1130-20-7 Usage
Uses
Used in Fragrance and Flavoring Industry:
Spiro5.6dodecan-7-ol is used as a fragrance and flavoring agent for its ability to impart a pleasant, long-lasting odor to various products. Its fruity scent makes it suitable for use in perfumes, colognes, and other scented products.
Used in Solvent Applications:
In the chemical industry, Spiro5.6dodecan-7-ol is used as a solvent due to its ability to dissolve a wide range of substances. This makes it useful in various chemical processes and reactions.
Used in Synthesis of Organic Compounds:
Spiro5.6dodecan-7-ol is also utilized in the synthesis of other organic compounds, serving as a key intermediate in the production of various chemical products. Its unique structure allows it to be a versatile building block in organic chemistry.
Used in Consumer Products:
Spiro5.6dodecan-7-ol is used in the formulation of consumer products, such as cleaning agents, air fresheners, and personal care products, due to its safe usage when following regulations and guidelines. Its pleasant scent and compatibility with other ingredients make it a valuable addition to these products.
Check Digit Verification of cas no
The CAS Registry Mumber 1130-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1130-20:
(6*1)+(5*1)+(4*3)+(3*0)+(2*2)+(1*0)=27
27 % 10 = 7
So 1130-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O/c13-11-7-3-1-4-8-12(11)9-5-2-6-10-12/h11,13H,1-10H2
1130-20-7Relevant academic research and scientific papers
Mechanism of titanocene-mediated epoxide opening through homolytic substitution
Gansaeuer, Andreas,Barchuk, Andriy,Keller, Florian,Schmitt, Martin,Grimme, Stefan,Gerenkamp, Mareike,Mueck-Lichtenfeld, Christian,Daasbjerg, Kim,Svith, Heidi
, p. 1359 - 1371 (2007/10/03)
The mechanism of titanocene-mediated epoxide opening was studied by a combination of voltammetric, kinetic, computational, and synthetic methods. With the aid of electrochemical investigations the nature of a number of Ti(III) complexes in solution was established. In particular, the distribution of monomeric and dimeric Ti(III) species was found to be strongly affected by the exact steric conditions. The overall rate constants of the reductive epoxide opening were determined for the first time. These data were employed as the basis for computational studies of the structure and energies of the epoxide-titanocene complexes, the transition states of epoxide opening, and the β-titanoxy radicals formed. The results obtained provide a structural basis for the understanding of the factors determining the regioselectivity of ring opening and match the experimentally determined values. By employing substituted titanocenes even more selective epoxide openings could be realized, Moreover, by properly adjusting the steric demands of the catalysts and the substrates the first examples of reversible epoxide openings were designed.
