Cas 164664-79-3,methyl O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside

164664-79-3

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Basic information

Product Name: methyl O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside
Synonyms: methyl O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside
CAS NO:164664-79-3
Molecular Formula:
Molecular Weight: 754.831
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 O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside(164664-79-3)
EPA Substance Registry System: methyl O-(6-O-acetyl-3-O-benzoyl-4-O-α-D-arabino-hexopyranosyl)-(1<*>6)-3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexapyranoside(164664-79-3)

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: 164664-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 164664-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,6,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 164664-79:
(8*1)+(7*6)+(6*4)+(5*6)+(4*6)+(3*4)+(2*7)+(1*9)=163
163 % 10 = 3
So 164664-79-3 is a valid CAS Registry Number.

164664-79-3Upstream product

164664-79-3Downstream Products

164664-79-3Relevant academic research and scientific papers

Synthesis of methyl glycosides of some α-isomalto oligosaccharides specifically deoxygenated at position C-2

Petrakova,Glaudemans

, p. 35 - 46 (2007/10/02)

Methyl α-isomaltoside and methyl α-isomaltotrioside analogues specifically deoxygenated at position C-2 of various glucopyranosyl units were synthesized by condensation of either 6-O-acetyl-3-O-benzoyl-4-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy- β-D-a

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