Cas 1476029-40-9,(2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine

1476029-40-9

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Basic information

Product Name: (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine
Synonyms: (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine
CAS NO:1476029-40-9
Molecular Formula:
Molecular Weight: 645.796
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: (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine(1476029-40-9)
EPA Substance Registry System: (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine(1476029-40-9)

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: 1476029-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1476029-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,0,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1476029-40:
(9*1)+(8*4)+(7*7)+(6*6)+(5*0)+(4*2)+(3*9)+(2*4)+(1*0)=169
169 % 10 = 9
So 1476029-40-9 is a valid CAS Registry Number.

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1476029-40-9Relevant academic research and scientific papers

Copper-catalyzed synthesis of N-aryl-D-glucosamines from arylboronic acids

Tao, Chuanzhou,Liu, Feng,Xu, Bin,Cao, Zhiling,Wang, Huiyan,Liu, Weiwei

, p. 411 - 423 (2013/11/06)

A convenient catalytic protocol was developed to synthesize N-aryl-D-glucosamines from the corresponding arylboronic acids. CN cross-coupling between arylboronic acids and 1,3,4,6-tetra-O-benzyl-β-D- glucosamine was realized by copper catalyst under mild conditions. Subsequent deprotection of the benzyl ethers gave the N-arylation products, N-aryl-D-glucosamines.

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