Cas 1052658-52-2,(R)-5-{(S)-Benzyloxy-[(2S,3S)-3-(tert-butyl-dimethyl-silanyloxy)-5-iodomethyl-tetrahydro-furan-2-yl]-methyl}-2,2-dimethyl-[1,3]dioxolan-4-ol

1052658-52-2

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Basic information

Product Name: (R)-5-{(S)-Benzyloxy-[(2S,3S)-3-(tert-butyl-dimethyl-silanyloxy)-5-iodomethyl-tetrahydro-furan-2-yl]-methyl}-2,2-dimethyl-[1,3]dioxolan-4-ol
Synonyms:
CAS NO:1052658-52-2
Molecular Formula:
Molecular Weight: 578.56
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: (R)-5-{(S)-Benzyloxy-[(2S,3S)-3-(tert-butyl-dimethyl-silanyloxy)-5-iodomethyl-tetrahydro-furan-2-yl]-methyl}-2,2-dimethyl-[1,3]dioxolan-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-{(S)-Benzyloxy-[(2S,3S)-3-(tert-butyl-dimethyl-silanyloxy)-5-iodomethyl-tetrahydro-furan-2-yl]-methyl}-2,2-dimethyl-[1,3]dioxolan-4-ol(1052658-52-2)
EPA Substance Registry System: (R)-5-{(S)-Benzyloxy-[(2S,3S)-3-(tert-butyl-dimethyl-silanyloxy)-5-iodomethyl-tetrahydro-furan-2-yl]-methyl}-2,2-dimethyl-[1,3]dioxolan-4-ol(1052658-52-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1052658-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1052658-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,2,6,5 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1052658-52:
(9*1)+(8*0)+(7*5)+(6*2)+(5*6)+(4*5)+(3*8)+(2*5)+(1*2)=142
142 % 10 = 2
So 1052658-52-2 is a valid CAS Registry Number.

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1052658-52-2Relevant academic research and scientific papers

1,2-O-Isopropylidenefuranose Templates for the Synthesis of Complex Cyclic Ethers via Neighboring Group Participation by the Acetal Ring Oxygen

Shan, Weifang,Wilson, Phyllis,Liang, Wei,Mootoo, David R.

, p. 7986 - 7993 (2007/10/02)

Novel strategies are described for the direct transformation of C5-allylated-1,2-O-isopropylidene-furanoses into complex cyclic ethers.Reaction of these substrates with iodonium ion under aqueous conditions resulted in the facile formation of 2,5-disubsti

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