Cas 1610558-26-3,methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside

1610558-26-3

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Basic information

Product Name: methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside
Synonyms: methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside
CAS NO:1610558-26-3
Molecular Formula:
Molecular Weight: 457.553
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: methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside(1610558-26-3)
EPA Substance Registry System: methyl 6-(tert-butyldimethylsilyloxy)-2-O-(2-nitrobenzoyl)-α-D-glucopyranoside(1610558-26-3)

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: 1610558-26-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1610558-26-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,5,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1610558-26:
(9*1)+(8*6)+(7*1)+(6*0)+(5*5)+(4*5)+(3*8)+(2*2)+(1*6)=143
143 % 10 = 3
So 1610558-26-3 is a valid CAS Registry Number.

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1610558-26-3Relevant academic research and scientific papers

Recognition and site-selective transformation of monosaccharides by using copper(II) catalysis

Chen, I-Hon,Kou, Kevin G. M.,Le, Diane N.,Rathbun, Colin M.,Dong, Vy M.

supporting information, p. 5013 - 5018 (2014/05/06)

We demonstrate copper(II)-catalyzed acylation and tosylation of monosaccharides. Various carbohydrate derivatives, including glucopyranosides and ribofuranosides, are obtained in high yields and regioselectivities. Using this versatile strategy, the site

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