Cas 1107660-52-5,p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside

1107660-52-5

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Basic information

Product Name: p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
Synonyms: p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
CAS NO:1107660-52-5
Molecular Formula:
Molecular Weight: 481.483
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: p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside(1107660-52-5)
EPA Substance Registry System: p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside(1107660-52-5)

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: 1107660-52-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1107660-52-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,7,6,6 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1107660-52:
(9*1)+(8*1)+(7*0)+(6*7)+(5*6)+(4*6)+(3*0)+(2*5)+(1*2)=125
125 % 10 = 5
So 1107660-52-5 is a valid CAS Registry Number.

1107660-52-5Upstream product

36874-86-9 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-aminophenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate

1107660-52-5Downstream Products

1107660-52-5Relevant academic research and scientific papers

Thio-arylglycosides with various aglycon para-substituents: A probe for studying chemical glycosylation reactions

Li, Xiaoning,Huang, Lijun,Hu, Xiche,Huang, Xuefei

, p. 117 - 127 (2009)

Three series of thioglycosyl donors differing only in their respective aglycon substituents within each series have been prepared as representatives of typical glycosyl donors. The relative anomeric reactivities of these donors were quantified under compe

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