Cas 391201-80-2,Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-dihydroxy-1-cyclohexen-1-yl]-, diethyl ester

391201-80-2

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Basic information

Product Name: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-dihydroxy-1-cyclohexen-1-yl]-, diethyl ester
Synonyms:
CAS NO:391201-80-2
Molecular Formula: C12H22NO6P
Molecular Weight: 307.284
EINECS: N/A
Product Categories: N/A
Mol File: 391201-80-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-dihydroxy-1-cyclohexen-1-yl]-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-dihydroxy-1-cyclohexen-1-yl]-, diethyl ester(391201-80-2)
EPA Substance Registry System: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-dihydroxy-1-cyclohexen-1-yl]-, diethyl ester(391201-80-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 391201-80-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 391201-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,1,2,0 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 391201-80:
(8*3)+(7*9)+(6*1)+(5*2)+(4*0)+(3*1)+(2*8)+(1*0)=122
122 % 10 = 2
So 391201-80-2 is a valid CAS Registry Number.

391201-80-2Upstream product

391201-79-9 diethyl (3R,4R,5S)-4-acetamido-3,5-di-acetoxy-1-cyclohexenephosphonate

391201-80-2Downstream Products

391201-80-2Relevant academic research and scientific papers

Synthesis of L-xylose derived cyclohexenephosphonates - Versatile precursors of sialidase inhibitor libraries

Streicher, Hansj?rg,Meisch, J?ns,Bohner, Christoph

, p. 8851 - 8859 (2007/10/03)

L-xylo Configured cyclohexenephosphonates 1 and 2 have been synthesized as scaffolds for sialidase inhibitor libraries. These compounds were obtained by chain elongation and cyclization of suitably protected L-xylose. An unexpected phosphorylation was obs

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