2,6-DI-TERT-BUTYLPYRIDINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C13H21N
Molecular Weight	191.3125
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(C)(C)C1=CC=CC(=N1)C(C)(C)C

InChI

InChIKey=UWKQJZCTQGMHKD-UHFFFAOYSA-N

InChI=1S/C13H21N/c1-12(2,3)10-8-7-9-11(14-10)13(4,5)6/h7-9H,1-6H3

HIDE SMILES / InChI

Molecular Formula	C13H21N
Molecular Weight	191.3125
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
MSU-S mesoporous materials: an efficient catalyst for isomerization of alpha-pinene.	2010-10	20483595
Separation of different ion structures in atmospheric pressure photoionization-ion mobility spectrometry-mass spectrometry (APPI-IMS-MS).	2010-09	20605730
Consequences of acid strength for isomerization and elimination catalysis on solid acids.	2009-05-13	19374417
Adjusting mobility scales of ion mobility spectrometers using 2,6-DtBP as a reference compound.	2008-09-15	18761181
Interfacing an aspiration ion mobility spectrometer to a triple quadrupole mass spectrometer.	2007-04	17477679
Intrinsic acidity of dimethylhalonium ions: evidence for hyperconjugation in dimethylhalonium ylides in the gas phase.	2006-03-31	16555813
Probing surface basicity of solid acids with an aminobenzodifurandione dye as the solvatochromic probe.	2005-04-21	16851833
Tetraalkylammonium halides as chemical standards for positive electrospray ionization with ion mobility spectrometry/mass spectrometry.	2005	16200656
Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions.	2004-01-23	14735517
Simple synthesis of a weak nucleophilic base (4-ethyl-2,6-diisopropyl-3,5-dimethylpyridine) evidencing a double Janus group effect.	2004-01-23	14725470
Development of an ion mobility spectrometer for use in an atmospheric pressure ionization ion mobility spectrometer/mass spectrometer instrument for fast screening analysis.	2004	15565719
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.	2001-03-14	11456856

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:07:57 GMT 2025` Edited by `admin` on `Mon Mar 31 21:07:57 GMT 2025`
Record UNII	OI9LF0H4MM
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-175805

Preferred Name

English

2,6-DI-TERT-BUTYLPYRIDINE

Systematic Name

English

2,6-BIS(1,1-DIMETHYLETHYL)PYRIDINE

Systematic Name

English

2,6-DI-TERT-BUTYLPYRIDINE [MI]

Common Name

English

PYRIDINE, 2,6-BIS(1,1-DIMETHYLETHYL)-

Systematic Name

English

Code System Code Type Description

NSC

175805