Cas 1260495-19-9,1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol

1260495-19-9

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Basic information

Product Name: 1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol
Synonyms: 1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol
CAS NO:1260495-19-9
Molecular Formula:
Molecular Weight: 303.361
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: 1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol(1260495-19-9)
EPA Substance Registry System: 1-(4-phenyl-1H-1,2,3-triazol-1-yl)-3-(tetrahydro-2H-pyran-2-yloxy)-propan-2-ol(1260495-19-9)

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: 1260495-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260495-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,4,9 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1260495-19:
(9*1)+(8*2)+(7*6)+(6*0)+(5*4)+(4*9)+(3*5)+(2*1)+(1*9)=149
149 % 10 = 9
So 1260495-19-9 is a valid CAS Registry Number.

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1260495-19-9Relevant academic research and scientific papers

Zeo-click chemistry: Copper(I)-zeolite-catalyzed cascade reaction; One-pot epoxide ring-opening and cycloaddition

Boningari, Thirupathi,Olmos, Andrea,Reddy, Benjaram M.,Sommer, Jean,Pale, Patrick

experimental part, p. 6338 - 6347 (2011/03/17)

Copper(I)-modified zeolites, especially CuI-USY, proved to be very efficient catalysts in multi-component reactions of epoxides with sodium azide and terminal alkynes. Such catalysts allow highly regio- and stereoselective syntheses ofhydroxyme

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