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
Canonical 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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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