13254-34-7 Usage
Uses
Used in Perfumery:
2,6-Dimethyl-2-heptanol is used as a fragrance ingredient for its floral scent, contributing to the overall aroma of perfumes and colognes. Its delicate and pleasant odor makes it a valuable addition to various fragrance formulations.
Used in Insect Repellent Compounds:
2,6-Dimethyl-2-heptanol is used as a key component in the preparation of 3''-ketoglycoside compounds, which possess insect repellent effects. These compounds can be utilized in the development of insect repellent products, providing protection against biting insects and potentially reducing the spread of insect-borne diseases.
Used in Chemical Research and Analysis:
Due to its unique chemical properties and synthetic nature, 2,6-Dimethyl-2-heptanol is also used in the preparation and analytical study of various chemical compounds. This application aids in the advancement of chemical research and the development of new products and materials.
Production Methods
2,6-
Dimethyl-2-heptanol is prepared from the reaction of methyl
heptenone and methyl magnesium halide, followed by
hydrogenation.
Flammability and Explosibility
Notclassified
Trade name
Dimetol? (Givaudan).
Check Digit Verification of cas no
The CAS Registry Mumber 13254-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13254-34:
(7*1)+(6*3)+(5*2)+(4*5)+(3*4)+(2*3)+(1*4)=77
77 % 10 = 7
So 13254-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-8(2)6-5-7-9(3,4)10/h8,10H,5-7H2,1-4H3
13254-34-7Relevant articles and documents
Mono- and Di-μ-hydrido-bridged carbodications in acyclic systems
Sun, Fang,Sorensen
, p. 77 - 81 (2007/10/02)
μ-Hydrido-bridging in carbocations (C-H-C)+ involves a two-electron three-center bond. Such structures have previously been observed only when the two carbons are part of a medium ring (monocyclic, bicyclic, or tricyclic frameworks). Using appropriately constructed carbodications, acyclic systems are now shown to form such structures, including a novel example containing two μ-hydrido-bridged units.
Rates and Alkyl Group Size in Solvolysis of Alkyl Derivatives
Orlovic, Mirko,Kronja, Olga,Humski, Kresimir,Borcic, Stanko,Polla, Eugenio
, p. 3253 - 3256 (2007/10/02)
The logarithm of solvolysis rate constants in 80percent aqueous ethanol of 1,1-dimethyl-1-alkyl chlorides 1 and 1-phenyl-1-alkyl chlorides 2 decrease monotonically with increasing number of carbon atoms in the alkyl group.The first member of both series deviates from the corresponding correlation lines which have the some slope.In contrast, solvolysis rates in 80percent aqueous ethanol of 1-methyl-1-alkyl tosylates 3 do not depend upon the size of the alkyl group.The results are rationalized in terms of a mechanism that is very similar in reactions of series 1 and 2 but different from that of series 3.
