Cas 133157-07-0,N-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester

133157-07-0

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Basic information

Product Name: N-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester
Synonyms: N-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester
CAS NO:133157-07-0
Molecular Formula:
Molecular Weight: 972.951
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-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester(133157-07-0)
EPA Substance Registry System: N-(diphenylmethylene)-O-(2,3,6,2',3',4',6'-hepta-O-acetyl-β-D-lactosyl)-(1<*>3)-L-seryl-L-glycine ethyl ester(133157-07-0)

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: 133157-07-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133157-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133157-07:
(8*1)+(7*3)+(6*3)+(5*1)+(4*5)+(3*7)+(2*0)+(1*7)=100
100 % 10 = 0
So 133157-07-0 is a valid CAS Registry Number.

133157-07-0Upstream product

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133157-07-0Relevant academic research and scientific papers

O-Glycopeptides: A simple β-stereoselective glycosidation of serine and threonine via a favorable hydrogen bonding pattern

Szabo,Li,Polt

, p. 585 - 588 (1991)

Glycosidation of serine and threonine is promoted by using an intramolecular hydrogen bond to the hydroxyl group.

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