Cas 1449522-19-3,(S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride

1449522-19-3

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Basic information

Product Name: (S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride
Synonyms: (S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride
CAS NO:1449522-19-3
Molecular Formula:
Molecular Weight: 335.877
EINECS: N/A
Product Categories: N/A
Mol File: 1449522-19-3.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: (S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride(CAS DataBase Reference)
NIST Chemistry Reference: (S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride(1449522-19-3)
EPA Substance Registry System: (S)-5-sec-butyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride(1449522-19-3)

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: 1449522-19-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449522-19-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,5,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1449522-19:
(9*1)+(8*4)+(7*4)+(6*9)+(5*5)+(4*2)+(3*2)+(2*1)+(1*9)=173
173 % 10 = 3
So 1449522-19-3 is a valid CAS Registry Number.

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1449522-19-3Relevant articles and documents

Testing new ruthenium complexes bearing chiral 1,2,4-triazol-5-ylidene- ligands as catalysts for asymmetric olefin metathesis

Gawin, Rafa?,Pieczykolan, Micha?,Malińska, Maura,Wo?niak, Krzysztof,Grela, Karol

, p. 1250 - 1254 (2013)

New ruthenium complexes bearing chiral 1,2,4-triazol-5-ylidene ligands were obtained and tested in model asymmetric metathesis reactions. Low enantioselectivity in asymmetric ring-closing metathesis (ARCM) and moderate enantioselectivity in asymmetric rin

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