5345-01-7

Usage

Uses

Used in Pharmaceutical Industry:
3-Ethyl-3-methylglutaric acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drug molecules, enhancing the therapeutic potential of existing medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Ethyl-3-methylglutaric acid is utilized as a precursor in the production of agrochemicals, playing a crucial role in the creation of effective and environmentally friendly pest control agents.
Used in Flavors and Fragrances Industry:
3-Ethyl-3-methylglutaric acid is employed as a precursor in the synthesis of flavors and fragrances, contributing to the development of unique and complex scents and tastes for various consumer products.
Used in Organic Synthesis and Chemical Research:
3-Ethyl-3-methylglutaric acid is used as a valuable compound in organic synthesis and chemical research, enabling the exploration of new chemical reactions and the discovery of innovative applications in various fields.

InChI:InChI=1/C8H14O4/c1-3-8(2,4-6(9)10)5-7(11)12/h3-5H2,1-2H3,(H,9,10)(H,11,12)/p-2

Upstream product

• 1197-86-0 2-methyl-5-ethyl-5-methylcyclohexane-1,3-dione 
• 1135-62-2 4-ethyl-4-methyl-3,5-dicyano-2,6-piperidinedione 
• 7664-93-9 sulfuric acid 
• 872821-77-7 4-ethyl-5-cyano-2-imino-4-methyl-6-oxo-piperidine-3-carboxylic acid amide 
• 872821-88-0 9-ethyl-4,8-diamino-9-methyl-3,7-diaza-bicyclo[3.3.1]nona-3,7-diene-2,6-dione 
• 90961-79-8 9-ethyl-9-methyl-3,7-diaza-bicyclo[3.3.1]nonane-2,4,6,8-tetraone 
• 15025-17-9 4-ethyl-4-methyl-tetrahydro-pyran-2-one 

Downstream Products

• 50849-40-6 N,β-Dimethyl-β-ethyl-glutarimid 
• 102165-68-4 4-ethyl-1-[5-(4-amino-phenoxy)-pentyl]-4-methyl-piperidine-2,6-dione 
• 6970-57-6 3-ethyl-3-methylglutaric anhydride 
• 64-65-3 bemegride 
• 1197-86-0 2-methyl-5-ethyl-5-methylcyclohexane-1,3-dione 
• 4045-31-2 4-ethyl-4-methylpiperidine 
• 5338-98-7 3-ethyl-3-methyl-glutaric acid monomethyl ester 

Relevant academic research and scientific papers

1,1-Alkanediol dicarboxylate linked antibacterial agents

Useful antibacterial agents in which a penicillin and/or a beta-lactamase inhibitor are linked via 1,1-alkanediol dicarboxylates are of the formula STR1 where A is the residue of certain dicarboxyic acids, R3 is H or (C1 -C3), n is zero or 1 such that when n is zero R is P or B and R1 is the residue of certain esters, H or a salt thereof; and when n is 1, one of R and R1 is P and the other is B, and P is STR2 where R2 is H or certain acyl groups, and B is the residue of a beta-lactamase inhibiting carboxylic acid; a method for their use, pharmaceutical compositions thereof and intermediates useful in their production.

Bis-esters of dicarboxylic acids with amoxicillin and certain hydroxymethylpenicillanate 1,1-dioxides

Antibacterial bis-esters of 1,4-cyclohexanedicarboxylic acids and alkane dicarboxylic acids wherein the ester moieties are derived from different alcohols; one alcohol being hydroxymethylpenicillanate 1,1-dioxide, or the 6-beta-hydroxymethyl or the 6-alpha-aminomethyl derivative thereof; and the other being 6-[D-(2-amino-2-(p-hydroxyphenyl)acetamido)]penicillanic acid (amoxicillin); and pharmaceutically acceptable salts thereof; a method for the use of said esters and their salts, and methods for their preparation.

Geminate-Substituted Cyclopentadienes. 1. Synthesis of 5,5-Dialkylcyclopentadienes via 4,4-Dialkylcyclopent-2-en-1-ones.

A synthetic route for the preparation of 5,5,-dialkylcyclopentadienes (1) via 4,4-dialkylcyclopent-2-en-1-ones (3) is described.Beginnig with ketones (in which the two carbonyl substituents will become the two alkyl groups in the title compounds), the route traverses the Guareschi imides 5, 3,3-dialkylglutaric acids 4 and their ethyl esters 7, masked acyloins 8, cyclopentenones 3, alkohols 9, and bromides 10 to reach the dienes 1.Physical properties of five such derivates 1 and 3 (dimethyl, methylethyl,diethyl, methyl-n-propyl, and methylisopropyl) are presented.