Propane,2-(ethenyloxy)-2-methyl-
Product Information
Molecular Formula
C6H12O
Molecular Weight
100.16
Description
Propane,2-(ethenyloxy)-2-methyl- is a pivotal biomedical compound. Its indispensability stems from its critical involvement in the manufacture of diverse pharmaceuticals and remedies, aimed at combating an array of maladies. This compound's utility extends to the formulation of therapeutic agents, which effectively target distinct ailments, bolstering their remedial effects and potential for ultimate eradication.
Synonyms
TERT-BUTYL VINYL ETHER; T-BUTYL VINYL ETHER; VINYL TERTIARY-BUTYL ETHER; VINYL T-BUTYL ETHER; 2-(ethenyloxy)-2-methyl-propan; 2-(Ethenyloxy)-2-methylpropane; 2-Methyl-2-vinyloxy-propane; Ether,tert-butylvinyl
IUPAC Name
2-ethenoxy-2-methylpropane
SMILES
CC(C)(C)OC=C
InChI
InChI=1S/C6H12O/c1-5-7-6(2,3)4/h5H,1H2,2-4H3
InChI Key
PGYJSURPYAAOMM-UHFFFAOYSA-N
Boiling Point
75.0±0.0 °C at 760 mmHg
Melting Point
75-76°C(lit.)
Flash Point
1.4 °CF - closed cup
Purity
98%
Density
0.8±0.1 g/cm3
Appearance
Liquid
Storage
Refrigerator (+4°C) + Flammables area
Refractive Index
n20/D 1.398 (lit.)
Safety Information
Hazards
H225 - H315
Precautionary Statement
P210 - P302 + P352
Signal Word
Danger
Computed Properties
XLogP3
1.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
100.088815002 g/mol
Monoisotopic Mass
100.088815002 g/mol
Topological Polar Surface Area
9.2Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
59.1
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-114085631-A | Adhesive composition, method for producing the same, and article using the same | 2021-12-02 |
| CN-113926491-A | Self-adhesive composite nanogel suitable for anhydrous environment and preparation method thereof | 2021-11-17 |
| CN-113941301-A | Solvent-free preparation method of polymer microspheres | 2021-10-25 |
| CN-113979843-A | Method for preparing alkenyl ether by direct catalytic cracking | 2021-09-23 |
| CN-113788975-A | Surface treatment method of LCP material | 2021-09-14 |
| JP-2022013755-A | Tile construction method and adhesive composition | 2021-06-17 |
| KR-102322586-B1 | Waterproof coating agent manufacturing method and construction method using thereof | 2021-06-01 |
| CN-112500570-A | Flexible display device, polyamic acid varnish for display, and polyimide film | 2021-02-04 |
| CN-112500570-B | Flexible display device, polyamic acid varnish for display, and polyimide film | 2021-02-04 |
| JP-2021073352-A | Curable composition and its cured product | 2021-01-29 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22897604 | 2012-09-06 | Kinetic study of gas-phase reactions of OH and NO3 radicals and O3 with iso-butyl and tert-butyl vinyl ethers | The journal of physical chemistry. A |
| 22534197 | 2012-08-01 | Mechanistic and kinetic study on the ozonolysis of n-butyl vinyl ether, i-butyl vinyl ether and t-butyl vinyl ether | Chemosphere |
| 22096568 | 2011-01-01 | Construction and characterization of single-chain variable fragment antibody library derived from germline rearranged immunoglobulin variable genes | PloS one |
| 18605755 | 2008-08-01 | Photochemical cycloaddition of mono-, 1,1-, and 1,2-disubstituted olefins to a chiral 2(5H)-furanone. Diastereoselective synthesis of (+)-lineatin | The Journal of organic chemistry |
| 16834058 | 2005-08-11 | Quantum theory of atoms in molecules analysis on the conformational preferences of vinyl alcohol and related ethers | The journal of physical chemistry. A |
| 11681946 | 2001-11-02 | Hetero-Diels-Alder reactions of alpha-aryl-beta-monohalo-alpha-nitrosoethylenes: diastereoselective synthesis of 6-substituted 3-aryl-4-halo-5,6-dihydro-4H-1,2-oxazines | The Journal of organic chemistry |
