Cas 227751-10-2,3',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate

227751-10-2

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Product Name: 3',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate
Synonyms: 3',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate
CAS NO:227751-10-2
Molecular Formula:
Molecular Weight: 900.839
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',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate(CAS DataBase Reference)
NIST Chemistry Reference: 3',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate(227751-10-2)
EPA Substance Registry System: 3',6'-di-O-acetyl-4'-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranose 1',2'-(methyl 4,6-O-benzylidene-α-D-glucopyranosid-3-yl) orthoacetate(227751-10-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 227751-10-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 227751-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,7,5 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 227751-10:
(8*2)+(7*2)+(6*7)+(5*7)+(4*5)+(3*1)+(2*1)+(1*0)=132
132 % 10 = 2
So 227751-10-2 is a valid CAS Registry Number.

227751-10-2Upstream product

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227751-10-2Relevant academic research and scientific papers

Regio- and stereoselective synthesis of oligosaccharides with acetobromolactose and acetobromomaltose as glycosyl donors via orthoester intermediates

Wang, Wei,Kong, Fanzuo

, p. 451 - 460 (1999)

Regio- and stereoselective synthesis of some trisaccharides was effected in high yields from coupling of acetobromolactose or acetobromomaltose as donors with partially protected glucoside acceptors through an orthoester formation-rearrangement strategy. Selective 1→6 or 1→3 with 1,2-trans glycosylation was achieved.

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