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16728-52-2

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16728-52-2 Usage

General Description

3-(cyclohexyloxy)propiononitrile is a chemical compound with the molecular formula C9H15NO, consisting of a propiononitrile group attached to a cyclohexyl ether moiety. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 3-(cyclohexyloxy)propiononitrile is a colorless liquid with a faint odor, and is stable under normal conditions. It is a versatile building block in organic synthesis, and its reactivity allows for the formation of a wide range of structurally diverse compounds. However, it should be handled with caution as it may be toxic if ingested or inhaled, and can irritate the eyes and skin upon contact.

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 articles and documents

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.

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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