51478-26-3 Usage
Description
1-(3-methylbutyl)cyclohexanol, also known as Isohexylcyclohexanol, is a chemical compound characterized by its molecular formula C12H24O. It is a colorless liquid with a distinct floral scent, making it a popular choice for various applications across different industries.
Uses
Used in Perfumery and Fragrance Industry:
1-(3-methylbutyl)cyclohexanol is used as a key ingredient in the creation of perfumes and fragrances due to its appealing floral odor. Its distinctive scent adds depth and complexity to the fragrances, enhancing the overall sensory experience for consumers.
Used in Food Industry:
In the food industry, 1-(3-methylbutyl)cyclohexanol is utilized as a flavoring agent to impart a pleasant taste and aroma to various food products. Its ability to add a unique flavor profile makes it a valuable addition to the culinary world.
Used in Pharmaceutical Industry:
1-(3-methylbutyl)cyclohexanol holds potential in the pharmaceutical industry as a precursor for the synthesis of various drugs. Its unique chemical structure allows for the development of new and innovative medications, contributing to the advancement of healthcare solutions.
Used in Industrial Processes:
As a solvent, 1-(3-methylbutyl)cyclohexanol is employed in various industrial processes. Its versatility as a solvent makes it a valuable component in the production of different products, from chemicals to coatings and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 51478-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,7 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51478-26:
(7*5)+(6*1)+(5*4)+(4*7)+(3*8)+(2*2)+(1*6)=123
123 % 10 = 3
So 51478-26-3 is a valid CAS Registry Number.
51478-26-3Relevant articles and documents
The Heterogeneous Catalytic Hydrogenation of Cumulated Allene-cyclopropanes: 1-(2'-Methylpropenylidene)-7-bicycloheptane
Cromble, Leslie,Fernando, Candida E. C.
, p. 1501 - 1518 (2007/10/03)
The formation of products from the heterogeneous solution phase catalytic hydrogenation of the title compound 1 in methanol over supported platinum and palladium catalysts has been studied using 'snapshot analysis' graphs. As expected from 'catalyst hindrance' considerations, the major first formed product with both metals is the conjugated cis-olefin-cyclopropane 7, the trans-isomer 8 being made for comparison by sodium in liquid ammonia reduction. Products appear and disappear during the hydrogenations leaving, at the cassation of reaction in the case of platinum catalyst, 75 percent of cyclopropane 6 and 25 percent of saturated hydrocarbon 3. Use of a palladium reverses the quantitative situation - 12 percent cyclopropane 6 and 88 percent of hydrocarbon 3. If in the title allene-cyclopropane structure 1 a methyl is inserted at position 1 of the cyclopropyl as in 13, complete hydrogenation over a palladium catalyst occurs with cleavage of the cyclopropane from the less hindered side forming a quaternary centre 14 in high yield. Catalytic hydrogenation of a related conjugated diene having one double bond cumulated with a cyclopropane ring 12 is also considered. Dimethylallene carbene reacts selectively towards an (E)-linkage of (Z)-(E)-(E)-cyclododeca-1,5,9-triene giving 19 as the crystalline product.
