Cas 286466-53-3,Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane

286466-53-3

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Basic information

Product Name: Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane
Synonyms: Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane
CAS NO:286466-53-3
Molecular Formula:
Molecular Weight: 1161.47
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: Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane(CAS DataBase Reference)
NIST Chemistry Reference: Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane(286466-53-3)
EPA Substance Registry System: Diphenyl-bis-[(S)-1-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-allyloxy]-silane(286466-53-3)

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: 286466-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 286466-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,4,6 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 286466-53:
(8*2)+(7*8)+(6*6)+(5*4)+(4*6)+(3*6)+(2*5)+(1*3)=183
183 % 10 = 3
So 286466-53-3 is a valid CAS Registry Number.

286466-53-3Upstream product

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286466-53-3Relevant academic research and scientific papers

Ring-closing metathesis as a new strategy for the C-C coupling of monosaccharide derivatives via silicon tethering

Lobbel, Michael,Koell, Peter

, p. 393 - 396 (2007/10/03)

Suitable carbohydrate-derived terminal olefins have been coupled by ring-closing metathesis reaction following a silicon tethering strategy, generating very long contiguous chains of carbon atoms each equipped with specific stereochemistry and functionali

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