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2-((S)-1-Phenyl-ethylamino)-3-phosphono-propionic acid is a complex organic compound with the molecular formula C11H14NO4P. It is a chiral molecule, with the (S)-configuration indicating that it is the levorotatory enantiomer. 2-((S)-1-Phenyl-ethylamino)-3-phosphono-propionic acid features a phenylethylamine group attached to a phosphonopropionic acid backbone, which is characterized by the presence of a phosphonic acid group (-PO3H2). The structure consists of a phenyl ring, an ethylamine chain, and a phosphonopropionic acid segment, which together contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

86554-28-1

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86554-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86554-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,5 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86554-28:
(7*8)+(6*6)+(5*5)+(4*5)+(3*4)+(2*2)+(1*8)=161
161 % 10 = 1
So 86554-28-1 is a valid CAS Registry Number.

86554-28-1Relevant academic research and scientific papers

PREPARATION D'ACIDES AMINOCARBOXY-ALKYLPHOSPHONIQUES OPTIQUEMENT ACTIFS

Villanueva, J. M.,Collignon, N.,Guy, A.,Savignac, Ph.

, p. 1299 - 1306 (2007/10/02)

In aqueous solution ω-formylalkylphosphonates in the presence of hydrogen cyanide and (S) (-) α-methylbenzylamine give optically active aminonitriles with an enantiomeric excess of 50percent.Phosphonic aminonitriles are submitted to acid hydrolysis, then esterified and debenzylated without any epimerization.The separation is performed either with the acid or with the ester.All the operations are monitored by NMR (1H, 13C, 31P) and whenever possible, by GC.

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