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152630-47-2

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152630-47-2 Usage

Complex structure

The compound has a complex structure that includes a cyclopentyl group, a methoxyphenyl group, and a carbonitrile functional group.

Six-membered ring

The compound contains a six-membered ring with a carbonyl group and a nitrile group attached.

Phenyl ring

The compound also contains a phenyl ring that is substituted with a methoxy group and a cyclopentyloxy group.

Potential applications

The presence of these functional groups and rings suggests that this compound may have potential applications in pharmaceuticals, materials science, or other industries.

Further research needed

Further research and analysis would be needed to fully understand the properties and potential uses of this chemical.

Molecular weight

The molecular weight of the compound is approximately 315.4 g/mol.

Appearance

The compound is likely to be a solid at room temperature, although further analysis would be needed to confirm this.

Solubility

The solubility of the compound in various solvents is not known and would require further analysis.

Stability

The stability of the compound under different conditions, such as temperature, pressure, and exposure to light, is not known and would require further analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 152630-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,6,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 152630-47:
(8*1)+(7*5)+(6*2)+(5*6)+(4*3)+(3*0)+(2*4)+(1*7)=112
112 % 10 = 2
So 152630-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H23NO3/c1-22-17-7-6-14(12-18(17)23-16-4-2-3-5-16)19(13-20)10-8-15(21)9-11-19/h6-7,12,16H,2-5,8-11H2,1H3

152630-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-cyclopentyloxy-4-methoxyphenyl)-4-oxocyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:152630-47-2 SDS

152630-47-2Relevant articles and documents

CONDENSED HETEROCYCLIC COMPOUNDS AS PDE-IV INHIBITORS FOR THE TREATMENT OF INFLAMMATORY AND ALLERGIC DISORDERS

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Page 44, (2010/11/30)

The present invention relates to novel heterocyclic compounds that inhibit phosphodiesterase type 4 (PDE4). The compounds are useful for treating inflammatory conditions, diseases of the central nervous system and insulin resistant diabetes , (formula I)

Compounds and method for preparing substituted 4-phenyl-4-cyanocyclohexanoic acids

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Example 6, (2008/06/13)

This invention relates to a method of preparing a compound of the following type by treating a compound of formula (II) with lithium bromide, magnesium bromide and the like.

1,4-Cyclohexanecarboxylates: Potent and selective inhibitors of phosophodiesterase 4 for the treatment of asthma

Christensen, Siegfried B.,Guider, Aimee,Forster, Cornelia J.,Gleason, John G.,Bender, Paul E.,Karpinski, Joseph M.,Dewolf Jr., Walter E.,Barnette, Mary S.,Underwood, David C.,Griswold, Don E.,Cieslinski, Lenora B.,Burman, Miriam,Bochnowicz, Steven,Osborn, Ruth R.,Manning, Carol D.,Grous, Marilyn,Hillegas, Leonard M.,Bartus, Joan O'Leary,Dominic Ryan,Eggleston, Drake S.,Curtis Haltiwanger,Torphy, Theodore J.

, p. 821 - 835 (2007/10/03)

Evaluation of a variety of PDE4 inhibitors in a series of cellular and in vivo assays suggested a strategy to improve the therapeutic index of PDE4 inhibitors by increasing their selectivity for the ability to inhibit PDE4 catalytic activity versus the ability to compete for high affinity [3H]rolipram-binding sites in the central nervous system. Use of this strategy led ultimately to the identification of cis-4-cyano-4-[3- (cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxylic acid (1, SB 207499, Ariflo(TM)), a potent second-generation inhibitor of PDE4 with a decreased potential for side effects versus the archetypic first generation inhibitor, (R)-rolipram.

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