2,4-DIMETHOXYPYRIMIDINE

COC1=NC(OC)=NC=C1

InChIKey=KEVRHVMWBKFGLO-UHFFFAOYSA-N

InChI=1S/C6H8N2O2/c1-9-5-3-4-7-6(8-5)10-2/h3-4H,1-2H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Short access to 6-substituted pyrimidine derivatives by the S(RN)1 mechanism. Synthesis of 6-substituted uracils through a one-pot procedure.	2010-08-06	20590101
Identification of gp96 as a novel target for treatment of autoimmune disease in mice.	2010-03-23	20352117
Quantification of atrazine, phenylurea, and sulfonylurea herbicide metabolites in urine by high-performance liquid chromatography-tandem mass spectrometry.	2007-05	17555640
The cyclization transformation of the sulfonylurea herbicide flupyrsulfuron in the soil of winter wheat crops.	2003-08	12916776
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.	1994-08-17	8080452

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:22:55 GMT 2025` Edited by `admin` on `Mon Mar 31 19:22:55 GMT 2025`
Record UNII	980K6DH82B
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

2,4-DI-O-METHYLURACIL

Preferred Name

English

2,4-DIMETHOXYPYRIMIDINE

Systematic Name

English

PYRIMIDINE, 2,4-DIMETHOXY-

Systematic Name

English

Code System Code Type Description

CAS

3551-55-1

Created by admin on Mon Mar 31 19:22:55 GMT 2025 , Edited by admin on Mon Mar 31 19:22:55 GMT 2025

PRIMARY

PUBCHEM

137976

Created by admin on Mon Mar 31 19:22:55 GMT 2025 , Edited by admin on Mon Mar 31 19:22:55 GMT 2025

PRIMARY

EPA CompTox

DTXSID10189017

Created by admin on Mon Mar 31 19:22:55 GMT 2025 , Edited by admin on Mon Mar 31 19:22:55 GMT 2025

PRIMARY

FDA UNII

980K6DH82B

Created by admin on Mon Mar 31 19:22:55 GMT 2025 , Edited by admin on Mon Mar 31 19:22:55 GMT 2025

PRIMARY