1795-17-1 Usage
General Description
Dodecylcyclohexane is a chemical compound that belongs to the class of cycloalkanes and alkyl groups. It is a colorless liquid with a mild odor, and it is insoluble in water but soluble in organic solvents. Dodecylcyclohexane is widely used as a solvent in various industrial applications, such as in the manufacturing of paints, coatings, adhesives, and polymers. It is also used as a chemical intermediate in the production of other organic compounds. Additionally, dodecylcyclohexane has surfactant properties, making it suitable for use in the formulation of cleaning and personal care products. Overall, dodecylcyclohexane is a versatile chemical with a range of industrial applications due to its solvency and surfactant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1795-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1795-17:
(6*1)+(5*7)+(4*9)+(3*5)+(2*1)+(1*7)=101
101 % 10 = 1
So 1795-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H36/c1-2-3-4-5-6-7-8-9-10-12-15-18-16-13-11-14-17-18/h18H,2-17H2,1H3
1795-17-1Relevant articles and documents
DISSOLVING METAL REDUCTION WITH CROWN ETHER --- REDUCTIVE REMOVAL OF ISOCYANO GROUPS
Ohsawa, Tomihiko,Mitsuda, Naoki,Nezu, Jun'ichi,Oishi, Takeshi
, p. 845 - 846 (1989)
Toluene radical anion generated from K metal and toluene with the assistance of crown ether has been proven effective for reductive removal of aliphatic isocyano groups.
Nickel/Cobalt-Catalyzed C(sp3)-C(sp3) Cross-Coupling of Alkyl Halides with Alkyl Tosylates
Komeyama, Kimihiro,Michiyuki, Takuya,Osaka, Itaru
, p. 9285 - 9291 (2019/10/11)
The C(sp3)-C(sp3) cross-coupling of alkyl halides with alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts in the presence of a manganese reductant. This method provides a straightforward route to a diverse set of not only secondary-primary but also primary-primary C(sp3)-C(sp3) linkages under mild conditions without using alkyl-metallic reagents. Mechanistic studies suggest the formation of alkyl radicals from both alkyl halides and alkyl tosylates. Additionally, cross-coupling could be applied to the short-step synthesis of a histone deacetylase inhibitor, Vorinostat.
