Cas 1434057-31-4,1-(4-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate

1434057-31-4

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Basic information

Product Name: 1-(4-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate
Synonyms: 1-(4-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate
CAS NO:1434057-31-4
Molecular Formula:
Molecular Weight: 366.123
EINECS: N/A
Product Categories: N/A
Mol File: 1434057-31-4.mol
Article Data: 2

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-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(1434057-31-4)
EPA Substance Registry System: 1-(4-(methoxycarbonyl)phenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(1434057-31-4)

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: 1434057-31-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1434057-31-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,4,0,5 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1434057-31:
(9*1)+(8*4)+(7*3)+(6*4)+(5*0)+(4*5)+(3*7)+(2*3)+(1*1)=134
134 % 10 = 4
So 1434057-31-4 is a valid CAS Registry Number.

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1434057-31-4Relevant articles and documents

Synthesis of unsymmetrical imidazolium salts by direct quaternization of N-substituted imidazoles using arylboronic acids

Li, Shiqing,Yang, Fan,Lv, Taiyong,Lan, Jingbo,Gao, Ge,You, Jingsong

, p. 3941 - 3943 (2014/04/03)

Imidazolium salts were conveniently prepared by direct aryl quaternization using arylboronic acids. This process features the tolerance of a broad range of functional groups and excellent chemoselectivity, and is especially effective for the synthesis of unsymmetrical imidazolium salts.

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