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3-Oxo-1-phenylcyclopentanecarbonitrile is a chemical compound with the molecular formula C13H11NO. It is a derivative of cyclopentane, a five-membered cyclic hydrocarbon, with a phenyl group attached to the first carbon atom. The compound features a carbonitrile group (-CN) at the end of the cyclopentane ring and a ketone group (C=O) at the third carbon atom. This organic compound is known for its unique structure and properties, making it a subject of interest in various chemical research and applications. Due to its complex structure, 3-oxo-1-phenylcyclopentanecarbonitrile can be used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.

84409-26-7

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84409-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84409-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,0 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84409-26:
(7*8)+(6*4)+(5*4)+(4*0)+(3*9)+(2*2)+(1*6)=137
137 % 10 = 7
So 84409-26-7 is a valid CAS Registry Number.

84409-26-7SDS

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 3-Oxo-1-phenyl-cyclopentanecarbonitrile

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

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More Details:84409-26-7 SDS

84409-26-7Downstream Products

84409-26-7Relevant academic research and scientific papers

CHEMOSELECTIVE METHYLENE HYDROXYLATION IN AROMATIC MOLECULES

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Paragraph 0230; 0235-0236, (2020/03/28)

A chemoselective and reactive Mn(CF3-PDP) catalyst system that enables for the first time the strategic advantages of late-stage aliphatic C—H hydroxylation to be leveraged in aromatic compounds. This discovery will benefit small molecule therapeutics by enabling the rapid diversification of aromatic drugs and natural products and identification of their metabolites.

Chemoselective methylene oxidation in aromatic molecules

Zhao, Jinpeng,Nanjo, Takeshi,de Lucca, Emilio C.,White, M. Christina

, p. 213 - 221 (2019/01/04)

Despite significant progress in the development of site-selective aliphatic C–H oxidations over the past decade, the ability to oxidize strong methylene C–H bonds in the presence of more oxidatively labile aromatic functionalities remains a major unsolved

SYNTHESIS AND PROPERTIES OF 1-ARYL-3-OXO-1-CYCLOPENTANECARBOXYLIC ACIDS AND THEIR DERIVATIVES

Mndzhoyan, Sh.L.,Martirosyan, A.O.,Ovakimyan, A.R.

, p. 1648 - 1651 (2007/10/02)

A synthesis was developed for 1-phenyl- and 1-(alkoxyphenyl)-3-oxo-1-cyclopentanecarboxylic acids, and some of their derivatives were obtained.

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