55030-25-6

Basic information

• Product Name: 2,4-DI-TERT-BUTYLCYCLOHEXANOL
• Synonyms: 2,4-DI-TERT-BUTYLCYCLOHEXANOL;CYCLOHEXANOL, 2,4-BIS-(1,1-DIMETHYLETHYL)-;2,4-Bis(1,1-dimethylethyl)-1-cyclohexanol;2,4-Di-tert-butyl-1-cyclohexanol
• CAS NO: 55030-25-6
• Molecular Formula: C₁₄H₂₈O
• Molecular Weight: 212.37152
• Mol File: 55030-25-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-DI-TERT-BUTYLCYCLOHEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DI-TERT-BUTYLCYCLOHEXANOL(55030-25-6)
• EPA Substance Registry System: 2,4-DI-TERT-BUTYLCYCLOHEXANOL(55030-25-6)

Safety Data

• Hazardous Substances Data: 55030-25-6(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 71, p. 3798, 1949 DOI: 10.1021/ja01179a062

Upstream product

• 96-76-4 2,4-di-tert-Butylphenol 
• 13019-04-0 2,4-di(tert-butyl)-cyclohexan-1-one 

Downstream Products

• 13019-04-0 2,4-di(tert-butyl)-cyclohexan-1-one 
• 3419-75-8 1,5-di-tert-butyl-cyclohexene 

Relevant articles and documents

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

Compounds for mass coloration of high temperature polymers

The invention relates to novel soluble pigment precursors possessing not only higher thermal stability but also improved solubility characteristics and to a process for mass coloration of high temperature polymers that utilizes these novel soluble pigment precursors. The pigment precursors of the invention are essentially of the formula A(B)x??(I) where x is an integer from 1 to 8, A is the radical of a chromophore of the quinacridone, anthraquinone, perylene, indigo, quinophthalone, indanthrone, isoindolinone, isoindoline, dioxazine, azo, phthalocyanine or diketopyrrolopyrrole series, this radical being linked with xB groups via one or more heteroatoms, these heteroatoms being selected from the group consisting of N, O and S and forming part of the radical A, and B is hydrogen or a group of the formula although at least one B group is not hydrogen and when x is from 2 to 8 the B groups may be identical or different. E1, E2, R1, R2, R3, R4, R7, R11, R14and G1are as defined in the specification. Also claimed are some materials pigmented according to the invention.