Cas 881198-69-2,1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose

881198-69-2

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Basic information

Product Name: 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose
Synonyms: 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose
CAS NO:881198-69-2
Molecular Formula:
Molecular Weight: 879.016
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: 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose(881198-69-2)
EPA Substance Registry System: 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose(881198-69-2)

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: 881198-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 881198-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,1,9 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 881198-69:
(8*8)+(7*8)+(6*1)+(5*1)+(4*9)+(3*8)+(2*6)+(1*9)=212
212 % 10 = 2
So 881198-69-2 is a valid CAS Registry Number.

881198-69-2Upstream product

881198-69-2Downstream Products

881198-69-2Relevant academic research and scientific papers

2-Allylphenyl glycosides as glycosyl donors for sugar coupling

Luo, Shun-Yuan,Tripathi, Ashish,Zulueta, Medel Manuel L.,Hung, Shang-Cheng

, p. 197 - 201 (2012/06/30)

Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins.

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