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(2S)-2-[(benzyloxycarbonyl)amino]-3-(4-decyloxyphenyl)propanoic acid is a complex organic compound with the molecular formula C27H37NO5. It is a chiral molecule, denoted by the "2S" prefix, indicating the presence of a stereocenter with the S configuration. The compound features a benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to protect the amino group. It also contains a 4-decyloxyphenyl moiety, which is a phenyl ring with a decyloxy (C10H21O) substituent at the para position. (2S)-2-[(benzyloxycarbonyl)amino]-3-(4-decyloxyphenyl)propanoic acid is likely used in the synthesis of pharmaceuticals or other bioactive molecules, where the Cbz group can be removed under specific conditions to reveal the free amino group, and the decyloxyphenyl group may contribute to the compound's biological activity or solubility properties.

87190-92-9

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87190-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87190-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,9 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87190-92:
(7*8)+(6*7)+(5*1)+(4*9)+(3*0)+(2*9)+(1*2)=159
159 % 10 = 9
So 87190-92-9 is a valid CAS Registry Number.

87190-92-9Relevant academic research and scientific papers

Novel non-peptide GPIIb/IIIa antagonists: Synthesis and biological activities of 2-[4-[2-(4-amidinobenzoylamino)-2-(substituted)acetyl]-3-(2-methoxy-2- oxoethyl)-2-oxopiperazinyl] acetic acids

Kitamura,Fukushi,Miyawaki,Kawamura,Terashita,Sugihara,Naka

, p. 258 - 267 (2007/10/03)

To improve the in vitro and in vivo potency of our first low molecular weight GPIIb/IIIa antagonist 1 (TAK-029), a series of 2-[4-[2-(4-amidinobenzoylamino)-2-(substituted)acetyl]-3-(2-methoxy-2- oxoethyl)-2-oxopiperazinyl]acetic acids were synthesized th

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