Cas 100324-89-8,N-(Benzyloxycarbonyl)-L-leucyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-galactopyranosyl)-L-serin-benzylester

100324-89-8

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Basic information

Product Name: N-(Benzyloxycarbonyl)-L-leucyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-galactopyranosyl)-L-serin-benzylester
Synonyms:
CAS NO:100324-89-8
Molecular Formula:
Molecular Weight: 771.819
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-(Benzyloxycarbonyl)-L-leucyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-galactopyranosyl)-L-serin-benzylester(CAS DataBase Reference)
NIST Chemistry Reference: N-(Benzyloxycarbonyl)-L-leucyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-galactopyranosyl)-L-serin-benzylester(100324-89-8)
EPA Substance Registry System: N-(Benzyloxycarbonyl)-L-leucyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-galactopyranosyl)-L-serin-benzylester(100324-89-8)

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: 100324-89-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100324-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100324-89:
(8*1)+(7*0)+(6*0)+(5*3)+(4*2)+(3*4)+(2*8)+(1*9)=68
68 % 10 = 8
So 100324-89-8 is a valid CAS Registry Number.

100324-89-8Upstream product

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100324-89-8Relevant academic research and scientific papers

Building Units of Oligosaccharides, LXVI. - Synthesis of O-Glycopeptide Blocks of Glycophorine

Paulsen, Hans,Schultz, Michael,Klamann, Joerg-Dieter,Waller, Birgit,Paal, Michael

, p. 2028 - 2048 (2007/10/02)

A block synthesis to O-glycopeptides can be realized by reaction of the disaccharide halide 10 with either L-serine- or L-threonine-containing peptide derivatives.Thus, the reaction of 10 with 8 yields stereoselectively the L-Ser-L-Ser derivative 15 in wh

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