Cas 365535-22-4,methyl (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

365535-22-4

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Basic information

Product Name: methyl (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
Synonyms: methyl (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
CAS NO:365535-22-4
Molecular Formula:
Molecular Weight: 796.912
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 (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside(365535-22-4)
EPA Substance Registry System: methyl (3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside(365535-22-4)

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: 365535-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 365535-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,5,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 365535-22:
(8*3)+(7*6)+(6*5)+(5*5)+(4*3)+(3*5)+(2*2)+(1*2)=154
154 % 10 = 4
So 365535-22-4 is a valid CAS Registry Number.

365535-22-4Upstream product

365535-22-4Downstream Products

192936-03-1 methyl O-(3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

365535-22-4Relevant academic research and scientific papers

2-(Hydroxycarbonyl)benzyl glycosides: A novel type of glycosyl donors for highly efficient β-mannopyranosylation and oligosaccharide synthesis by latent-active glycosylation

Kwan Soo Kim,Jin Hwan Kim,Yong Joo Lee,Yong Jun Lee,Park

, p. 8477 - 8481 (2001)

2-(Benzyloxycarbonyl)benzyl (BCB) glycosides were prepared by coupling of the corresponding tetraacetylglycosyl bromides and benzyl 2-(hydroxymethyl)benzoate. The BCB glycosides were converted almost quantitatively into the corresponding 2-(hydroxycarbony

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