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Cyclopentanamine, N-cyclopentylidene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27721-49-9

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27721-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27721-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,2 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27721-49:
(7*2)+(6*7)+(5*7)+(4*2)+(3*1)+(2*4)+(1*9)=119
119 % 10 = 9
So 27721-49-9 is a valid CAS Registry Number.

27721-49-9SDS

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 N-cyclopentylcyclopentanimine

1.2 Other means of identification

Product number -
Other names N-Cyclopentyliden-cyclopentylamin

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:27721-49-9 SDS

27721-49-9Downstream Products

27721-49-9Relevant academic research and scientific papers

Morphology-Tuned Activity of Ru/Nb2O5 Catalysts for Ketone Reductive Amination

Guo, Wanjun,Tong, Tao,Liu, Xiaohui,Guo, Yong,Wang, Yanqin

, p. 4130 - 4138 (2019/05/24)

Amines are important compounds in natural products and medicines. Specifically, cyclopentylamine is one of the value-added chemicals widely used in the production of pesticides, cosmetics and medicines. In this work, three Ru/Nb2O5 catalysts with different Nb2O5 morphologies were used in the reductive amination of cyclopentanone under mild reaction conditions (90 °C, 2 MPa H2), among which 1 %Ru/Nb2O5?L catalyst exhibits best performance with the yield of cyclopentylamine reaching 84 %. This catalytic system is stable and has not significant deactivation even after 5 runs in the durability test. In addition, this catalyst can be extended to a series of aldehydes/ketones. Further comprehensive characterizations (XPS analysis and CO-adsorption DRIFT) reveal that the electronic effect of Ru species can be ruled out; instead, the activity of the catalyst is strongly influenced by the geometric effect. Layered Nb2O5 material possesses the highest surface area, resulting in the highest Ru dispersion, and therefore shows the highest catalytic activity. The in-situ DRIFT-MS technique was also used to reveal and understand the reaction mechanism. It is found that Ru species play a key role in activating carbonyl groups. This study illustrates a promising application of Ru/Nb2O5-Layer catalyst in the synthesis of amine and provides an understanding to the reaction mechanism.

Oxidation of amines over alumina based catalysts

Rakottyay, Karol,Kaszonyi, Alexander,Vají?ek, Stanislav

experimental part, p. 33 - 41 (2010/08/22)

Amines were oxidized by molecular oxygen in the vapor phase at atmospheric pressure over alumina and silicotungstic acid/alumina catalysts. The study is focused on the influence of structure of amine and catalyst properties on the composition of the main reaction products and byproducts. Coating of γ-Al2O3 with silicotungstic acid or its semisalt can significantly enhance its catalytic activity in amine oxidation. The adsorption of amine on weak acidic sites of catalyst is essential for its oxidation to main reaction products. Cycloalkylamines are oxidized mainly to cyclic oximes (selectivity up to 64%) and Schiff bases of appropriate cycloalkanone and cycloalkylamine (selectivity up to 38%). Mainly nitriles (selectivity up to 55%) and appropriate Schiff bases (selectivity up to 54%) were observed in the oxidation products of primary alkylamines. Their molar ratio depends on the catalyst acidity and reaction conditions. 1,6-Hexanediamine is oxidized mainly to caprolactam (yield 48%) and other cyclic lactames and Schiff bases as well as to dinitrile (yield 13%).

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