Welcome to LookChem.com Sign In|Join Free
  • or
Cyclopentyl hexanoate is an organic compound with the chemical formula C11H20O2. It is a colorless to pale yellow liquid with a fruity, peach-like odor. This ester is formed by the reaction of cyclopentyl alcohol and hexanoic acid, and it is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. Cyclopentyl hexanoate is known for its ability to provide a fresh, fruity scent and is often used in combination with other fragrance compounds to create complex and appealing aromas. It is considered safe for use in cosmetics and has been approved by the International Fragrance Association (IFRA).

5413-59-2

Post Buying Request

5413-59-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5413-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5413-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5413-59:
(6*5)+(5*4)+(4*1)+(3*3)+(2*5)+(1*9)=82
82 % 10 = 2
So 5413-59-2 is a valid CAS Registry Number.

5413-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopentyl hexanoate

1.2 Other means of identification

Product number -
Other names hexanoic acid cyclopentyl ester

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:5413-59-2 SDS

5413-59-2Downstream Products

5413-59-2Relevant academic research and scientific papers

Ruthenium pincer-catalyzed cross-dehydrogenative coupling of primary alcohols with secondary alcohols under neutral conditions

Srimani, Dipankar,Balaraman, Ekambaram,Gnanaprakasam, Boopathy,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 2403 - 2406 (2012/11/07)

Cross-dehydrogenative coupling of primary alcohols with secondary alcohols to obtain mixed esters with the liberation of molecular hydrogen is achieved in high yield and good selectivity under neutral conditions, using a bipyridyl-based PNN ruthenium(II) pincer catalyst. Copyright

Ruthenium pincer-catalyzed acylation of alcohols using esters with liberation of hydrogen under neutral conditions

Gnanaprakasam, Boopathy,Ben-David, Yehoshoa,Milstein, David

supporting information; experimental part, p. 3169 - 3173 (2011/02/23)

Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex. Copyright

A simple and convenient one-pot synthesis of fatty acid esters from hindered alcohols using N,N-dimethylchloro-sulfitemethaniminium chloride as dehydrating agent

Kaul, Savita,Kumar, Ajay,Sain, Bir,Gupta

, p. 2885 - 2891 (2007/10/03)

N,N-Dimethylchlorosulfitemethaniminium chloride (SOCl2-DMF) has been found to be an efficient reagent for one-pot synthesis of esters from equimolar amounts of fatty acids and hindered alcohols under mild conditions.

Synthesis and Bioevaluation of Alicyclic and Heterocyclic Alkanoates as Cockroach Attractants

Pandey, Karuna Shanker,Mendki, Murlidhar Jaywantrao,Rao, Karumuru Mallikarjuna,Vaidyanathaswamy, Ramamoorthy

, p. 725 - 727 (2007/10/02)

A series of homo and heterocyclic alkanoates were prepared and evaluated as insect attractants toward Blattella germanica (L.) and Supella longipalpa (F.).Among these compounds, the tetrahydrofurfuryl alkanoates and 4-tetrahydropyranyl hexanoate showed relatively better activity.It was also observed that, in general, the five-membered compounds were better performers than their six-membered counterparts.The introdiction of an oxygen atom in the ring enhanced the activity, irrespective of the ring size.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5413-59-2