Cas 290820-11-0,(E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol

290820-11-0

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Basic information

Product Name: (E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol
Synonyms: (E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol
CAS NO:290820-11-0
Molecular Formula:
Molecular Weight: 490.596
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: (E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol(290820-11-0)
EPA Substance Registry System: (E)-(R)-4-Benzyloxy-4-((2S,3S,4R,5R)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-but-2-en-1-ol(290820-11-0)

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: 290820-11-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 290820-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,8,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 290820-11:
(8*2)+(7*9)+(6*0)+(5*8)+(4*2)+(3*0)+(2*1)+(1*1)=130
130 % 10 = 0
So 290820-11-0 is a valid CAS Registry Number.

290820-11-0Upstream product

127501-24-0 methyl 2,3,5-tri-O-benzyl-β-D-galactofuranoside

290820-11-0Downstream Products

290820-17-6 methyl 2,3-di-O-benzyl-5,6,7,8-tetradeoxy-β-L-arabino-oct-5(E),7-dieno-1,4-furanoside

290820-11-0Relevant academic research and scientific papers

A convenient route to enantiomerically pure, conjugated dienes from sugar allyltin derivatives

Jarosz, Slawomir,Skora, Stanislaw,Szewczyk, Katarzyna

, p. 1997 - 2006 (2007/10/03)

The transformation of sugar allyltin derivatives into enantiomerically pure dienes (R*-CH=CH-CH=CH2) is presented. The internal double bond with the trans-configuration is formed regardless of the configuration of the starting sugar allyltin. Copyright (C) 2000 Elsevier Science Ltd.

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