2-Isopropyl-2-oxazoline
Product Information
Molecular Formula
C6H11NO
Molecular Weight
113.16
Description
2-Isopropyl-2-oxazoline is a biomedical compound that finds extensive application within the biomedical industry where it engenders drugs and remedies. Its undeniable potency lies in tackling a plethora of ailments encompassing cancer, inflammation, and cardiovascular maladies. Possessing idiosyncratic chemical attributes, this compound heralds a propitious realm of therapeutic potentialities within the expansive realm of biomedicine.
Synonyms
2-propan-2-yl-4,5-dihydro-1,3-oxazole; 2-(propan-2-yl)-4,5-dihydro-1,3-oxazole; 2-Isopropyl-1,3-oxazol-2-ine; SCHEMBL152241; 2-Isopropyl-4,5-dihydrooxazole; 2-Isopropyl-4,5-dihydro-oxazole; 2-Isopropyl-2-oxazoline, >=96.5% (GC)
IUPAC Name
2-propan-2-yl-4,5-dihydro-1,3-oxazole
SMILES
CC(C)C1=NCCO1
InChI
InChI=1S/C6H11NO/c1-5(2)6-7-3-4-8-6/h5H,3-4H2,1-2H3
InChI Key
FVEZUCIZWRDMSJ-UHFFFAOYSA-N
Boiling Point
138°C
Flash Point
73.4 °CF
Purity
95%
Density
0.95
Storage
2-8°C
Refractive Index
1.4330 to 1.4380
Safety Information
Hazards
H226
Precautionary Statement
P210 - P370 + P378
Computed Properties
XLogP3
0.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
113.084063974 g/mol
Monoisotopic Mass
113.084063974 g/mol
Topological Polar Surface Area
21.6Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
107
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113004517-A | Modified epoxy resin, adhesive, preparation method and application thereof | 2021-03-08 |
| AU-2021100766-A4 | A Preparation Method of (S)-(+)-2, 2-dimethyl cyclopropanecarboxamide | 2021-02-08 |
| CN-112851479-A | Method for preparing chiral alkyl compound by catalyzing asymmetric hydrogenation reaction of olefin with iron complex catalyst | 2021-01-22 |
| CN-112759721-A | Thermo-sensitive polylactic acid high polymer material and preparation method and application thereof | 2021-01-20 |
| KR-20200129076-A | Adhesive composition and adhesive film comprising the cured product thereof | 2020-11-06 |
| US-2022080267-A1 | Golf ball | 2020-09-11 |
| US-2022062858-A1 | Super-adsorbing porous thermo-responsive desiccants | 2020-09-03 |
| WO-2022040649-A1 | Diffusivity contrast agents for medical imaging | 2020-08-21 |
| JP-2022031008-A | Original plate for forming ink film | 2020-08-07 |
| WO-2022018651-A2 | Synthesis of heterocyclic compounds from carboxamide and carboxamide derivatives with haloalkanols | 2020-07-21 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 23031697 | 2012-10-01 | Water uptake of poly(2-N-alkyl-2-oxazoline)s: temperature-dependent Fourier transform infrared (FT-IR) spectroscopy and two-dimensional correlation analysis (2DCOS) | Applied spectroscopy |
| 22324756 | 2012-03-01 | Facile approach to grafting of poly(2-oxazoline) brushes on macroscopic surfaces and applications thereof | ACS applied materials & interfaces |
| 21993910 | 2011-11-01 | Self-assembly of poly(2-alkyl-2-oxazoline)s by crystallization in ethanol-water mixtures below the upper critical solution temperature | Macromolecular rapid communications |
| 21669437 | 2011-09-15 | Effect of structural isomerism and polymer end group on the pH-stability of hydrogen-bonded multilayers | Journal of colloid and interface science |
| 16391777 | 2006-01-21 | Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis | Organic & biomolecular chemistry |
| 15762680 | 2005-03-01 | Bottom-up synthesis of hyaluronan and its derivatives via enzymatic polymerization: direct incorporation of an amido functional group | Biomacromolecules |
