Cas 915404-08-9,methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside

915404-08-9

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Basic information

Product Name: methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside
Synonyms: methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside
CAS NO:915404-08-9
Molecular Formula:
Molecular Weight: 544.601
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: methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside(915404-08-9)
EPA Substance Registry System: methyl 2,4-di-O-(E)-cinnamoyl-3-O-p-methoxybenzyl-β-D-xylopyranoside(915404-08-9)

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: 915404-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915404-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,4,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 915404-08:
(8*9)+(7*1)+(6*5)+(5*4)+(4*0)+(3*4)+(2*0)+(1*8)=149
149 % 10 = 9
So 915404-08-9 is a valid CAS Registry Number.

915404-08-9Upstream product

915404-08-9Downstream Products

915404-09-0 methyl 2,4-di-O-(E)-cinnamoyl-β-D-xylopyranoside

915404-08-9Relevant academic research and scientific papers

Exploitation of sugar ring flipping for a hinge-type tether assisting a [2 + 2] cycloaddition

Yuasa, Hideya,Nakatani, Masatoshi,Hashimoto, Hironobu

, p. 3694 - 3702 (2008/10/09)

Methyl 3-O-p-methoxybenzyl-β-d-xylopyranoside (2) was exploited as a novel hinge-type tether for the [2 + 2] cycloaddition of cinnamate. The major ring conformation occupied by the 2,4-dicinnamate derivative of 2 was 4C1, which exten

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