Cas 1314535-68-6,6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile

1314535-68-6

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Basic information

Product Name: 6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile
Synonyms: 6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile
CAS NO:1314535-68-6
Molecular Formula:
Molecular Weight: 329.445
EINECS: N/A
Product Categories: N/A
Mol File: 1314535-68-6.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: 6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile(1314535-68-6)
EPA Substance Registry System: 6-tert-butyl-1-methyl-3-phenyl-2,3-dihydroquinoline-4,4(1H)-dicarbonitrile(1314535-68-6)

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: 1314535-68-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314535-68-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,5,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1314535-68:
(9*1)+(8*3)+(7*1)+(6*4)+(5*5)+(4*3)+(3*5)+(2*6)+(1*8)=136
136 % 10 = 6
So 1314535-68-6 is a valid CAS Registry Number.

1314535-68-6Upstream product

1314535-68-6Downstream Products

1314535-68-6Relevant articles and documents

Copper-catalyzed oxidative direct cyclization of N-methylanilines with electron-deficient alkenes using molecular oxygen

Nishino, Mayuko,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

experimental part, p. 6447 - 6451 (2011/09/15)

The oxidative direct cyclizaion of N-methylanilines with electron-deficient alkenes involving maleimides and benzylidene malononitriles through sp 3 and sp2 C-H bond cleavage proceeds effectively under a CuCl2/O2/sub

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