Cas 923036-86-6,[1-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine

923036-86-6

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Basic information

Product Name: [1-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine
Synonyms: [1-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine
CAS NO:923036-86-6
Molecular Formula:
Molecular Weight: 300.403
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-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(CAS DataBase Reference)
NIST Chemistry Reference: [1-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(923036-86-6)
EPA Substance Registry System: [1-(6-Methyl-pyridin-2-yl)-1-phenyl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(923036-86-6)

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: 923036-86-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 923036-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,3 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 923036-86:
(8*9)+(7*2)+(6*3)+(5*0)+(4*3)+(3*6)+(2*8)+(1*6)=156
156 % 10 = 6
So 923036-86-6 is a valid CAS Registry Number.

923036-86-6Upstream product

923036-86-6Downstream Products

923036-86-6Relevant academic research and scientific papers

Synthesis of optically active imidazopyridinium salts and the corresponding NHCs

Schmidt, Michael A.,Movassaghi, Mohammad

, p. 101 - 104 (2007)

A convergent synthesis of chiral imidazo-[1,5-a]-pyridinium salts is described by facile introduction of a stereogenic center via the N2 substituent. Conversion of these optically active salts to the corresponding N-heterocyclic carbenes (NHCs) and their trapping with sulfur followed by optical activity measurements are discussed.

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