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Dimethyl cyclopentylmalonate is a colorless liquid chemical compound with the molecular formula C9H14O4, characterized by a fruity odor and a sweet, fruity, pineapple-like aroma and flavor. It is commonly utilized as a flavoring agent in the food and beverage industry, as well as in the production of pharmaceuticals and fragrances. Recognized for its safety, it is approved for use by regulatory bodies such as the Food and Drug Administration (FDA) in the United States.

82491-60-9

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82491-60-9 Usage

Uses

Used in Food and Beverage Industry:
Dimethyl cyclopentylmalonate is used as a flavoring agent for its ability to impart a sweet, fruity, and pineapple-like aroma and flavor to various food and beverage products, enhancing their taste and appeal to consumers.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Dimethyl cyclopentylmalonate serves as a key component in the development of medications, contributing to the overall formulation and effectiveness of certain drugs.
Used in Fragrance Industry:
Dimethyl cyclopentylmalonate is also utilized in the fragrance industry, where it adds a fruity scent to perfumes, colognes, and other scented products, providing a pleasant and attractive aroma.

Check Digit Verification of cas no

The CAS Registry Mumber 82491-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,9 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82491-60:
(7*8)+(6*2)+(5*4)+(4*9)+(3*1)+(2*6)+(1*0)=139
139 % 10 = 9
So 82491-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O4/c1-13-9(11)8(10(12)14-2)7-5-3-4-6-7/h7-8H,3-6H2,1-2H3

82491-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl Cyclopentylmalonate

1.2 Other means of identification

Product number -
Other names dimethyl 2-cyclopentylpropanedioate

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:82491-60-9 SDS

82491-60-9Relevant academic research and scientific papers

INHIBITORS OF HISTONE DEACETYLASE

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Paragraph 0302, (2016/04/26)

This invention provides compounds that are inhibitors of HDAC2. The compounds (e.g., compounds according to Formula (I), (II), (IIa), (III), (IV), (V), or (VI)) accordingly are useful for treating, alleviating, or preventing a condition in a subject such as a neurological disorder, memory or cognitive function disorder or impairment, extinction learning disorder, fungal disease or infection, inflammatory disease, hematological disease, or neoplastic disease, or for improving memory or treating, alleviating, or preventing memory loss or impairment.

Electrochemical Cyclodimerization of Alkylidenemalonates

Elinson, Michail N.,Feducovich, Sergey K.,Zakharenkov, Alexandre A.,Ugrak, Bogdan I.,Nikishin, Gennady I.,et al.

, p. 5035 - 5046 (2007/10/02)

Electrolysis of dimethyl alkylidenemalonates RCH=C(COOMe)2 (R=n-Alk, Ph) in an undivided cell in MeOH in the presence of alkali metal halide as mediator, leads to the formation of cyclic dimers, i.e., 3,4-disubstituted 1,1,2,2-cyclobutanetetracarboxylates.The reaction proceeds via the reductive coupling of two substrate molecules at cathode and the cyclization of a hydrodimer dianion by its interaction with an active form of a mediator, an anode-generated halogen.

ELECTROREDUCTIVE CYCLIZATION. A COMPARISON OF THE ELECTROCHEMICAL AND ANALOGOUS CHEMICAL (MIRC) REACTION

Nugent, Sean T.,Baizer, Manuel M.,Little, R. Daniel

, p. 1339 - 1342 (2007/10/02)

Several examples which illustrate the contrasting and complementary aspects of electroreductive cyclization and MIRC reactions are presented.A brief mechanistic discussion of the electrochemical reaction is given and two examples of the use of an electroc

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