84029-69-6 Usage
Compound type
Polycyclic aromatic hydrocarbon (PAH)
Structure
Naphthalene ring with a tert-butyl group at the 2-position and a methyl group at the 6-position
Uses
Production of dyes, solvent, intermediate in organic synthesis
Safety concerns
Potential mutagenic and carcinogenic properties, proper safety precautions should be taken when handling and using.
Check Digit Verification of cas no
The CAS Registry Mumber 84029-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84029-69:
(7*8)+(6*4)+(5*0)+(4*2)+(3*9)+(2*6)+(1*9)=136
136 % 10 = 6
So 84029-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H18/c1-11-5-6-13-10-14(15(2,3)4)8-7-12(13)9-11/h5-10H,1-4H3
84029-69-6Relevant academic research and scientific papers
Electron Paramagnetic Resonance Spectra of Substituted 1- and 2-Naphthylmethyl Radicals
Jackson, Richard A.,Rhodes, Christopher J.
, p. 53 - 57 (2007/10/02)
The EPR spectra of 7-tert-butyl-1-naphthylmethyl and 6-tert-butyl-2-naphthylmethyl radicals, prepared by photolysis of the hydrocarbon with tert-butyl peroxide at -40 deg C, have been analysed by correlation methods: average α(C-H) coupling constants are 15.0 and 15.25 G respectively, in line with the expected relative stabilities of the two radicals and the recently reported stabilization energy for 1-naphthylmethyl.
