Cas 582295-50-9,Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-cyclohexanecarbonyl-tetrahydro-pyran-4-yl ester

582295-50-9

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Basic information

Product Name: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-cyclohexanecarbonyl-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:582295-50-9
Molecular Formula:
Molecular Weight: 441.478
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: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-cyclohexanecarbonyl-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-cyclohexanecarbonyl-tetrahydro-pyran-4-yl ester(582295-50-9)
EPA Substance Registry System: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-cyclohexanecarbonyl-tetrahydro-pyran-4-yl ester(582295-50-9)

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: 582295-50-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 582295-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,2,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 582295-50:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*5)+(2*5)+(1*0)=179
179 % 10 = 9
So 582295-50-9 is a valid CAS Registry Number.

582295-50-9Upstream product

582295-50-9Downstream Products

582295-50-9Relevant academic research and scientific papers

A highly selective route to beta-C-glycosides via nonselective samarium iodide induced coupling reactions.

Palmier, Sara,Vauzeilles, Boris,Beau, Jean-Marie

, p. 1097 - 1098 (2003)

Stereoselective preparation of beta-C-glycosides has been developed from acetylated glycopyranosyl 2-pyridyl sulfones, involving a samarium-Barbier coupling procedureoxidation-isomerization sequence.

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