585-48-8 | 2,6-Di-tert-butylpyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$11.00	$8.00
5g	98%	in stock	$14.00	$10.00
10g	98%	in stock	$17.00	$12.00
25g	98%	in stock	$42.00	$30.00
100g	98%	in stock	$167.00	$117.00

Description

• Catalog Number: AB43731
• Chemical Name: 2,6-Di-tert-butylpyridine
• CAS Number: 585-48-8
• Molecular Formula: C13H21N
• Molecular Weight: 191.3125
• MDL Number: MFCD00006306
• SMILES: CC(c1cccc(n1)C(C)(C)C)(C)C
• NSC Number: 175805

Computed Properties

• Complexity: 162
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 4.1

Literature

• 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