Cas 1053260-72-2,(2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester

1053260-72-2

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Basic information

Product Name: (2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
Synonyms: (2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
CAS NO:1053260-72-2
Molecular Formula:
Molecular Weight: 736.947
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: (2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester(1053260-72-2)
EPA Substance Registry System: (2S,4S,5R,6R)-5-Azido-6-[(1S,2R)-1,2-bis-(4-chloro-benzoyloxy)-3-hydroxy-propyl]-4-(4-chloro-benzoyloxy)-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester(1053260-72-2)

Safety Data

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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1053260-72-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1053260-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,3,2,6 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1053260-72:
(9*1)+(8*0)+(7*5)+(6*3)+(5*2)+(4*6)+(3*0)+(2*7)+(1*2)=112
112 % 10 = 2
So 1053260-72-2 is a valid CAS Registry Number.

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1053260-72-2Relevant academic research and scientific papers

The thioglycoside and glycosyl phosphite of 5-Azido sialic acid: Excellent donors for the α-glycosylation of primary hydroxy groups

Yu, Chung-Shan,Niikura, Kenichi,Lin, Chun-Cheng,Wong, Chi-Huey

, p. 2900 - 2903 (2007/10/03)

5-Azido sialyl donors with O-acetyl protecting groups are useful α-selective glycosylation reagents, especially for primary hydroxyl groups as acceptors. This is shown with a variety of reactions using 1 as a sialyl donor. It was also possible to synthesi

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