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3321-50-4

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3321-50-4 Usage

General Description

1,2-Dicyclohexylethane is a chemical compound with the molecular formula C14H26. It is a colorless liquid with a faint odor and is insoluble in water. It is primarily used as a solvent in various industrial applications, such as in the production of paints, varnishes, and adhesives. It is also used as a reaction medium in organic synthesis and as a lubricant additive in the automotive industry. 1,2-Dicyclohexylethane has low acute toxicity and is considered to have low potential for environmental harm. However, prolonged exposure to high concentrations may cause irritation to the respiratory system and skin. Overall, it is a versatile chemical with various industrial uses but should be handled with care to minimize potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 3321-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3321-50:
(6*3)+(5*3)+(4*2)+(3*1)+(2*5)+(1*0)=54
54 % 10 = 4
So 3321-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H26/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h13-14H,1-12H2

3321-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexylethylcyclohexane

1.2 Other means of identification

Product number -
Other names 1,2-Dicyclohexyl-aethan

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:3321-50-4 SDS

3321-50-4Relevant articles and documents

Studies towards the Total Synthesis of Drimentine C. Preparation of the AB and CDEF Ring Fragments

Pound, Sarah M.,Underwood, Steven J.,Douglas, Christopher J.

, p. 2448 - 2453 (2020)

The drimentine family is a class of hybrid isoprenoids derived from actinomycete bacteria. Members of this family display weak antitumor and antibacterial activity. Herein we report our efforts toward the total synthesis of drimentine C using three distinct approaches incorporating palladium-catalyzed cyanoamidation, reductive cross-coupling, and photoredox-catalyzed α-alkylation of an aldehyde as key steps. Our synthetic efforts use a convergent synthesis to assemble the terpenoid and alkaloid portions of drimentine C from readily available l-tryptophan, l-proline, and (+)-sclareolide.

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

-

Paragraph 0094-0095; 0123-0125; 0127-0130, (2021/05/29)

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.

One-Pot Conversion of Lignin into Naphthenes Catalyzed by a Heterogeneous Rhenium Oxide-Modified Iridium Compound

Li, Xinxin,Zhang, Bo,Pan, Xiaoli,Ji, Jianwei,Ren, Yujing,Wang, Hua,Ji, Na,Liu, Qiying,Li, Changzhi

, p. 4409 - 4419 (2020/03/04)

The direct transformation of lignin into fuels and chemicals remains a huge challenge because of the recalcitrant and complicated structure of lignin. In this study, rhenium oxide-modified iridium supported on SiO2 (Ir-ReOx/SiO2) is employed for the one-pot conversion of various lignin model compounds and lignin feedstocks into naphthenes. Up to 100 percent yield of cyclohexane from model compounds and 44.3 percent yield of naphthenes from lignin feedstocks are achieved. 2 D HSQC NMR spectroscopy before and after the reaction confirms the activity of Ir-ReOx/SiO2 in the cleavage of the C?O bonds and hydrodeoxygenation of the depolymerized products. H2 temperature-programmed reduction, temperature-programmed desorption of NH3, IR spectroscopy of pyridine adsorption, X-ray photoelectron spectroscopy, X-ray absorption fine structure analysis, and control experiments reveal that a synergistic effect between Ir and ReOx in Ir-ReOx/SiO2 plays a crucial role in the high performance; ReOx is mainly responsible for the cleavage of C?O bonds, whereas Ir is responsible for hydrodeoxygenation and saturation of the benzene rings. This methodology opens up an energy-efficient route for the direct conversion of lignin into valuable naphthenes.

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