Cas 1619941-84-2,3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside

1619941-84-2

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Basic information

Product Name: 3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside
Synonyms: 3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside
CAS NO:1619941-84-2
Molecular Formula:
Molecular Weight: 320.342
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: 3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside(1619941-84-2)
EPA Substance Registry System: 3-methylphenyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside(1619941-84-2)

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: 1619941-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1619941-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,9,9,4 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1619941-84:
(9*1)+(8*6)+(7*1)+(6*9)+(5*9)+(4*4)+(3*1)+(2*8)+(1*4)=202
202 % 10 = 2
So 1619941-84-2 is a valid CAS Registry Number.

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1619941-84-2Relevant academic research and scientific papers

ZnBr2-catalyzed and microwave-assisted synthesis of 2,3-unsaturated glucosides of hindered phenols and alcohols

Bound, D. James,Bettadaiah,Srinivas

, p. 2565 - 2576 (2014/08/05)

GRAPHICAL ABSTRACT Zinc bromide (ZnBr2) under microwave irradiation efficiently catalyzed the Ferrier reaction of hindered phenols and alcohols to afford the corresponding α-2,3-unsaturated glucoside acetates in good yields and with good stereoselectivity. The reaction affords a facile access to new 2,3-dideoxyglucosides of important phenolic and alcoholic constituents of spices.

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