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Tricyclohexylmethane, also known as tricyclohexylmethylmethane or tricyclohexylmethyl, is a chemical compound with the molecular formula C21H36. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. Tricyclohexylmethane. is derived from the methane molecule, where each hydrogen atom is replaced by a cyclohexyl group, resulting in a highly symmetrical and sterically hindered structure. Tricyclohexylmethane is primarily used as a chemical intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure provides it with interesting chemical properties, such as resistance to oxidation and thermal stability, which make it a valuable component in the development of new materials and reactions.

1610-24-8

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1610-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1610-24:
(6*1)+(5*6)+(4*1)+(3*0)+(2*2)+(1*4)=48
48 % 10 = 8
So 1610-24-8 is a valid CAS Registry Number.

1610-24-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dicyclohexylmethylcyclohexane

1.2 Other means of identification

Product number -
Other names Methane,tricyclohexyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1610-24-8 SDS

1610-24-8Relevant academic research and scientific papers

Cyclohexyl Rings in Spatial Proximity: Stereochemistry of Tricyclohexylmethane

Columbus, Ishay,Biali, Silvio E.

, p. 7029 - 7035 (1993)

The static and dynamic stereochemistry of tricyclohexylmethane (2) is analyzed.The 13C nad 1H NMR of 2 were assigned by means of the 2D NMR techniques INADEQUATE and DQF COSY.Molecular mechanics calculations were performed in order to estimate the influen

The structure of tricyclohexylmethane

Gillies, D. G.,Luff, S.,Smith, G. W.,Sutcliffe, L. H.

, p. 113 - 122 (1994)

Tricyclohexylmethane has a melting point close to ambient temperature.Nevertheless the X-ray structure has been determined.The crystal is chiral but its chirality could not be established.The solid is unusual in that the atomic volume per carbon atoms is

Radical deoxygenation of tertiary alcohols via trifluoroacetates

Kim, Joong-Gon,Cho, Dae Hyan,Jang, Doo Ok

, p. 3031 - 3033 (2007/10/03)

Trifluoroacetates of tertiary alcohols undergo deoxygenation by Ph 2SiH2 in the presence of (tBuO)2 in excellent yields of the deoxy products without affecting the stereochemistry at β-carbon.

CATALYTIC CONVERSIONS OF TRICYCLOHEXYLMETHANE.

Gavrilov,Kosnikovskaya,Muratalieva

, p. 123 - 126 (2007/10/02)

The authors have achieved low-temperature catalytic isomerization of tricyclohexylmethane under the influence of Lewis acids, special attention being devoted to formation of tricyclic structures of the admantane type. It is found that the effects of alumi

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