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2-((S)-1-Phenyl-ethylamino)-4-phosphono-butyric acid is a complex organic compound with the molecular formula C12H16NO4P. It is a chiral molecule, with the "S" configuration indicating that it is the (-)-enantiomer. 2-((S)-1-Phenyl-ethylamino)-4-phosphono-butyric acid is characterized by a phenylethylamine group attached to a butyric acid backbone, which is further modified by a phosphonic acid group. The presence of the phosphonic acid group imparts unique properties to the molecule, such as potential affinity for metal ions and possible applications in medicinal chemistry or as a chiral ligand in asymmetric synthesis. The compound's structure and properties make it a subject of interest in various fields, including pharmaceuticals and materials science, where it could be explored for its potential therapeutic effects or as a building block for more complex molecules.

86554-29-2

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86554-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86554-29-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 86554-29:
(7*8)+(6*6)+(5*5)+(4*5)+(3*4)+(2*2)+(1*9)=162
162 % 10 = 2
So 86554-29-2 is a valid CAS Registry Number.

86554-29-2Relevant 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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