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"Benzene, (2-cyclopentylethyl)-" is a chemical compound with the molecular formula C13H18. It is an aromatic hydrocarbon, characterized by a benzene ring with a 2-cyclopentylethyl side chain attached to it. Benzene, (2-cyclopentylethyl)- is also known as 1-phenylcyclopentane or cyclopentylbenzene. It is a colorless liquid with a density of 0.93 g/cm3 and a boiling point of 247-248°C. The compound is insoluble in water but soluble in organic solvents. It is used in the synthesis of various organic compounds and as a chemical intermediate in the pharmaceutical and chemical industries. Due to its potential health risks, it is important to handle Benzene, (2-cyclopentylethyl)- with proper safety measures.

4413-19-8

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4413-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4413-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4413-19:
(6*4)+(5*4)+(4*1)+(3*3)+(2*1)+(1*9)=68
68 % 10 = 8
So 4413-19-8 is a valid CAS Registry Number.

4413-19-8SDS

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 (2-cyclopentylethyl)benzene

1.2 Other means of identification

Product number -
Other names 2-Phenylethyl-cyclopentan

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:4413-19-8 SDS

4413-19-8Relevant academic research and scientific papers

From Dimethylamine to Pyrrolidine: The Development of an Improved Nickel Pincer Complex for Cross-Coupling of Nonactivated Secondary Alkyl Halides

Perez Garcia, Pablo M.,Di Franco, Thomas,Epenoy, Alexandre,Scopelliti, Rosario,Hu, Xile

, p. 258 - 261 (2016/01/12)

Replacement of a dimethyl amino group of the amidobis(amine) nickel(II) pincer complex (1), [(MeN2N)Ni-Cl], by a pyrrolidino group resulted in a new nickel(II) pincer complex (2), [(PyrNMeNN)Ni-Cl]. Complex 2 is an efficient catalyst for Kumada and Suzuki-Miyaura cross-coupling of nonactivated secondary alkyl halides, while complex 1 is largely inactive. The significant activity difference is tentatively attributed to a minimal structural difference, which leads to a more hemilabile ligand.

Tandem intramolecular carbolithiation-lithium/zinc transmetallation and applications to carbon-carbon bond-forming reactions

Yus, Miguel,Ortiz, Rosa

, p. 3833 - 3841 (2007/10/03)

Lithium/zinc transmetallation with the cyclic organolithium intermediate 3 (prepared by intramolecular carbolithiation of the initially formed organolithium 2) gives the corresponding organozinc intermediate 5. Copper- or palladium-promoted SN2

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