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3-(cyclohexyloxy)propiononitrile is a chemical compound characterized by the molecular formula C9H15NO. It features a propiononitrile group connected to a cyclohexyl ether moiety, forming a colorless liquid with a faint odor. This versatile intermediate is stable under normal conditions and is widely utilized in the synthesis of pharmaceuticals and agrochemicals due to its reactivity, which facilitates the creation of structurally diverse compounds. However, it requires careful handling as it may pose health risks if ingested, inhaled, or if it comes into contact with the eyes or skin.

16728-52-2

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16728-52-2 Usage

Uses

Used in Pharmaceutical Industry:
3-(cyclohexyloxy)propiononitrile is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of a broad spectrum of medicinal compounds. Its reactivity and structural diversity make it a valuable component in developing new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(cyclohexyloxy)propiononitrile is employed as an intermediate in the production of pesticides and other agrochemicals, leveraging its chemical properties to enhance the effectiveness of these products in agricultural applications.
Used in Organic Synthesis:
3-(cyclohexyloxy)propiononitrile is utilized as a versatile building block in organic synthesis, where its reactivity allows chemists to create a wide range of structurally diverse compounds for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 16728-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16728-52:
(7*1)+(6*6)+(5*7)+(4*2)+(3*8)+(2*5)+(1*2)=122
122 % 10 = 2
So 16728-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO/c10-7-4-8-11-9-5-2-1-3-6-9/h9H,1-6,8H2

16728-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyclohexyloxypropanenitrile

1.2 Other means of identification

Product number -
Other names 3-Cyclohexyloxy-propionsaeure-nitril

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:16728-52-2 SDS

16728-52-2Relevant academic research and scientific papers

Formation of a New, Strongly Basic Nitrogen Anion by Metal Oxide Modification

Tamura, Masazumi,Kishi, Ryota,Nakayama, Akira,Nakagawa, Yoshinao,Hasegawa, Jun-Ya,Tomishige, Keiichi

, p. 11857 - 11867 (2017/09/08)

Development of new hybrid materials having unique and unprecedented catalytic properties is a challenge for chemists, and heterogeneous-homogeneous hybrid catalysts have attracted much attention because of the preferable and exceptional properties that are highly expected to result from combination of the components. Base catalysts are widely used in organic synthesis as key materials, and a new class of base catalysts has made a large impact from academic and industrial viewpoints. Here, a principle for creating a new strong base by hybridization of homogeneous and heterogeneous components is presented. It is based on the modification of organic compounds with metal oxides by using the acid-base property of metal oxides. Based on kinetic and DFT studies, combination of CeO2 and 2-cyanopyridine drastically enhanced the basicity of 2-cyanopyridine by a factor of about 109 (~9 by pKa (in CH3CN)), and the pKa was estimated to be ~21, which locates it in the superbase category. 2-Cyanopyridine and CeO2 formed a unique adsorption complex via two interaction modes: (i) coordinative interaction between the Ce atom of CeO2 and the N atom of the pyridine ring in 2-cyanopyridine, and (ii) covalent interaction between the surface O atom of CeO2 and the C atom of the CN group in 2-cyanopyridine by addition of the lattice oxygen of CeO2 to the CN group of 2-cyanopyridine. These interactions established a new, strongly basic site of N- over the CeO2 surface.

Catalytic Olefin hydroalkoxylation by nano particles of pollucite

Zamanian, Sara,Kharat, Ali Nemati

, p. 981 - 986 (2015/06/25)

The catalytic hydroalkoxylation of α,β-unsaturated esters, nitriles, and ethers with aliphatic and aromatic alcohols over pollucite using thermal and microwave-assisted methods was investigated. To study the effect of the alcohol structures on the mechanism of the hydroalkoxylation reaction, different alcohols, such as methanol to butanol, cyclohexanol, phenol, and 2-ethylhexanol were used. The activities of pollucite, in contrast to other basic solids, were scarcely affected by the presence of air and moisture. The correlation between alcohol acidity and reaction activity is discussed. The prepared pollucite was characterized by X-ray diffraction, volumetric nitrogen adsorption surface area analysis, and CO2 temperature-programmed desorption. Scanning electron microscopy analysis revealed that the size of the modified nano catalyst particles was under 40nm.

Solid sodium stannate as a high-efficiency superbase catalyst for anti-Markovnikov hydroamination and hydroalkoxylation of electron-deficient olefins under mild conditions

Zhang, Shuguo,Wei, Yudan,Yin, Shuangfeng,Au, Chak-Tong

, p. 712 - 716 (2013/01/09)

A solid superbase with H- above 26.5 has been obtained through thermal treatment of sodium stannate hydrate. It was found to be an efficient catalyst for anti-Markovnikov hydroamination and hydroalkoxylation of electron-deficient olefins under mild conditions.

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