Home Other Building Blocks 2,6-Di-tert-butylpyridine

2,6-Di-tert-butylpyridine

CAS No.:
585-48-8
Catalog Number:
AG003323
Molecular Formula:
C13H21N
Molecular Weight:
191.3125
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$13
- +
5g
95%
In Stock USA
United States
$30
- +
10g
95%
In Stock USA
United States
$49
- +
25g
95%
In Stock USA
United States
$95
- +
100g
95%
In Stock USA
United States
$275
- +
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
Properties