Cas 68267-29-8,(E)-1-Isoquinolin-1-yl-2,4-diphenyl-but-3-en-2-ol

68267-29-8

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Basic information

Product Name: (E)-1-Isoquinolin-1-yl-2,4-diphenyl-but-3-en-2-ol
Synonyms:
CAS NO:68267-29-8
Molecular Formula:
Molecular Weight: 351.448
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: (E)-1-Isoquinolin-1-yl-2,4-diphenyl-but-3-en-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-Isoquinolin-1-yl-2,4-diphenyl-but-3-en-2-ol(68267-29-8)
EPA Substance Registry System: (E)-1-Isoquinolin-1-yl-2,4-diphenyl-but-3-en-2-ol(68267-29-8)

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: 68267-29-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 68267-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,6 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68267-29:
(7*6)+(6*8)+(5*2)+(4*6)+(3*7)+(2*2)+(1*9)=158
158 % 10 = 8
So 68267-29-8 is a valid CAS Registry Number.

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68267-29-8Relevant academic research and scientific papers

LATERAL METALLATION OF METHYLATED NITROGENOUS HETEROCYCLES

Kaiser, Edwin M.

, p. 2055 - 2064 (2007/10/02)

Me groups on nitrogenous heterocycles can be conveniently metallated by a variety of strongly basic reagents to afford synthetically useful carbanions.The negative charge of such anions resides predominantly on the ring N atoms.The site of lithiation on pyridines and quinolines bearing Me groups in both the 2- and 4-positions depends upon the ability of the ring N atom to complex with the metallating agents.Carbanions derived from methylated pyridines, quinolines, naphthyridines, isoquinolines, pyridocarbazoles, pteridines, pyridoindoles and quinoxalines are discussed.References are provided describing condensations of these reagents with a variety of both common and uncommon electrophiles.

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