Cas 1174411-22-3,N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine

1174411-22-3

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Basic information

Product Name: N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine
Synonyms: N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine
CAS NO:1174411-22-3
Molecular Formula:
Molecular Weight: 1027.94
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: N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine(CAS DataBase Reference)
NIST Chemistry Reference: N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine(1174411-22-3)
EPA Substance Registry System: N-(N-benzyloxycarbonyldiglycyl)-N-di{N-[4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]carbamoylmethyl}amine(1174411-22-3)

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: 1174411-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174411-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,4,1 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1174411-22:
(9*1)+(8*1)+(7*7)+(6*4)+(5*4)+(4*1)+(3*1)+(2*2)+(1*2)=123
123 % 10 = 3
So 1174411-22-3 is a valid CAS Registry Number.

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1174411-22-3Relevant academic research and scientific papers

Synthesis of bi- and tervalent ligands of galectins, derivatives of β-lactosylamine, with the amino group in the terminal position of the spacer

Likhosherstov,Novikova,Mokrov

, p. 660 - 664 (2008)

A method for the synthesis of glycoclusters by N-alkylation of N-glycyl-β-lactosylamine with N-chloroacetyl derivatives of β-lactosylamine and N,N'-iminodiacetyldilactosylamine has been developed. The glycoclusters obtained with two and three lactosylamine residues with the amino group in the spacer were found to be suitable for further conjugation with carboxy-containing physiologically active compounds.

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