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Details

Stereochemistry ACHIRAL
Molecular Formula C6H9N3
Molecular Weight 123.1558
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINO-4,6-DIMETHYLPYRIMIDINE

SMILES

CC1=CC(C)=NC(N)=N1

InChI

InChIKey=IDQNBVFPZMCDDN-UHFFFAOYSA-N
InChI=1S/C6H9N3/c1-4-3-5(2)9-6(7)8-4/h3H,1-2H3,(H2,7,8,9)

HIDE SMILES / InChI

Molecular Formula C6H9N3
Molecular Weight 123.1558
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
2-Amino-4,6-dimethyl-pyrimidin-1-ium 1-oxo-2,6,7-trioxa-1λ-phosphabicyclo-[2.2.2]octane-4-carboxyl-ate.
2010-06-05
2-Amino-4,6-dimethyl-pyrimidine-anthranilic acid (1/1).
2010-02-03
N-(6-Methyl-2-pyrid-yl)formamide.
2009-12-16
2-Amino-4,6-dimethyl-pyrimidinium chloro-acetate.
2009-10-31
2-Amino-4,6-dimethyl-pyrimidinium dihydrogenphosphate.
2009-10-03
Two novel silver(I) coordination polymers: poly[(mu2-2-aminopyrimidine-kappa2N1:N3)bis(mu3-thiocyanato-kappa3S:S:S)disilver(I)] and poly[(2-amino-4,6-dimethylpyrimidine-kappaN)(mu3-thiocyanato-kappa3N:S:S)silver(I)].
2009-10
(2-Amino-4,6-dimethyl-pyrimidine-κN)(2-amino-4-methyl-pyrimidine-κN)silver(I) nitrate.
2009-09-05
(2-Amino-4,6-dimethyl-pyrimidine-κN)(2-amino-4-methyl-pyrimidine-κN)silver(I) perchlorate.
2009-09-05
2-Amino-4,6-dimethyl-pyrimidine-benzoic acid (1/1).
2009-06-17
2-Amino-4,6-dimethyl-pyrimidinium 3,5-dinitro-benzoate dihydrate.
2008-01-11
Hydrogen-bonding patterns in the cocrystal 2-amino-4,6-dimethoxy-pyrimidine-anthranilic acid (1/1).
2007-12-06
R2(2)(8) motifs in Aminopyrimidine sulfonate/carboxylate interactions: crystal structures of pyrimethaminium benzenesulfonate monohydrate (2:2:1) and 2-amino-4,6-dimethylpyrimidinium sulfosalicylate dihydrate (4:2:2).
2007-11-13
Stepwise charge transfer complexation of some pyrimidines with sigma-acceptor iodine involving a new unconventional acceptor.
2007-11
Hydrolytic degradation of azimsulfuron, a sulfonylurea herbicide.
2007-07
Hydrogen-bonding and pi-pi interactions in 2-amino-4,6-dimethylpyrimidinium salicylate.
2006-10
Degradation of anilinopyrimidine fungicides photoinduced by iron(III)-polycarboxylate complexes.
2006-09
A structural and magnetic study of organolanthanide(III) amides.
2006-04-07
Hydrogen-bonding patterns in trimethoprim picolinate and 2-amino-4,6-dimethylpyrimidinium picolinate hemihydrate.
2006-02
Photoinduced amino-imino tautomerization reaction in 2-aminopyrimidine and its methyl derivatives with acetic acid.
2005-12
Hydrogen-bonding patterns in 2-amino-4,6-dimethylpyrimidinium hydrogen sulfate.
2005-02
In vitro and in vivo antileishmanial activity of 2-amino-4,6-dimethylpyridine derivatives against Leishmania mexicana.
2002-12
Spectral and photophysical studies of inclusion complexes of 2-amino-4,6-dimethyl pyrimidine with beta-cyclodextrin.
2002-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:38:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:38:30 GMT 2025
Record UNII
4S48MI253M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINO-4,6-DIMETHYLPYRIMIDINE
Systematic Name English
NSC-3278
Preferred Name English
4,6-DIMETHYLPYRIMIDINE-2-AMINE
Systematic Name English
AMINO-4,6-DIMETHYLPYRIMIDINE, 2-
Systematic Name English
2-AMINO-4,6-DIMETHYL-PYRIMIDINE
Systematic Name English
(4,6-DIMETHYLPYRIMIDIN-2-YL)AMINE
Systematic Name English
2-PYRIMIDINAMINE, 4,6-DIMETHYL-
Systematic Name English
4,6-DIMETHYL-2-PYRIMIDINAMINE
Systematic Name English
4,6-DIMETHYL-2-AMINOPYRIMIDINE
Systematic Name English
PYRIMIDINE, 2-AMINO-4,6-DIMETHYL-
Systematic Name English
Code System Code Type Description
PUBCHEM
13021
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY
FDA UNII
4S48MI253M
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-181-5
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY
NSC
3278
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY
CAS
767-15-7
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID8052510
Created by admin on Mon Mar 31 19:38:30 GMT 2025 , Edited by admin on Mon Mar 31 19:38:30 GMT 2025
PRIMARY