2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide
Product Information
Molecular Formula
C14H22NO
Molecular Weight
220.33
Description
Block Copolymer Synthesis Using a Commercially Available NMP Inititator
Synonyms
1,1-Dimethylethyl-2-methyl-1-phenylpropyl nitroxide, tert-Butyl 1-phenyl-2-methylpropyl nitroxide, NMP universal alkoxyamine nitroxide
SMILES
CC(C)C(C1=CC=CC=C1)N(C(C)(C)C)[O]
InChI
InChI=1S/C14H22NO/c1-11(2)13(15(16)14(3,4)5)12-9-7-6-8-10-12/h6-11,13H,1-5H3
InChI Key
VGHCMXLEZFMZOZ-UHFFFAOYSA-N
Flash Point
204.8 °F
Purity
98%
Appearance
solid
Storage
−20°C
Refractive Index
n20/D 1.515
Computed Properties
XLogP3
3.6
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
4
Exact Mass
220.170139325 g/mol
Monoisotopic Mass
220.170139325 g/mol
Topological Polar Surface Area
4.2Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
201
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
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 |
|---|---|---|
| US-2009081452-A1 | Transparent adhesive tape | 2007-09-20 |
| US-2009042808-A1 | Use of mitochondria-targeted electron scavengers as anti-inflammatory agents | 2007-08-08 |
| US-2009208739-A1 | Adhesive film with high optical transperancy, as an anti-splinter cover for adhering to glass windows in electronic components for consumer items | 2006-07-28 |
| US-2009186285-A1 | Color filter composition | 2006-07-11 |
| US-2008295404-A1 | Odorant Mixture for Odorless Gas Fuel | 2005-10-11 |
| US-2009088518-A1 | Polymers obtained via nitroxyl radical polymerization | 2005-08-30 |
| US-7858694-B2 | Polymers obtained via nitroxyl radical polymerization | 2005-08-30 |
| US-2009221739-A1 | Process for the Post-Modification of Homo and Copolymers Prepared by Controlled Free Radical Polymerization Processes | 2005-01-11 |
| US-2011224375-A1 | Process for the post-modification of homo and copolymers prepared by controlled free radical polymerization processes | 2005-01-11 |
| US-2007225397-A1 | In-Can Stabilizers | 2004-09-03 |
