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Pentanoic acid, cyclopentyl ester (9CI), also known as cyclopentyl valerate, is an organic compound with the chemical formula C10H18O2. It is an ester derived from pentanoic acid (valeric acid) and cyclopentyl alcohol. This colorless liquid has a fruity, apple-like odor and is used in the fragrance industry as a flavoring agent and perfume ingredient. It is characterized by its ability to add depth and richness to various scents, particularly in the creation of fruity, floral, and green notes. The compound is also known for its low toxicity and is generally recognized as safe for use in cosmetics and food products.

5451-99-0

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5451-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5451-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5451-99:
(6*5)+(5*4)+(4*5)+(3*1)+(2*9)+(1*9)=100
100 % 10 = 0
So 5451-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-2-3-8-10(11)12-9-6-4-5-7-9/h9H,2-8H2,1H3

5451-99-0SDS

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 cyclopentyl pentanoate

1.2 Other means of identification

Product number -
Other names Pentanoic 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:5451-99-0 SDS

5451-99-0Downstream Products

5451-99-0Relevant academic research and scientific papers

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

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.

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