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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 of 2,6-DI-TERT-BUTYLPYRIDINE

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

PubMed

TitleDatePubMed
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 Mar 14
Development of an ion mobility spectrometer for use in an atmospheric pressure ionization ion mobility spectrometer/mass spectrometer instrument for fast screening analysis.
2004
Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions.
2004 Jan 23
Simple synthesis of a weak nucleophilic base (4-ethyl-2,6-diisopropyl-3,5-dimethylpyridine) evidencing a double Janus group effect.
2004 Jan 23
Tetraalkylammonium halides as chemical standards for positive electrospray ionization with ion mobility spectrometry/mass spectrometry.
2005
Probing surface basicity of solid acids with an aminobenzodifurandione dye as the solvatochromic probe.
2005 Apr 21
Intrinsic acidity of dimethylhalonium ions: evidence for hyperconjugation in dimethylhalonium ylides in the gas phase.
2006 Mar 31
Interfacing an aspiration ion mobility spectrometer to a triple quadrupole mass spectrometer.
2007 Apr
Adjusting mobility scales of ion mobility spectrometers using 2,6-DtBP as a reference compound.
2008 Sep 15
Consequences of acid strength for isomerization and elimination catalysis on solid acids.
2009 May 13
MSU-S mesoporous materials: an efficient catalyst for isomerization of alpha-pinene.
2010 Oct
Separation of different ion structures in atmospheric pressure photoionization-ion mobility spectrometry-mass spectrometry (APPI-IMS-MS).
2010 Sep
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:05:33 GMT 2023
Edited
by admin
on Sat Dec 16 02:05:33 GMT 2023
Record UNII
OI9LF0H4MM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DI-TERT-BUTYLPYRIDINE
MI  
Systematic Name English
2,6-BIS(1,1-DIMETHYLETHYL)PYRIDINE
Systematic Name English
2,6-DI-TERT-BUTYLPYRIDINE [MI]
Common Name English
NSC-175805
Code English
PYRIDINE, 2,6-BIS(1,1-DIMETHYLETHYL)-
Systematic Name English
Code System Code Type Description
NSC
175805
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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CAS
585-48-8
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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FDA UNII
OI9LF0H4MM
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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WIKIPEDIA
2,6-DI-TERT-BUTYLPYRIDINE
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID80207217
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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PUBCHEM
68510
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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MERCK INDEX
m4315
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
209-557-6
Created by admin on Sat Dec 16 02:05:33 GMT 2023 , Edited by admin on Sat Dec 16 02:05:33 GMT 2023
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