Cas 500894-20-2,((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol

500894-20-2

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Basic information

Product Name: ((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol
Synonyms: ((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol
CAS NO:500894-20-2
Molecular Formula:
Molecular Weight: 404.506
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: ((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol(500894-20-2)
EPA Substance Registry System: ((2R,3R,4R,5S)-5-Benzyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol(500894-20-2)

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: 500894-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 500894-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,8,9 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 500894-20:
(8*5)+(7*0)+(6*0)+(5*8)+(4*9)+(3*4)+(2*2)+(1*0)=132
132 % 10 = 2
So 500894-20-2 is a valid CAS Registry Number.

500894-20-2Upstream product

500894-20-2Downstream Products

500894-21-3 (2S,3S,4S,5R)-2-Benzyl-5-hydroxymethyl-tetrahydro-furan-3,4-diol

500894-20-2Relevant academic research and scientific papers

Efficient access to ATP mimics, potential FGF receptor tyrosine kinase inhibitors

Rigolet, Séverinne,McCort, Isabelle,Le Merrer, Yves

, p. 8129 - 8132 (2002)

Nucleophilic opening of bis-epoxide 1 derived from D-mannitol by organolithium species in the presence of boron trifluoride etherate allows the synthesis of enantiopure polyhydroxy tetrahydrofurane skeletons with aromatic moieties in the pseudo-anomeric p

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