Cas 676349-29-4,2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane

676349-29-4

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Basic information

Product Name: 2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane
Synonyms: 2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane
CAS NO:676349-29-4
Molecular Formula:
Molecular Weight: 510.819
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: 2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane(676349-29-4)
EPA Substance Registry System: 2-[(2R,3R,4S,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenoxy-tetrahydro-furan-2-yl]-2-methyl-[1,3]dioxolane(676349-29-4)

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: 676349-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 676349-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,3,4 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 676349-29:
(8*6)+(7*7)+(6*6)+(5*3)+(4*4)+(3*9)+(2*2)+(1*9)=204
204 % 10 = 4
So 676349-29-4 is a valid CAS Registry Number.

676349-29-4Upstream product

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676349-29-4Relevant academic research and scientific papers

Furanose Synthesis via Regioselective Dihydroxylation of 1-Silyloxy-1,3-dienes: Application to the Furanose Unit of 4-epi-Hygromycin A

Armstrong, Alan,Gethin, David M.,Wheelhouse, Christopher J.

, p. 350 - 352 (2007/10/03)

Asymmetric dihydroxylation of a 1-silyloxy-1,3-diene is shown to occur regioselectively on the non-oxygenated alkene. Second dihydroxylation is complicated by over-oxidation to the dione and epimerisation of reaction products. However, subsequent manipula

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