28562-61-0

Basic information

• Product Name: 3-Ethyloxetane-3-carboxyl...
• Synonyms: 3-Ethyloxetane-3-carboxyl...;3-ETHYLOXETANE-3-CARBOXYLIC ACID;3-Carboxyl-3-ethyloxetane;3-Ethyl-3-oxetanecarboxylic acid;3-ETHYLOXETANE-3-CARBOXYLIC
• CAS NO: 28562-61-0
• Molecular Formula: C₆H₁₀O₃
• Molecular Weight: 130.1418
• Mol File: 28562-61-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 25℃
• Boiling Point: 237℃
• Flash Point: 100℃
• Appearance: /
• Density: 1.180
• PKA: 3.94±0.20(Predicted)
• CAS DataBase Reference: 3-Ethyloxetane-3-carboxyl...(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethyloxetane-3-carboxyl...(28562-61-0)
• EPA Substance Registry System: 3-Ethyloxetane-3-carboxyl...(28562-61-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 28562-61-0(Hazardous Substances Data)

Usage

General Description

3-Ethyloxetane-3-carboxyl is a chemical compound that belongs to the oxetane family. It is also known as 3-ethyloxetane-3-carboxylic acid and has the molecular formula C6H10O3. 3-Ethyloxetane-3-carboxyl... is a colorless liquid with a boiling point of approximately 137-139°C. It is used in various chemical processes and has the potential to be a building block for the synthesis of other organic compounds. Additionally, it has been studied for its potential use in medicinal and pharmaceutical applications.

Upstream product

• 3047-32-3 3-ethyl-3-(hydroxymethyl)oxetane 

Downstream Products

• 1365969-56-7 benzyl N-(3-ethyloxetan-3-yl)carbamate 
• 1572510-65-6 C₁₉H₂₁FN₂O₄S 

Relevant articles and documents

Synthesis and property of novel amino acid-based polymers by self-polyaddition of monomers containing both oxetanyl and carboxyl groups

A new synthetic strategy for polymers containing amino acids in the main chain was developed. Monomers N-oxetanylalanine (N-Oxe-Ala-COOH), N-oxetanylglutamic acid (N-Oxe-Glu-COOH), and N-oxetanyllysine (N-Oxe-Lys-COOH) containing both oxetanyl and carboxyl groups were synthesized, and self-polyaddition and self-copolyaddition of these monomers afforded the corresponding polymers containing amino acids in the main chain [poly( OxAla), poly(OxLys), poly(OxGlu), poly( OxAla-co-OxGlu), poly(OxGlu-co- OxLys), and poly(OxAla-co-OxLys)] with molecular weight in the range of 920-6620, in satisfactory yields. The physical properties, such as solubility, glass transition temperature, and thermal stability, were consistent with the amount of carboxyl groups at the chain ends. Biodegradability of the polymers was examined by the biochemical oxygen demand method; the decomposition ratios of poly(OxAla) and poly( OxAla-co-OxGlu) were about 60%, whereas that of poly( OxGlu) was nearly 100% after 28 days. 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 This article reports the development of new strategy for polymers containing amino acids in the main chain. Monomers containing both oxetanyl and carboxyl groups were synthesized derived from amino acids, and self-polyaddition and self-copolyaddition of these monomers afforded the corresponding polymers containing amino acids in the main chain. The obtained amino -acid- based polymers had good solubility, high- glass transition temperature, high thermal stability, and good biodegradability. Copyright

Process for the preparation of 2,2-bis-chloro-methylalkanecarboxylic acid chlorides

A process for the preparation of a 2,2-bis-chloro-methyl-alkanecarboxylic acid of the formula STR1 in which R is hydrogen, alkyl, cycloalkyl or optionally substituted phenyl, which comprises reacting an oxetane-3-carboxylic acid of the formula STR2 or a salt thereof, with an inorganic acid chloride at a temperature between 20° C. and the boiling point of the reaction mixture. The products are known intermediates for fungicides and herbicides.