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585-48-8 | 2,6-Di-tert-butylpyridine
CAS No: 585-48-8 Catalog No: AG003323 MDL No:MFCD00006306
Product Description
Catalog Number:
AG003323
Chemical Name:
2,6-Di-tert-butylpyridine
CAS Number:
585-48-8
Molecular Formula:
C13H21N
Molecular Weight:
191.3125
MDL Number:
MFCD00006306
IUPAC Name:
2,6-ditert-butylpyridine
InChI:
InChI=1S/C13H21N/c1-12(2,3)10-8-7-9-11(14-10)13(4,5)6/h7-9H,1-6H3
InChI Key:
UWKQJZCTQGMHKD-UHFFFAOYSA-N
SMILES:
CC(c1cccc(n1)C(C)(C)C)(C)C
EC Number:
209-557-6
UNII:
OI9LF0H4MM
NSC Number:
175805
Properties
Complexity:
162
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
191.167g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
191.318g/mol
Monoisotopic Mass:
191.167g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
12.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.1
Literature
| Title | Journal |
|---|---|
| Silylium ion-catalyzed challenging Diels-Alder reactions: the danger of hidden proton catalysis with strong Lewis acids. | Journal of the American Chemical Society 20120307 |
| Letter: A simple ion source set-up for desorption/ionization on silicon with ion mobility spectrometry and ion mobility spectrometry-mass spectrometry. | European journal of mass spectrometry (Chichester, England) 20110101 |
| MSU-S mesoporous materials: an efficient catalyst for isomerization of alpha-pinene. | Bioresource technology 20101001 |
| Separation of different ion structures in atmospheric pressure photoionization-ion mobility spectrometry-mass spectrometry (APPI-IMS-MS). | Journal of the American Society for Mass Spectrometry 20100901 |
| Consequences of acid strength for isomerization and elimination catalysis on solid acids. | Journal of the American Chemical Society 20090513 |
| Adjusting mobility scales of ion mobility spectrometers using 2,6-DtBP as a reference compound. | Talanta 20080915 |
| Interfacing an aspiration ion mobility spectrometer to a triple quadrupole mass spectrometer. | The Review of scientific instruments 20070401 |
| Intrinsic acidity of dimethylhalonium ions: evidence for hyperconjugation in dimethylhalonium ylides in the gas phase. | The Journal of organic chemistry 20060331 |
| Probing surface basicity of solid acids with an aminobenzodifurandione dye as the solvatochromic probe. | The journal of physical chemistry. B 20050421 |
| Tetraalkylammonium halides as chemical standards for positive electrospray ionization with ion mobility spectrometry/mass spectrometry. | Rapid communications in mass spectrometry : RCM 20050101 |
| Simple synthesis of a weak nucleophilic base (4-ethyl-2,6-diisopropyl-3,5-dimethylpyridine) evidencing a double Janus group effect. | The Journal of organic chemistry 20040123 |
| Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions. | Chemistry (Weinheim an der Bergstrasse, Germany) 20040123 |
| Development of an ion mobility spectrometer for use in an atmospheric pressure ionization ion mobility spectrometer/mass spectrometer instrument for fast screening analysis. | Rapid communications in mass spectrometry : RCM 20040101 |
| Tuning the strain and polymerizability of organometallic rings: the synthesis, structure, and ring-opening polymerization behavior of [2]ferrocenophanes with C-SI, C-P, and C-S bridges. | Journal of the American Chemical Society 20010314 |
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