6248-88-0 Usage
Uses
Used in Chemical Industry:
1,3,3-Trimethylnorbornane is used as a building block for the synthesis of various organic compounds and materials. Its unique bicyclic structure and methyl group substitutions make it a valuable intermediate in the production of different chemicals, including pharmaceuticals, fragrances, and other specialty chemicals.
Used in Pharmaceutical Industry:
1,3,3-Trimethylnorbornane is used as a starting material for the development of new drugs and pharmaceutical compounds. Its structural properties allow for the creation of novel molecules with potential therapeutic applications, contributing to the advancement of medical treatments.
Used in Fragrance Industry:
1,3,3-Trimethylnorbornane is used as a component in the formulation of fragrances and perfumes. Its unique chemical structure may contribute to the development of new scents and aromas, enhancing the variety and complexity of fragrances available in the market.
Used in Research and Development:
1,3,3-Trimethylnorbornane is used as a research compound for studying the properties and behavior of monoterpenes and other related organic compounds. Its unique structure provides valuable insights into the chemical and physical characteristics of this class of compounds, aiding in the development of new materials and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6248-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6248-88:
(6*6)+(5*2)+(4*4)+(3*8)+(2*8)+(1*8)=110
110 % 10 = 0
So 6248-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-9(2)7-10(3)5-4-8(9)6-10/h8H,4-7H2,1-3H3
6248-88-0Relevant academic research and scientific papers
Ni-Cu/Al2O3 containing O.1percent CeO2: A New Catalyst for Dehydrogenation of Alcohols
Singh, Satendra,Dev, Sukh
, p. 463 - 468 (2007/10/02)
A highly active and selective catalyst containing 10percent Ni-Cu (atomic ratio 7 : 3) supported on alumina and promoted with 0.1percent cerium oxide was developed for dehydrogenation of secondary alcohols into corresponding ketones in vapour phase.
THE CHEMISTRY OF 1,3,4-THIADIAZOLINE-2-SPIRO-2'-FENCHANE.
Huisgen, Rolf,Mloston, Grzegorz,Proebstl, Albert
, p. 4431 - 4434 (2007/10/02)
Diazomethane adds to one of the two faces of the sterically hindered thiofenchone furnishing the title compound wich extrudes N2 at 46 deg C whith t1/2=22 min; the thiofenchone S-methylide is intercepted by dipolarophiles and acts as a base in reactions with methanol, thiophenol and acetic acid, in the latter case accompanied by skeletal rearrangement.
