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Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N
Molecular Weight 121.1796
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3,4-TRIMETHYLPYRIDINE

SMILES

CC1=CC=NC(C)=C1C

InChI

InChIKey=HOPRXXXSABQWAV-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-6-4-5-9-8(3)7(6)2/h4-5H,1-3H3

HIDE SMILES / InChI

Molecular Formula C8H11N
Molecular Weight 121.1796
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit.
2010-09-15
2,4,6-Trimethyl-pyridinium nitrate.
2010-08-21
Genome-wide mapping of quantitative trait loci for fatness, fat cell characteristics and fat metabolism in three porcine F2 crosses.
2010-07-28
Structural correlations for (1)H, (13)C and (15)N NMR coordination shifts in Au(III), Pd(II) and Pt(II) chloride complexes with lutidines and collidine.
2010-06
First principles insight into the alpha-glucan structures of starch: their synthesis, conformation, and hydration.
2010-04-14
Synthesis and biological evaluation of new imidazolium and piperazinium salts of pyropheophorbide-a for photodynamic cancer therapy.
2008-08
Nuclear magnetic resonance and ab initio studies of small complexes formed between water and pyridine derivatives in solid and liquid phases.
2007-07-12
Activity of a cationic carotenoid derivative in a mouse model of protoporphyria.
2007-05-25
Mild TiIII- and Mn/ZrIV-catalytic reductive coupling of allylic halides: efficient synthesis of symmetric terpenes.
2007-04-13
Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis.
2007-03
Ethyne-bridged (porphinato)zinc(II)-(porphinato)iron(III) complexes: phenomenological dependence of excited-state dynamics upon (porphinato)iron electronic structure.
2006-08-16
Alpha- and beta- aspartyl peptide ester formation via aspartimide ring opening.
2005-10
Monomeric, tetrameric, and polymeric copper di-tert-butyl phosphate complexes containing pyridine ancillary ligands.
2004-02-09
Asymmetric alkylation of N-toluenesulfonylimines with dialkylzinc reagents catalyzed by copper-chiral amidophosphine.
2003-12-12
Low-temperature NMR studies of the structure and dynamics of a novel series of acid-base complexes of HF with collidine exhibiting scalar couplings across hydrogen bonds.
2003-09-24
Total synthesis of anti-HIV agent chloropeptin I.
2003-07-30
Bis(pyridine)-based bromonium ions. Molecular structures of bis(2,4,6-collidine)bromonium perchlorate and bis(pyridine)bromonium triflate and the mechanism of the reactions of 1,2-bis(2'-pyridylethynyl)benzenebrominum triflate and bis(pyridine)bromonium triflate with acceptor olefins.
2003-05-16
Total syntheses of beta-carboline alkaloids, (R)-(-)-pyridindolol K1, (R)-(-)-pyridindolol K2, and (R)-(-)-pyridindolol.
2001-12-28
Inclusion compounds of tetrakis(4-nitrophenyl)methane: C-H...O networks, pseudopolymorphism, and structural transformations.
2001-05-16
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:00:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:00:50 GMT 2025
Record UNII
720P8M59GM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3,4-COLLIDINE
Preferred Name English
2,3,4-TRIMETHYLPYRIDINE
Systematic Name English
PYRIDINE, 2,3,4-TRIMETHYL-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID90176869
Created by admin on Mon Mar 31 19:00:50 GMT 2025 , Edited by admin on Mon Mar 31 19:00:50 GMT 2025
PRIMARY
PUBCHEM
16691
Created by admin on Mon Mar 31 19:00:50 GMT 2025 , Edited by admin on Mon Mar 31 19:00:50 GMT 2025
PRIMARY
CAS
2233-29-6
Created by admin on Mon Mar 31 19:00:50 GMT 2025 , Edited by admin on Mon Mar 31 19:00:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
218-775-0
Created by admin on Mon Mar 31 19:00:50 GMT 2025 , Edited by admin on Mon Mar 31 19:00:50 GMT 2025
PRIMARY
FDA UNII
720P8M59GM
Created by admin on Mon Mar 31 19:00:50 GMT 2025 , Edited by admin on Mon Mar 31 19:00:50 GMT 2025
PRIMARY