10471-78-0

Basic information

• Product Name: 2-ISOPROPENYL-2-OXAZOLINE 99+%
• Synonyms: 2-ISOPROPENYL-2-OXAZOLINE 99+%;Oxazole, 4,5-dihydro-2-(1-Methylethenyl)-;2-Isopropenyl-4,5-dihydro-oxazole;4,5-dihydro-2-(prop-1-en-2-yl)oxazole
• CAS NO: 10471-78-0
• Molecular Formula: C₆H₉NO
• Molecular Weight: 111.14176
• Product Categories: Monomers;Polymer Science;Vinyl Halides, Amines, Amides, and Other Vinyl Monomers
• Mol File: 10471-78-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: −47 °C(lit.)
• Boiling Point: 147 °C(lit.)
• Flash Point: 119 °F
• Appearance: /
• Density: 1.06 g/mL at 25 °C(lit.)
• Vapor Pressure: 21.4mmHg at 25°C
• Refractive Index: n20/D 1.478(lit.)
• Storage Temp.: 2-8°C
• PKA: 4.45±0.50(Predicted)
• CAS DataBase Reference: 2-ISOPROPENYL-2-OXAZOLINE 99+%(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ISOPROPENYL-2-OXAZOLINE 99+%(10471-78-0)
• EPA Substance Registry System: 2-ISOPROPENYL-2-OXAZOLINE 99+%(10471-78-0)

Safety Data

• Hazard Codes: T
• Statements: 10-23-36/37/38
• Safety Statements: 26-36-45
• RIDADR: UN 3384 6.1/PG 1
• WGK Germany: 3
• Hazardous Substances Data: 10471-78-0(Hazardous Substances Data)

Usage

Uses

2-Isopropenyl-2-oxazoline is used to functionalize polypropylene to be used as compatibilizers for PP/(acrylonitrile-co-butadiene-co-acrylic acid) rubber (NBR) blends.

InChI:InChI=1/C6H9NO/c1-5(2)6-7-3-4-8-6/h1,3-4H2,2H3

Upstream product

• 5238-56-2 N-(2-hydroxyethyl)methacrylamide 
• 18266-55-2 N-(2-hydroxyethyl)propionamide 
• 10431-98-8 2-ethyl-4,5-dihydrooxazole 
• 13670-31-0 2-(4,5-dihydro-oxazol-2-yl)-propan-1-ol 

Downstream Products

• 1221448-13-0 C₁₂H₁₅NOS 

Relevant articles and documents

Asymmetric hetero-Diels-Alder reactions of alkenyldihydrooxazoles. Synthesis of oxazolo[3,2-c]pyrimidines and related compounds

Alkenyldihydrooxazoles undergo a highly diastereoselective formal aza-Diels-Alder reaction with aryl and arenesulfonyl isocyanates to give oxazolo[3,2-c]pyrimidines. Depending on the substitution pattern of the alkenyldihydrooxazole, these compounds may then undergo addition of a second equivalent of the isocyanate to give either tetrahydrooxazoIo[3,2-c]pyrimidine-8-carboxamides or octahydroazeto[2,3-7]oxazolo[3,2c]pyrimidines. The second addition is sensitive to steric and electronic factors, and can be prevented in some cases. The Royal Society of Chemistry 1999.