Cas 857468-85-0,(1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate

857468-85-0

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Basic information

Product Name: (1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate
Synonyms: (1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate
CAS NO:857468-85-0
Molecular Formula:
Molecular Weight: 770.83
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: (1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate(857468-85-0)
EPA Substance Registry System: (1R,2S,3S,4R)-1-(5,7-bis(benzyloxy)-1,3-dihydro-1-methoxyisobenzofuran-1-yl)-5-(benzyloxy)pentane-1,2,3,4-tetraacetate(857468-85-0)

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: 857468-85-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 857468-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,4,6 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 857468-85:
(8*8)+(7*5)+(6*7)+(5*4)+(4*6)+(3*8)+(2*8)+(1*5)=230
230 % 10 = 0
So 857468-85-0 is a valid CAS Registry Number.

857468-85-0Upstream product

857468-85-0Downstream Products

857468-85-0Relevant academic research and scientific papers

De novo synthesis of a galacto-papulacandin moiety via an iterative dihydroxylation strategy

Ahmed, Md. Moinuddin,O'Doherty, George A.

, p. 4151 - 4155 (2007/10/03)

A short and highly efficient route to both the pyranose and furanose forms of a galacto-papulacandin ring system has been developed. The key to the overall transformation is the sequential two osmium-catalyzed dihydroxylation reactions of substituted 2,4-

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