32444-34-1

Usage

Uses

Used in Chemical Industry:
1-Butanol, 2-ethyl-3-methylis used as a solvent in the chemical industry for the production of plastics, resins, and coatings. Its solubility in organic solvents makes it an ideal component in these processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Butanol, 2-ethyl-3-methylserves as a precursor for the manufacture of other chemicals, which are then used in the development of various medications. Its versatility in chemical reactions contributes to its importance in this field.
Used in Cosmetic Industry:
1-Butanol, 2-ethyl-3-methylalso finds applications in the cosmetic industry, where it is used as a component in the formulation of various cosmetic products. Its properties allow it to enhance the performance and stability of these products.
Used as a Precursor for Chemical Synthesis:
1-Butanol, 2-ethyl-3-methylis used as a precursor for the synthesis of other chemicals, such as butyl acetate and butyl glycol. These derived chemicals have their own specific applications in various industries, further expanding the utility of 1-Butanol, 2-ethyl-3-methyl-.
Safety Precautions:
It is crucial to handle 1-Butanol, 2-ethyl-3-methylwith care, as it can be harmful if inhaled, ingested, or comes into contact with the skin. Proper safety measures should be taken during its use to minimize potential health risks.

InChI:InChI=1/C7H16O/c1-4-7(5-8)6(2)3/h6-8H,4-5H2,1-3H3

Upstream product

• 128399-50-8 3-chloromethyl-2-methylpentane 
• 41178-79-4 2-methyl-3-hydroxymethyl-pentene-⁽³⁾ 
• 63791-85-5 2-Ethyl-3-methylbutansaeure-ethylester 
• 24910-63-2 2,3-dimethyl-pent-2-ene 
• 109929-22-8 1,2,3-(CH₃)3C₃H₂Br 
• 503-74-2 3-methylbutyric acid 
• 2747-53-7 3-methyl-3-penten-2-ol 
• 32444-33-0 methyl 2-ethyl-3-methylbutyrate 
• 1522-46-9 ethyl 2-isopropylacetoacetate 
• 56006-49-6 2-ethyl-3-methyl-butyric acid 

Downstream Products

• 55504-75-1 (2-Ethyl-3-methyl-butoxysulfonyl)-phenyl-acetic acid 
• 170511-91-8 2-ethyl-3-methylbutyl phenyl sulphone 
• 170511-90-7 2-ethyl-3-methylbutyl phenyl sulfide 
• 92372-38-8 2-ethyl-3-methyl-1-(p-tolylsulfonyloxy)butane 

Relevant academic research and scientific papers

Syntheses and evaluation of anticonvulsant activity of novel branched alkyl carbamates

A novel class of 19 carbamates was synthesized, and their anticonvulsant activity was comparatively evaluated in the rat maximal electroshock (MES) and subcutaneous metrazol (scMet) seizure tests and pilocarpine-induced status epilepticus (SE) model. In spite of the alkyl-carbamates' close structural features, only compounds 34, 38, and 40 were active at the MES test. The analogues 2-ethyl-3-methyl-butyl-carbamate (34) and 2-ethyl-3-methyl-pentyl- carbamate (38) also exhibited potent activity in the pilocarpine-SE model 30 min postseizure onset. Extending the aliphatic side chains of homologous carbamates from 7 to 8 (34 to 35) and from 8 to 9 carbons in the homologues 38 and 43 decreased the activity in the pilocarpine-SE model from ED50 = 81 mg/kg (34) to 94 mg/kg (35) and from 96 mg/kg (38) to 114 mg/kg (43), respectively. The most potent carbamate, phenyl-ethyl-carbamate (47) (MES ED50 = 16 mg/kg) contains an aromatic moiety in its structure. Compounds 34, 38, 40, and 47 offer the optimal efficacy-safety profile and, consequently, are promising candidates for development as new antiepileptics.

SYNTHESIS OF (24R)-HOMOBRASSINOLIDE

The synthesis from stigmasterol of C-29 brassinosteroids containing an (R)-ethyl group at C24 - (24R)-homocastasterone and (24R)-homobrassinolide - is described.The structure of the carbon skeleton of the side-chain was achieved by condensing a C-22 aldeh

SYNTHESIS OF SOME NEW CHOLESTERYL ESTERS OF CHIRAL ALKANOIC ACIDS.

Six new cholesteryl esters have been prepared from chiral alkanoic acids. Oxidation of 2(S)-methylbutanol and 2(S)-ethyl-3-methybutyraldehyde gave the corresponding butyric acids, while condensation of the tosylates of the corresponding alcohols with diethyl malonate led ultimately to the substituted hexanoic acids. 2(R)-Methylpentanoic and ( minus )-2-ethylhexanoic acids were commercially available.