Cas 79635-34-0,((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester

79635-34-0

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Basic information

Product Name: ((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester
Synonyms: ((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester
CAS NO:79635-34-0
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: ((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester(79635-34-0)
EPA Substance Registry System: ((4R,5S,7R)-5,7-Dihydroxy-4-methoxy-3-methyl-2-oxo-octahydro-benzooxazol-6-yl)-carbamic acid benzyl ester(79635-34-0)

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: 79635-34-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79635-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79635-34:
(7*7)+(6*9)+(5*6)+(4*3)+(3*5)+(2*3)+(1*4)=170
170 % 10 = 0
So 79635-34-0 is a valid CAS Registry Number.

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79635-34-0Relevant academic research and scientific papers

Synthesis of (-)-Fortamine and (+)-2-Deoxyfortamine From Resolved 3S,4S-Carbomethoxy-3-aminocyclohexen-4-ol

Knapp, Spencer,Sebastian, Mark J.,Ramanathan, Halasya,Bharadwaj, Parimal,Potenza, Joseph A.

, p. 3405 - 3410 (2007/10/02)

A three step sequence (Scheme I) starting with racemic 3,4-epoxycyclohexene (5) and (S)-α-methylbenzylamine gave 3S,4S-N-carbomethoxy-3-aminocyclohexen-4-ol (10) with chromatographic removal of the undesired 3R,4R byproduct.The absolute configuration of 1

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