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2-Methylpimelic acid dimethyl ester is an organic compound that belongs to the class of dicarboxylic acids and derivatives. It is characterized by the presence of two carboxylic acid groups. 2-Methylpimelic acid dimethyl ester is often utilized in research studies as a reagent. With a molecular formula of C10H16O4 and a molar mass of 200.227 g/mol, it typically appears as a white crystalline powder and has a relatively low melting point. Due to its potential to cause eye and skin irritation, it requires careful handling.

33658-48-9

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33658-48-9 Usage

Uses

Used in Scientific Research:
2-Methylpimelic acid dimethyl ester is used as a reagent in various research studies for its unique chemical properties and potential applications in the development of new compounds and materials.
Used in Industrial Applications:
2-Methylpimelic acid dimethyl ester is used as a chemical intermediate in the synthesis of other organic compounds, contributing to the production of various industrial products.
Used in Pharmaceutical Development:
2-Methylpimelic acid dimethyl ester is used as a starting material in the development of pharmaceuticals, potentially leading to the creation of new drugs and therapeutic agents.
Used in Chemical Synthesis:
2-Methylpimelic acid dimethyl ester is used as a building block in the synthesis of complex organic molecules, playing a crucial role in the advancement of organic chemistry and its applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 33658-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,5 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33658-48:
(7*3)+(6*3)+(5*6)+(4*5)+(3*8)+(2*4)+(1*8)=129
129 % 10 = 9
So 33658-48-9 is a valid CAS Registry Number.

33658-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 2-methylheptanedioate

1.2 Other means of identification

Product number -
Other names Dimethyl 2-methylheptane-1,7-dioate

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:33658-48-9 SDS

33658-48-9Relevant academic research and scientific papers

Reactivity of 1,3-dimethylimidazolium-2-carboxylate with dimethylcarbonate at high temperature: Unexpected 2-ethyl-functionalisation of the imidazolium moiety and employment of the NHC-CO2/dimethylcarbonate system in a base promoted reaction

Annese, Cosimo,D'Accolti, Lucia,Fusco, Caterina,Tommasi, Immacolata

, p. 94 - 97 (2014/01/17)

The reaction of 1,3-dimethylimidazolium-2-carboxylate and dimethylcarbonate (DMC) at high temperature yielded the new compounds 2-ethyl-1,3- dimethylimidazolium methyl carbonate salt and 2-ethyl-1,3-dimethylimidazolium-4- carboxylate zwitterion which were obtained as a mixture in approximately 4:1 molar ratio. The compounds were also isolated in pure form through alternative synthetic procedures and characterized by ESI-HRMS, 1H, 13C NMR and FTIR spectroscopy. The 1,3-dimethylimidazolium-2- carboxylate/dimethylcarbonate system was employed in the synthesis of 1,7-heptanedioic acid dimethyl ester from cyclohexanone and DMC. The target compound was obtained in 49% yield and 66% selectivity.

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