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1-Decylcyclohexane, with the molecular formula C18H34, is a colorless liquid characterized by a slight odor. It is insoluble in water but readily soluble in organic solvents. This chemical compound is known for its low volatility and high chemical stability, making it a versatile substance in various industrial applications.

1795-16-0

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1795-16-0 Usage

Uses

Used in the Chemical Industry:
1-Decylcyclohexane is used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances and its compatibility with organic materials.
Used in the Fragrance Industry:
It serves as a component in the production of fragrances, leveraging its solubility in organic solvents to help carry and stabilize scent compounds.
Used in the Paint and Coating Industry:
1-Decylcyclohexane is used in the formulation of paints and coatings, contributing to their performance characteristics such as drying time and durability.
Used in the Manufacturing of Consumer Products:
It is incorporated into household cleaners, personal care products, and automotive fluids, where its solvent properties aid in the effective dissolution and application of these products.
Used as a Lubricant in Mechanical Processes:
Due to its low volatility and high chemical stability, 1-Decylcyclohexane is utilized as a lubricant in various mechanical applications, reducing friction and wear on machinery parts.

Check Digit Verification of cas no

The CAS Registry Mumber 1795-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1795-16:
(6*1)+(5*7)+(4*9)+(3*5)+(2*1)+(1*6)=100
100 % 10 = 0
So 1795-16-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H32/c1-2-3-4-5-6-7-8-10-13-16-14-11-9-12-15-16/h16H,2-15H2,1H3

1795-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name decylcyclohexane

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-decan

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:1795-16-0 SDS

1795-16-0Downstream Products

1795-16-0Relevant articles and documents

Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling

Hatakeyama, Takuji,Hashimoto, Toru,Kathriarachchi, Kalum K. A. D. S.,Zenmyo, Takeshi,Seike, Hirofumi,Nakamura, Masaharu

supporting information; experimental part, p. 8834 - 8837 (2012/10/08)

Chemoselective Suzuki-Miyaura coupling of primary and secondary alkyl halides is realized by using an iron/Xantphos catalyst. Primary and secondary alkyl bromides undergo the reaction to give the coupling products in good yields. Application to the synthe

Cobalt-catalyzed cross-coupling reaction between functionalized primary and secondary alkyl halides and aliphatic Grignard reagents

Cahiez, Gerard,Chaboche, Christophe,Duplais, Christophe,Giulliani, Arianna,Moyeux, Alban

supporting information; experimental part, p. 1484 - 1488 (2009/07/01)

The coupling of primary and secondary unactivated alkyl bromides with alkyl-Grignard reagents was performed in good yields under mild conditions by using a new catalytic system: consisting of cobalt chloride and tetramethylethylenediamine (CoCl2·2 LiI, 4TMEDA). The reaction is very chemoselective since ketone, ester and nitrile functions are tolerated.

A highly selective arene hydrogenation catalyst that operates in ionic liquid

Boxwell, Clive J.,Dyson, Paul J.,Ellis, David J.,Welton, Thomas

, p. 9334 - 9335 (2007/10/03)

The synthesis and structural characterization of [Ru(η6-p-cymene)(η2-TRIPHOS)Cl][PF6] is described. The complex is a highly active, homogeneous arene hydrogenation catalyst that is selective toward the hydrogenation of aromatic rings in preference to alkenes, as demonstrated by the hydrogenation of allylbenzene to allylcyclohexane. The catalyst operates in both dichloromethane and ionic liquids and undergoes no decomposition in the latter solvent. Copyright

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