Cas 1260495-17-7,2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate

1260495-17-7

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Basic information

Product Name: 2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate
Synonyms: 2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate
CAS NO:1260495-17-7
Molecular Formula:
Molecular Weight: 261.28
EINECS: N/A
Product Categories: N/A
Mol File: 1260495-17-7.mol
Article Data: 1

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: 2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate(CAS DataBase Reference)
NIST Chemistry Reference: 2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate(1260495-17-7)
EPA Substance Registry System: 2-hydroxy-3-(4-phenyl-1H-1,2,3-triazol-1-yl)propyl acetate(1260495-17-7)

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: 1260495-17-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260495-17-7 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 1260495-17:
(9*1)+(8*2)+(7*6)+(6*0)+(5*4)+(4*9)+(3*5)+(2*1)+(1*7)=147
147 % 10 = 7
So 1260495-17-7 is a valid CAS Registry Number.

1260495-17-7Upstream product

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1260495-17-7Relevant articles and documents

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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