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1,1-dimethyl-1,2,3,4-tetrahydronaphthalen-2-ol is a complex organic compound with the molecular formula C12H16O. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a methyl group attached to the first carbon and a hydroxyl group at the second carbon of the tetrahydro ring. 1,1-dimethyl-1,2,3,4-tetrahydronaphthalen-2-ol is characterized by its unique structure, which features a saturated six-membered ring fused to a partially saturated five-membered ring. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and potential for further functionalization. The compound's stability, reactivity, and solubility in organic solvents make it a valuable building block in organic synthesis, particularly in the preparation of complex molecules with potential applications in the fields of medicine and chemistry.

1865-95-8

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1865-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1865-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1865-95:
(6*1)+(5*8)+(4*6)+(3*5)+(2*9)+(1*5)=108
108 % 10 = 8
So 1865-95-8 is a valid CAS Registry Number.

1865-95-8Relevant academic research and scientific papers

Cyclialkylation of arylalkyl epoxides with solid acid catalysts

Elings, Jacob A.,Downing, Roger S.,Sheldon, Roger A.

, p. 837 - 846 (2007/10/03)

Solid acids, such as zeolites and clays, catalyse the intramolecular hydroxyalkylation (cyclialkylation) of several arylalkyl epoxides in moderate to excellent conversions and selectivities. The use of solid acids in these cyclialkylations provides a cleaner, better alternative to conventional Lewis and Bronsted acids, enabling a more facile workup of reaction mixtures and, in several cases, better selectivities.

Friedel-Crafts Cyclialkylations of Some Epoxides. 3. Cyclizations of Tertiary and Meta-Substituted Arylalkyl Epoxides

Taylor, Stephen K.,Blankespoor, Curtis L.,Harvey, Suzanne M.,Richardson, Lynell J.

, p. 3309 - 3312 (2007/10/02)

The intramolecular cyclization of aryl groups to tertiary epoxide position was investigated, and the results were used to test the applicability of Baldwin's rules to this specific class of reactions.As a probe into mechanism of reactions studied earlier, the cyclizations of some meta-substituted 1,2-epoxy-5-phenylpentanes were examined to determine positional selectivities.The data obtained were compared with those of other studies, and comments are made on the reaction mechanism.

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