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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2
Molecular Weight 94.1145
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLPYRAZINE

SMILES

CC1=NC=CN=C1

InChI

InChIKey=CAWHJQAVHZEVTJ-UHFFFAOYSA-N
InChI=1S/C5H6N2/c1-5-4-6-2-3-7-5/h2-4H,1H3

HIDE SMILES / InChI

Molecular Formula C5H6N2
Molecular Weight 94.1145
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Crystal transformation and host molecular motions in CO2 adsorption process of a metal benzoate pyrazine (M(II) = Rh, Cu).
2010-03-24
Coffee aroma--statistical analysis of compositional data.
2009-12-15
2,5-Dimethyl-pyrazine 1,4-dioxide.
2009-11-11
2-Methyl-pyrazine 1,4-dioxide.
2009-11-07
Syntheses, structures, and photoluminescence of a series of silver(I) sulfonates with pyrazine derivatives.
2009-10-14
Scaled quantum chemical calculations and FTIR, FT-Raman spectral analysis of 2-Methylpyrazine.
2009-05
A binuclear Cu(II) metallacycle capable of discerning between pyrazine and its different methyl-substituted derivatives based on reversible intracage metal-ligand binding.
2009
Structural and magnetic study of O2 molecules arranged along a channel in a flexible single-crystal host family.
2008-12-31
Conversion of methane to liquid products, hydrogen, and ammonia with environmentally friendly condition-based microgap discharge.
2008-12
Poly[μ-4,4'-bipyridine-κN:N'-μ-thio-cyanato-κN:S-copper(I)].
2008-10-18
Identification and monitoring of intermediates and products in the acrylamide pathway using online analysis.
2008-08-13
Rotationally resolved IR-diode laser studies of ground-state CO2 excited by collisions with vibrationally excited pyridine.
2008-03-27
Competition between photochemistry and energy transfer in UV-excited diazabenzenes. 4. UV photodissociation of 2,3-, 2,5-, and 2,6-dimethylpyrazine.
2007-12-27
Poly[[(μ(2)-2-amino-4,5-dimethybenzene-sulfonato-κN:O)(μ(2)-2-methyl-pyrazine-κN:N')silver(I)] monohydrate].
2007-12-06
Degradation of 2,5-dimethylpyrazine by Rhodococcus erythropolis strain DP-45 isolated from a waste gas treatment plant of a fishmeal processing company.
2007-10
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
2007-01-24
Construction of polyoxometalates-based coordination polymers through direct incorporation between polyoxometalates and the voids in a 2D network.
2006-12-25
Role of the solvent glycerol in the Maillard reaction of d-fructose and l-alanine.
2006-01-25
Tuning the electronic communication and rates of intramolecular electron transfer of dimers of trinuclear ruthenium clusters: bridging and ancillary ligand effects.
2006-01-23
Determination of the 2H/1H and 15N/14N ratios of Alkylpyrazines from coffee beans (Coffea arabica L. and Coffea canephoravar. robusta) by isotope ratio mass spectrometry.
2005-10-05
Reactivity of epicatechin in aqueous glycine and glucose maillard reaction models: quenching of C2, C3, and C4 sugar fragments.
2005-05-18
Mixed valence isomers.
2005-03-02
Testing olfactory foraging strategies in an Antarctic seabird assemblage.
2004-09
Comparative structural studies of iodide complexes of uranium(III) and lanthanide(III) with hexadentate tetrapodal neutral N-donor ligands.
2004-08-09
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.
2004-05-12
Long-range ferromagnetic ordering in two-dimensional coordination polymers Co[N(CN)2]2(L) [L = pyrazine dioxide (pzdo) and 2-methyl pyrazine dioxide (mpdo)] with dual mu- and mu3-[N(CN)2] bridges.
2003-08-25
Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery.
2003-05-16
Effects of heterocyclic aromatic substituents on binding affinities at two distinct sites of somatostatin receptors. Correlation with the electrostatic potential of the substituents.
2003-05-08
AgC(CN)3-based coordination polymers.
2003-04-21
The important effect of ligand architecture on the selectivity of metal ion recognition in An(III)/Ln(III) separation with N-donor extractants.
2002-12-07
Effects of carnosine on volatile generation from Maillard reaction of ribose and cysteine.
2002-04-10
Detection and quantification of ochratoxin A and deoxynivalenol in barley grains by GC-MS and electronic nose.
2002-02-05
Interaction-induced enhancement in the activity and selectivity of a titania-supported ammonium salt of a 12-molybdophosphoric acid catalyst during ammoxidation of 2-methylpyrazine.
2001-10-21
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.
1994-08-17
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:32:41 GMT 2025
Edited
by admin
on Mon Mar 31 18:32:41 GMT 2025
Record UNII
RVC6500U9C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-METHYLPYRAZINE
FCC   FHFI  
Systematic Name English
FEMA NO. 3309
Preferred Name English
PYRAZINE, METHYL-
Systematic Name English
2-METHYL-1,4-DIAZINE
Systematic Name English
NSC-30412
Code English
2-METHYLPYRAZINE [FCC]
Common Name English
METHYLPYRAZINE
Systematic Name English
2-METHYLPYRAZINE [FHFI]
Common Name English
NSC-49138
Code English
MONOMETHYLPYRAZINE
Systematic Name English
PYRAZINE, 2-METHYL
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 2-METHYLPYRAZINE
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
Code System Code Type Description
PUBCHEM
7976
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
NSC
49138
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
FDA UNII
RVC6500U9C
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
JECFA MONOGRAPH
848
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
NSC
30412
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
CAS
109-08-0
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-645-8
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID4047620
Created by admin on Mon Mar 31 18:32:41 GMT 2025 , Edited by admin on Mon Mar 31 18:32:41 GMT 2025
PRIMARY