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N-cyclopentyl-N-cyclopropylamine is an organic compound with the molecular formula C10H19N. It is a derivative of cyclopropylamine, featuring a cyclopentyl group attached to the nitrogen atom. This cyclic amine is known for its unique structure, which contributes to its chemical properties and potential applications. It is a colorless liquid at room temperature and is soluble in organic solvents. Due to its cyclic nature, it can be used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's reactivity and stability make it a valuable intermediate in organic synthesis, particularly in the preparation of complex molecules that require the presence of cyclic amines.

873-59-6

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873-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873-59-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 873-59:
(5*8)+(4*7)+(3*3)+(2*5)+(1*9)=96
96 % 10 = 6
So 873-59-6 is a valid CAS Registry Number.

873-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Cyclopropylcyclopentanamine

1.2 Other means of identification

Product number -
Other names N-Cyclobutyl-N-cyclopropylamine

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:873-59-6 SDS

873-59-6Relevant academic research and scientific papers

A biocatalytic cascade for the amination of unfunctionalised cycloalkanes

Tavanti, Michele,Mangas-Sanchez, Juan,Montgomery, Sarah L.,Thompson, Matthew P.,Turner, Nicholas J.

supporting information, p. 9790 - 9793 (2017/12/08)

Here we describe a one-pot, three-enzyme, cascade involving a cytochrome P450 monooxygenase, an alcohol dehydrogenase and a reductive aminase for the synthesis of secondary amines from cycloalkanes. Amine product concentrations of up to 19.6 mM were achieved. The preparative scale amination of cyclohexane was also demonstrated with a space-time yield of 2 g L-1 d-1.

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