Cas 823819-67-6,ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside

823819-67-6

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Basic information

Product Name: ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside
Synonyms: ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside
CAS NO:823819-67-6
Molecular Formula:
Molecular Weight: 528.667
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: ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside(823819-67-6)
EPA Substance Registry System: ethyl 2,6,-di-O-(2,6-dimethylbenzoyl)-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside(823819-67-6)

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: 823819-67-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 823819-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,8,1 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 823819-67:
(8*8)+(7*2)+(6*3)+(5*8)+(4*1)+(3*9)+(2*6)+(1*7)=186
186 % 10 = 6
So 823819-67-6 is a valid CAS Registry Number.

823819-67-6Upstream product

823819-67-6Downstream Products

823819-67-6Relevant academic research and scientific papers

Is acyl migration to the aglycon avoidable in 2-acyl assisted glycosylation reactions?

Berces, Attila,Whitfield, Dennis M.,Nukada, Tomoo,Do Santos Z, Iwona,Obuchowska, Agnes,Krepinsky, Jiri J.

, p. 1157 - 1171 (2004)

This report unequivocally separates orthoester formation from acyl transfer for the first time and indicates possible routes to eliminate 2-O-acyl transfer during glycosylation reactions. Experimental evidence is shown that acyl transfer from 2-O-acyl-3,4

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