Kate N.,Fowler, Lindsay S.,Sutherland, Andrew

, p. 245 - 251 (2015/02/02)

A Lewis-acid promoted one-carbon homologation of an aspartic acid semialdehyde with trimethylsilyldiazomethane has led to the efficient synthesis of two silicon-containing α-amino acids. The use of trimethylaluminium or catalytic tin(II) chloride gave nov

Synthesis of fluorescent enone derived α-amino acids

Fowler, Lindsay S.,Ellis, David,Sutherland, Andrew

experimental part, p. 4309 - 4316 (2009/12/06)

The development of a facile and general method for the preparation of enone derived α-amino acids is described. The key step involves a Horner-Wadsworth-Emmons reaction between an aspartic acid derived β-keto phosphonate ester and a range of aldehydes resulting in the formation of highly functionalised α-amino acids in good yields. An efficient two-stage deprotection process using mild conditions was developed to give the parent α-amino acids. Application of this methodology has produced a novel fluorescent α-amino acid that has potential as a biological marker.

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