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82562-85-4

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82562-85-4 Usage

Chemical Properties

white solid

Check Digit Verification of cas no

The CAS Registry Mumber 82562-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,6 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82562-85:
(7*8)+(6*2)+(5*5)+(4*6)+(3*2)+(2*8)+(1*5)=144
144 % 10 = 4
So 82562-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O/c1-2-3-13-4-8-15(9-5-13)16-10-6-14(12-17)7-11-16/h13-17H,2-12H2,1H3/t13-,14-,15?,16-

82562-85-4Downstream Products

82562-85-4Relevant articles and documents

Synthesis method of trans-4-(trans-4'-alkyl cyclohexyl) cyclohexyl formaldehyde

-

Paragraph 0023; 0024, (2021/06/21)

The invention discloses a preparation method of trans-4-(trans-4'-alkyl cyclohexyl) cyclohexyl formaldehyde. Trans-4-(trans-4'-alkyl cyclohexyl) cyclohexyl formaldehyde is obtained through catalytic oxidation reaction of trans-4-(trans-4'-alkyl cyclohexyl) cyclohexyl methanol, wherein the oxidizing agent is oxygen or air, and the catalytic system comprises a catalyst A, a catalyst B and a catalyst C. The catalyst A is piperidine nitroxide free radicals and derivatives thereof, the catalyst B is nitric oxide equivalent, and the catalyst C is bromide, acid or ferric iron salt. The catalytic system of the synthesis method is efficient and environmentally friendly, the whole reaction process is clean and safe, and the synthesis method has great advantages from the aspect of economy or environmental protection.

Aliphatic Liquid Crystals with Positive Dielectric Anisotropy

Osman, Maged A.,Huynh-Ba, T.

, p. 959 - 963 (2007/10/02)

Cyanoethyl-substituted cyclohexyl cyclohexanoates, bi(cyclohexanes) and phenyl cyclohexanes were synthesized.Their mesomorphic behaviour is compared to that of the corresponding cyano derivatives. (Cyanoethyl)cyclohexyl cyclohexanoates show mesomorphic properties in contrast to the corresponding cyano derivatives.Separation of the cyano substituent from the rigid core of an anisotropic aliphatic compound by methylene groups enhances the thermodynamic stability of its mesophase.In aromatic compounds, the cyanoethyl group leads to lower clearing points.These phenomena are attributed to the influence of steric effects on the packing density and to the dependence of the clearing point on molecular association.

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