Cas 154774-31-9,benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside

154774-31-9

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Basic information

Product Name: benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside
Synonyms: benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside
CAS NO:154774-31-9
Molecular Formula:
Molecular Weight: 1535.53
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: benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside(154774-31-9)
EPA Substance Registry System: benzyl 2,3,4,6-tetrakis(3,4-((diphenylmethylene)dioxy)-5-hydroxybenzoyl)-β-D-glucopyranoside(154774-31-9)

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: 154774-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 154774-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,7,7 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 154774-31:
(8*1)+(7*5)+(6*4)+(5*7)+(4*7)+(3*4)+(2*3)+(1*1)=149
149 % 10 = 9
So 154774-31-9 is a valid CAS Registry Number.

154774-31-9Upstream product

154774-31-9Downstream Products

154774-31-9Relevant academic research and scientific papers

Ellagitannin chemistry. The first total chemical synthesis of an ellagitannin natural product, tellimagrandin I

Feldman, Ken S.,Ensel, Susan M.,Minard, Robert D.

, p. 1742 - 1745 (1994)

Tellimagrandin I was synthesized by two different biogenetically patterned routes. One route featured diastereoselective galloyl ester coupling between the O(4) and O(6) galloyl moieties in a glucose-derived substrate bearing additional protected galloyl

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