Cas 1075217-33-2,methyl 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside

1075217-33-2

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Basic information

Product Name: methyl 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside
Synonyms: methyl 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside
CAS NO:1075217-33-2
Molecular Formula:
Molecular Weight: 526.586
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 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside(1075217-33-2)
EPA Substance Registry System: methyl 2-O-benzoyl-3-O-benzyl-4,6-O-(1-naphthylmethylidene)-α-L-idopyranoside(1075217-33-2)

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: 1075217-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1075217-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,2,1 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1075217-33:
(9*1)+(8*0)+(7*7)+(6*5)+(5*2)+(4*1)+(3*7)+(2*3)+(1*3)=132
132 % 10 = 2
So 1075217-33-2 is a valid CAS Registry Number.

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1075217-33-2Relevant academic research and scientific papers

Synthesis of the putative minimal FGF binding motif heparan sulfate trisaccharides by an orthogonal protecting group strategy

Tatai, János,Fügedi, Péter

experimental part, p. 9865 - 9873 (2009/04/03)

The synthesis of two trisaccharides, the putative minimal heparan sulfate sequences responsible for binding to acidic and basic fibroblast growth factors, respectively, is described from a common protected intermediate using an orthogonal protecting group strategy.

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