Cas 1200396-66-2,4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside

1200396-66-2

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Basic information

Product Name: 4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside
Synonyms: 4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside
CAS NO:1200396-66-2
Molecular Formula:
Molecular Weight: 717.91
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: 4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside(1200396-66-2)
EPA Substance Registry System: 4-(pyridin-2-yl)thiazol-2-yl 2,3,4-tri-O-benzyl-6-O-picolyl-1-thio-β-D-glucopyranoside(1200396-66-2)

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: 1200396-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1200396-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,3,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1200396-66:
(9*1)+(8*2)+(7*0)+(6*0)+(5*3)+(4*9)+(3*6)+(2*6)+(1*6)=112
112 % 10 = 2
So 1200396-66-2 is a valid CAS Registry Number.

1200396-66-2Upstream product

1200396-66-2Downstream Products

1200396-66-2Relevant academic research and scientific papers

Coordination chemistry approach to the long-standing challenge of stereocontrolled chemical glycosylation

Pornsuriyasak, Papapida,Vetter, Cornelia,Kaeothip, Sophon,Kovermann, Michael,Balbach, Jochen,Steinborn, Dirk,Demchenko, Alexei V.

, p. 6379 - 6381 (2009)

This study clearly demonstrates that a multi-dentate metal coordination to the leaving group, along with O-5 and/or a protecting group at O-6, has a strong effect on the stereoselectivity of chemical glycosylation.

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