Cas 391201-79-9,Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-bis(acetyloxy)-1-cyclohexen-1-yl]-, diethyl ester

391201-79-9

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Basic information

Product Name: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-bis(acetyloxy)-1-cyclohexen-1-yl]-, diethyl ester
Synonyms:
CAS NO:391201-79-9
Molecular Formula: C16H26NO8P
Molecular Weight: 391.358
EINECS: N/A
Product Categories: N/A

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-bis(acetyloxy)-1-cyclohexen-1-yl]-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-bis(acetyloxy)-1-cyclohexen-1-yl]-, diethyl ester(391201-79-9)
EPA Substance Registry System: Phosphonic acid, [(3R,4R,5S)-4-(acetylamino)-3,5-bis(acetyloxy)-1-cyclohexen-1-yl]-, diethyl ester(391201-79-9)

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: 391201-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 391201-79-9 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 391201-79:
(8*3)+(7*9)+(6*1)+(5*2)+(4*0)+(3*1)+(2*7)+(1*9)=129
129 % 10 = 9
So 391201-79-9 is a valid CAS Registry Number.

391201-79-9Upstream product

391201-79-9Downstream Products

391201-80-2 diethyl (3R,4R,5S)-4-acetamido-3,5-dihydroxy-1-cyclohexenephosphonate

391201-79-9Relevant 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 (2001)

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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