Cas 79991-78-9,((5R,8S,9R,10R)-9-Hydroxy-8-methoxy-2-oxo-1,7-dioxa-3-aza-spiro[4.5]dec-10-yl)-methyl-carbamic acid benzyl ester

79991-78-9

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Basic information

Product Name: ((5R,8S,9R,10R)-9-Hydroxy-8-methoxy-2-oxo-1,7-dioxa-3-aza-spiro[4.5]dec-10-yl)-methyl-carbamic acid benzyl ester
Synonyms:
CAS NO:79991-78-9
Molecular Formula:
Molecular Weight: 366.371
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: ((5R,8S,9R,10R)-9-Hydroxy-8-methoxy-2-oxo-1,7-dioxa-3-aza-spiro[4.5]dec-10-yl)-methyl-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((5R,8S,9R,10R)-9-Hydroxy-8-methoxy-2-oxo-1,7-dioxa-3-aza-spiro[4.5]dec-10-yl)-methyl-carbamic acid benzyl ester(79991-78-9)
EPA Substance Registry System: ((5R,8S,9R,10R)-9-Hydroxy-8-methoxy-2-oxo-1,7-dioxa-3-aza-spiro[4.5]dec-10-yl)-methyl-carbamic acid benzyl ester(79991-78-9)

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: 79991-78-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79991-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,9 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79991-78:
(7*7)+(6*9)+(5*9)+(4*9)+(3*1)+(2*7)+(1*8)=209
209 % 10 = 9
So 79991-78-9 is a valid CAS Registry Number.

79991-78-9Upstream product

79991-77-8 methyl 3-N-(benzyloxycarbonyl)-4-O-(azidocarbonyl)-β-garosaminide

79991-78-9Downstream Products

79991-78-9Relevant academic research and scientific papers

Acyl Nitrene Cyclisations in Antibiotics. Synthesis of 6''-Aminogentamicin C2

Wright, J. J. Kim,Albarella, James A.,Lee, Paul

, p. 523 - 527 (1982)

The insertion reaction of an acyl nitrene has been used to functionalize the branched-chain sugar moiety, garosamine, of the antibiotic gentamicin C2.Contrary to expectations based on intermolecular reactions in simple systems, insertion into the branched

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