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2,5-Dicyclopentyl cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77189-09-4

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77189-09-4 Usage

Structure

Cyclic ketone with two cyclopentyl groups attached to a central cyclopentanone ring

Uses

Production of flavor and fragrance compounds, intermediate in synthesis of pharmaceuticals and other organic compounds

Potential applications

Organic synthesis, materials science
Versatile and valuable compound with wide range of potential uses in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 77189-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,8 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77189-09:
(7*7)+(6*7)+(5*1)+(4*8)+(3*9)+(2*0)+(1*9)=164
164 % 10 = 4
So 77189-09-4 is a valid CAS Registry Number.

77189-09-4SDS

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 2,5-dicyclopentylcyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2,5-Dicyclopentylcyclopentanone

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:77189-09-4 SDS

77189-09-4Upstream product

77189-09-4Relevant academic research and scientific papers

Reductive dimerization and oligomerization of alcohols, ketones, and aldehydes to hydrocarbons on a promoted, fused iron catalyst

Glebov,Zaikin,Mikaya,Kliger

, p. 296 - 308 (2014/08/05)

A new reductive dimerization and oligomerization reaction of (C5 and C6) cycloalkanols and cycloalkanones, benzaldehyde, and benzyl alcohol to hydrocarbons containing as many, or more, carbon atoms as the reactant oxygenated compound on a promoted, fused iron catalyst proceeds at a temperature of 250-350°C, a hydrogen pressure of 0.1-1 MPa, a specific feed rate of oxygenated reagent of 80-320 g h-1kg-1Ct, and a hydrogen space velocity of 1 × 103 to 20 × 103 h-1. Possible reaction mechanisms have been considered.

New one-pot multistep process with multifunctional catalysts: Decreasing the e factor in the synthesis of fine chemicals

Climent, Maria J.,Corma, Avelino,Iborra, Sara,Mifsud, Maria,Velty, Alexandra

experimental part, p. 99 - 107 (2010/05/18)

The synthesis of a series of fine chemicals (4-(4-methoxyphenyl)-2- butanone, 4-(6,6-dimethylbicyclo[3,1,1]hept-2-en-2-yl)-2-butanone, and 2-cyclopentylcylopentanone) has been performed through a simple process that involves one-pot multi-step reactions (condensation-dehydration-reduction) using multifunctional base-acid-metal catalysts. The E factor for the specific process, as well as for the global process that includes the manufacturing of the reactants, has been calculated and compared with those obtained using conventional methods. In various cases, it is demonstrated that by means of process intensification with multifunctional solid catalysts, it is possible to decrease the E factor by one order of magnitude or more with respect to any of the manufacturing routes reported to date.

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