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(4aS,8aS)-Octahydronaphthalen-1(2H)-one is a cyclic ketone with a molecular formula of C10H16O. It is a chiral compound, meaning it has a non-superimposable mirror image, and it adopts a specific conformation with the 4aS and 8aS configurations. This organic compound is a derivative of naphthalene, featuring a six-membered ring fused to a four-membered ring, and it contains a ketone functional group at the 1-position. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is also known for its potential applications in the field of materials science, particularly in the development of new polymers and other advanced materials.

6102-32-5

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6102-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6102-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6102-32:
(6*6)+(5*1)+(4*0)+(3*2)+(2*3)+(1*2)=55
55 % 10 = 5
So 6102-32-5 is a valid CAS Registry Number.

6102-32-5Upstream product

6102-32-5Downstream Products

6102-32-5Relevant academic research and scientific papers

FUNCTIONALISATION OF SATURATED HYDROCARBONS. Part X. A COMPARATIVE STUDY OF CHEMICAL AND ELECTROCHEMICAL PROCESSES (GIF AND GIF-ORSAY SYSTEMS) IN PYRIDINE, IN ACETONE AND IN PYRIDINE-CO-SOLVENT MIXTURES

Belavoine, Gilbert,Barton, Derek H. R.,Boivin, Jean,Gref, Aurore,Coupanec, Pascale Le,et al.

, p. 1091 - 1106 (2007/10/02)

Six saturated hydrocarbons (cyclohexane, 3-ethylpentane, methylcyclopentane, cis- and trans-decalin and adamantane) were oxidised by the Gif system (iron catalyst, oxygen, zinc, carboxylic acid) and its electrochemical equivalent (Gif-Orsay system).Results obtained using various solvents (pyridine, acetone, pyridine-acetone mixtures) were similar for both systems.Total or partial replacement of pyridine with acetone affects the selectivity for secondary positions and lowers the ketone/secondary alcohol ratio.The formation of the same ratio of cis- and trans-decal-9-ol from both cis- and trans-decalin clearly demonstrates that tertiary alcohols result from a mechanism essentially radical in nature.

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