Cas 1080487-98-4,1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene

1080487-98-4

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Basic information

Product Name: 1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene
Synonyms: 1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene
CAS NO:1080487-98-4
Molecular Formula:
Molecular Weight: 408.538
EINECS: N/A
Product Categories: N/A
Mol File: 1080487-98-4.mol
Article Data: 1

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: 1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene(CAS DataBase Reference)
NIST Chemistry Reference: 1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene(1080487-98-4)
EPA Substance Registry System: 1-[5-O-benzyl-2,3-O-(3-pentylidene)-β-D-ribofuranosyl]-2-propenylbenzene(1080487-98-4)

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: 1080487-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1080487-98-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,0,4,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1080487-98:
(9*1)+(8*0)+(7*8)+(6*0)+(5*4)+(4*8)+(3*7)+(2*9)+(1*8)=164
164 % 10 = 4
So 1080487-98-4 is a valid CAS Registry Number.

1080487-98-4Upstream product

1080487-98-4Downstream Products

1080487-98-4Relevant articles and documents

Highly β-selective C-allylation of a ribofuranoside controlling steric hindrance in the transition state

Ichikawa, Satoshi,Hayashi, Ryoko,Hirano, Shinpei,Matsuda, Akira

supporting information; experimental part, p. 5107 - 5110 (2009/05/30)

(Graph Presented) A highly β-selective C-allylation oi 2,3-O-(3-pentylidene)-D-ribofuranosyl fluoride is described. This strategy will provide a new concept for synthesizing β-C-ribosides by controlling the effect of steric hindrance in the transition state.

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