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3-(Cyclopentyloxy)-4-methoxybenzonitrile, a chemical compound with the molecular formula C14H15NO2, is a nitrile derivative characterized by a benzene ring with a methoxy group and a cyclopentyl ether group. It is a versatile intermediate in organic chemistry, known for its unique properties and behavior in various conditions, making it valuable for the production of drugs, biologically active molecules, and more complex chemical structures.

159783-16-1

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159783-16-1 Usage

Uses

Used in Pharmaceutical Research:
3-(Cyclopentyloxy)-4-methoxybenzonitrile is used as a key intermediate in the synthesis of various types of drugs and biologically active molecules. Its unique structure and properties contribute to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Research:
In the agrochemical industry, 3-(Cyclopentyloxy)-4-methoxybenzonitrile serves as a valuable intermediate for the development of new agrochemicals. Its chemical properties allow for the creation of compounds with potential applications in crop protection, pest control, and other agricultural areas.
Used in Organic Synthesis:
3-(Cyclopentyloxy)-4-methoxybenzonitrile is used as a building block in the synthesis of more complex chemical structures. Its versatility and reactivity make it an essential component in the creation of advanced organic compounds for various applications, including materials science, specialty chemicals, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 159783-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159783-16:
(8*1)+(7*5)+(6*9)+(5*7)+(4*8)+(3*3)+(2*1)+(1*6)=181
181 % 10 = 1
So 159783-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-15-12-7-6-10(9-14)8-13(12)16-11-4-2-3-5-11/h6-8,11H,2-5H2,1H3

159783-16-1SDS

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-cyclopentyloxy-4-methoxybenzonitrile

1.2 Other means of identification

Product number -
Other names 3-cyclopentyloxy-4-methoxybenzenecarbonitrile

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:159783-16-1 SDS

159783-16-1Relevant academic research and scientific papers

Design and Synthesis of 3,5-Disubstituted-1,2,4-Oxadiazoles as Potent Inhibitors of Phosphodiesterase4B2

Kumar, Dalip,Patel, Gautam,Vijayakrishnan, Lalitha,Dastidar, Sunanda G.,Ray, Abhijit

scheme or table, p. 810 - 818 (2012/06/18)

A series of 3,5-disubstituted-1,2,4-oxadiazoles has been prepared and evaluated for phosphodiesterase inhibition (PDE4B2). Among the prepared 3,5-disubstituted-1,2,4-oxadiazoles, compound 9a is the most potent inhibitor (PDE4B2 IC50=5.28μm). Structure-activity relationship studies of 3,5-disubstituted-1,2,4-oxadiazoles revealed that substituents 3-cyclopentyloxy-4-methoxyphenyl group at 3-position and cyclic ring bearing heteroatoms at 5-position are important for activity. Molecular modeling study of the 3,5-disubstituted-1,2,4-oxadiazoles with PDE4B has shown similar interactions of 3-cyclopentyloxy-4-methoxyphenyl group; however, heteroatom ring is slightly deviating when compared to Piclamilast. 3-(3-Cyclopentyloxy-4-methoxyphenyl)-5-(piperidin-4-yl)-1,2,4-oxadiazole (9a) exhibited good analgesic and antiinflammatory activities in formalin-induced pain in mice and carrageenan-induced paw edema model in rat.

6-phenyltetrahydro-1,3-oxazin-2-one derivative and pharmaceutical composition containing the same

-

, (2008/06/13)

A 6-phenyltetrahydro-1,3-oxazin-2-one derivative having the formula (I): wherein, R1is an unsubstituted or substituted C1to C8alkyl group; an unsubstituted or substituted C3to C7cycloalkyl group;, etc

COMPOUNDS CONTAINING PHENYL LINKED TO ARYL OR HETEROARYL BY AN ALIPHATIC- OR HETEROATOM-CONTAINING LINKING GROUP

-

, (2008/06/13)

This invention is directed to the pharmaceutical use of phenyl compounds, which are linked to an aryl moiety by various linkages, for inhibiting tumor necrosis factor. The invention is also directed to the compounds, their preparation and pharmaceutical compositions containing these compounds. Furthermore, this invention is directed to the pharmaceutical use of the compounds for inhibiting cyclic AMP phosphodiesterase

Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic-or heteroatom-containing linking group

-

, (2008/06/13)

This invention is directed to the pharmaceutical use of phenyl compounds, which are linked to an aryl moiety by various linkages, for inhibiting tumor necrosis factor. The invention is also directed to the compounds, their preparation and pharmaceutical compositions containing these compounds. Furthermore, this invention is directed to the pharmaceutical use of the compounds for inhibiting cyclic AMP phosphodiesterase.

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