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Details

Stereochemistry ACHIRAL
Molecular Formula C6H9N3O2
Molecular Weight 155.1546
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

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

SMILES

COC1=CC(OC)=NC(N)=N1

InChI

InChIKey=LVFRCHIUUKWBLR-UHFFFAOYSA-N
InChI=1S/C6H9N3O2/c1-10-4-3-5(11-2)9-6(7)8-4/h3H,1-2H3,(H2,7,8,9)

HIDE SMILES / InChI

Molecular Formula C6H9N3O2
Molecular Weight 155.1546
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-methyl-pyridinium 6-carb-oxy-pyridine-2-carboxyl-ate methanol monosolvate.
2010-12-08
4,6-Dimeth-oxy-pyrimidin-2-amine-2-(1H-indol-3-yl)acetic acid (1/1).
2010-09-25
Hydrogen-bonded supramolecular motifs in 2-amino-4,6-dimethoxypyrimidinium picrate and pyrimethaminium picrate dimethyl sulfoxide solvate.
2009-02
Hydrogen-bonding patterns in the cocrystal 2-amino-4,6-dimethoxy-pyrimidine-anthranilic acid (1/1).
2007-12-06
The hydrogen bonding and amino-imino tautomerization of the alkoxy-aminopyridines and amino-methoxypyrimidines with acetic acid The effects of the methoxy group.
2007-11
Structural elucidation of phototransformation products of azimsulfuron in water.
2007-08-08
Hydrolytic degradation of azimsulfuron, a sulfonylurea herbicide.
2007-07
Hydrogen-bonded supramolecular motifs in 2-amino-4,6-dimethoxypyrimidinium 4-hydroxybenzoate monohydrate, 2-amino-4,6-dimethoxypyrimidinium 6-carboxypyridine-2-carboxylate monohydrate and 2-amino-4,6-dimethoxypyrimidinium hydrogen (2R,3R)-tartrate 2-amino-4,6-dimethoxypyrimidine.
2007-05
Vibrational spectroscopy investigation using ab initio and density functional theory analysis on the structure of 2-amino-4,6-dimethoxypyrimidine.
2006-12
Sorption and degradation of azimsulfuron on iron(III)-rich soil colloids.
2004-12-29
Aerobic soil metabolism of a new herbicide, LGC-42153.
2003-01-29
Degradation of sulfosulfuron, a sulfonylurea herbicide, as influenced by abiotic factors.
2002-07-31
Hydrogen bonding in 2-amino-4,6-dimethoxypyrimidine, 2-benzylamino-4,6-bis(benzyloxy)pyrimidine and 2-amino-4,6-bis(N-pyrrolidino)pyrimidine: chains of fused rings and a centrosymmetric dimer.
2002-05
Degradation of imazosulfuron in soil.
2001-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:35:24 GMT 2025
Edited
by admin
on Mon Mar 31 19:35:24 GMT 2025
Record UNII
8B9760951K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AE-F 092944
Preferred Name English
2-AMINO-4,6-DIMETHOXYPYRIMIDINE
Systematic Name English
4,6-DIMETHOXY-2-AMINOPYRIMIDINE
Systematic Name English
J 290
Code English
AMINO-4,6-DIMETHOXYPYRIMIDINE, 2-
Systematic Name English
2-PYRIMIDINAMINE, 4,6-DIMETHOXY-
Systematic Name English
J-290
Code English
PYRIMIDINE, 2-AMINO-4,6-DIMETHOXY-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 618603
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
Code System Code Type Description
PUBCHEM
118946
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY
ECHA (EC/EINECS)
252-969-6
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY
FDA UNII
8B9760951K
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY
MESH
C518759
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY
CAS
36315-01-2
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID1074620
Created by admin on Mon Mar 31 19:35:24 GMT 2025 , Edited by admin on Mon Mar 31 19:35:24 GMT 2025
PRIMARY