20073-50-1

Basic information

• Product Name: 2-(3-OXAZOLIDINE)ETHANOL
• Synonyms: 3-oxazolidineethanol;2-(3-OXAZOLIDINE)ETHANOL;N-(2-HYDROXYETHYL)OXAZOLIDINE;TIMTEC-BB SBB008304;oxazolidine-3-ethanol;Einecs 243-499-2
• CAS NO: 20073-50-1
• Molecular Formula: C₅H₁₁NO₂
• Molecular Weight: 117.15
• EINECS: 243-499-2
• Mol File: 20073-50-1.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 206.8°Cat760mmHg
• Flash Point: 78.8°C
• Appearance: /
• Density: 1.106g/cm³
• Vapor Pressure: 0.0549mmHg at 25°C
• Refractive Index: 1.475
• Water Solubility: 1000g/L at 25℃
• CAS DataBase Reference: 2-(3-OXAZOLIDINE)ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-OXAZOLIDINE)ETHANOL(20073-50-1)
• EPA Substance Registry System: 2-(3-OXAZOLIDINE)ETHANOL(20073-50-1)

Safety Data

• Hazardous Substances Data: 20073-50-1(Hazardous Substances Data)

Usage

General Description

2-(3-OXAZOLIDINE)ETHANOL is a chemical compound with the molecular formula C5H11NO2. It is a derivative of oxazolidine, a five-membered heterocyclic ring that contains both nitrogen and oxygen atoms. 2-(3-OXAZOLIDINE)ETHANOL is often used as a building block in the synthesis of organic compounds and pharmaceuticals. It is also used as a chelating agent in metal ion removal and as a reagent in organic chemistry reactions. 2-(3-OXAZOLIDINE)ETHANOL has potential applications in various industries including pharmaceuticals, agrochemicals, and materials science due to its versatile reactivity and functional groups. It is important to handle this chemical with care and according to safety protocols, as it may pose hazards if mishandled.

InChI:InChI=1/C5H11NO2/c7-3-1-6-2-4-8-5-6/h7H,1-5H2

Upstream product

• 50-00-0 formaldehyd 
• 111-42-2 2,2'-iminobis[ethanol] 
• 590-86-3 isovaleraldehyde 
• 71-36-3 butan-1-ol 

Downstream Products

• 1424252-24-3 C₄₆H₇₁NO₇ 
• 1424252-22-1 C₄₆H₇₁NO₇ 
• 1424252-16-3 C₃₀H₅₅NO₅ 
• 1424252-14-1 C₃₀H₅₅NO₅ 
• 1424252-10-7 C₂₆H₄₇NO₃ 
• 1424252-12-9 C₂₆H₄₇NO₃ 
• 99614-02-5 ondanserton 
• 120635-47-4 4,5,6,8,9,10-hexahydro-10-[(2-methyl-1H-imidazol-1-yl)methyl]-11H-pyrido-[3,2,1-jk]-carbazol-11-one 
• 154198-23-9 2-<(bis-2-hydroxyethyl)aminomethyl>-3,5-dimethoxy-6-formylphenol 
• 105892-13-5 (4-Chloro-phenylsulfanyl)-acetic acid; compound with 2-oxazolidin-3-yl-ethanol 
• 17816-81-8 1-benzoyloxy-2-oxazolidin-3-yl-ethane 
• 105-59-9 N-Methyldiethanolamine 
• 86241-19-2 2-(bis(2-hydroxyethyl)amino)acetonitrile 
• 1462469-84-6 (E)-6-(2-(3-oxazolidinyl)ethoxy)-2-(4-dimethylaminostyryl)benzofuran 

Relevant articles and documents

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Aldehydes containing hydroxl groups

The present invention relates to aldehydes of the formula (I) which contain tertiary amino groups and at least one hydroxyl group. Aldehydes of this kind can be utilized broadly. Aldehydes of particular advantage can be incorporated into a polymer, and find use as curing agents and/or catalysts. Preferably they find use in adhesives and sealants.

PREPARATION OF DELMOPINOL

It comprises a process for the production of delmopinol or a pharmaceutically acceptable salt and/or a solvate thereof, by subjecting the compound of formula (II) where R1 and R2 are the same or different, independently selected from the group consisting of H, (C1-C6) alkyl or, alternatively, R1 and R2 form, together with the carbon atom to which they are attached, a (C5-C6) cycloalkyl radical; and R3 is a radical selected from the group consisting of CF3, (C1-C4) alkyl, phenyl, and phenyl mono- ordisubstituted by a radical selected from the group consisting of (C1-C4)-alkyl, halogen and nitro to a deprotection and cyclisation reaction. The process is useful to prepare delmopinol or its salts on an industrial scale. The compound of formula (II) is new and also forms part of the present invention, as well as its preparation process and other new intermediates of said preparation process. .