84029-67-4 Usage
Type of compound
Polycyclic aromatic hydrocarbon
Structure
Contains multiple fused aromatic rings
Functional groups
tert-butyl group and methyl group
tert-butyl group
A branched alkyl group attached to the naphthalene ring
Methyl group
Attached to the naphthalene ring at a different position
Usage
Starting material in the synthesis of various organic compounds
Potential
As a ligand in coordination chemistry
Applications
Industrial applications and research tool in organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 84029-67-4 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 84029-67:
(7*8)+(6*4)+(5*0)+(4*2)+(3*9)+(2*6)+(1*7)=134
134 % 10 = 4
So 84029-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H18/c1-11-9-12-7-5-6-8-13(12)14(10-11)15(2,3)4/h5-10H,1-4H3
84029-67-4Relevant academic research and scientific papers
Type 1 ring-opening reactions of cyclopropanated 7-oxabenzonorbornadienes with organocuprates
Carlson, Emily,Haner, Jamie,McKee, Mary,Tam, William
supporting information, p. 1776 - 1779 (2014/04/17)
For the first time, nucleophilic ring-openings of cyclopropanated 7-oxabenzonorbornadiene were investigated, providing a novel approach to the preparation of 2-methyl-1,2-dihydronaphthalen-1-ols. Satisfactory yields (up to 95%) were achieved using n-Bu2CuCNLi2 as the nucleophile and Et2O as the solvent. The reaction demonstrated successful incorporation of primary, secondary, tertiary and aromatic nucleophiles, as well as ring-openings of substrates bearing arene substituents and C1-bridgehead substituents. A generalized mechanism for these transformations is also proposed.
