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Key Documents

Safety Information

165360

Sigma-Aldrich

2,4-Dihydroxy-5,6-dimethylpyrimidine

97%

Synonym(s):

5,6-Dimethyluracil

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About This Item

Empirical Formula (Hill Notation):
C6H8N2O2
CAS Number:
Molecular Weight:
140.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

297-300 °C (dec.) (lit.)

SMILES string

CC1=C(C)C(=O)NC(=O)N1

InChI

1S/C6H8N2O2/c1-3-4(2)7-6(10)8-5(3)9/h1-2H3,(H2,7,8,9,10)

InChI key

PZVLJGKJIMBYNP-UHFFFAOYSA-N

Application

2,4-Dihydroxy-5,6-dimethylpyrimidine was used in the synthesis of mono and polyatomic titanium derivatives. It was used as staring reagent in the synthesis of 2-(4-fluorobenzoyl) substituted pyrimidine derivatives.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

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A family of titanium (IV) alkoxo complexes with N, O and O, O chelating ligands. Crystal structure of [Ti (O-i-Pr)2{2-(-)-menthoxo-pyridine}2].
Perez Y, et al.
Inorgorganica Chimica Acta, 360(2), 607-618 (2007)
Young Ae Yoon et al.
Bioorganic & medicinal chemistry letters, 20(19), 5735-5738 (2010-09-03)
A series of pyrimidine derivatives as acid pump antagonists (APAs) was synthesized and the inhibitory activities against H(+)/K(+) ATPase isolated from hog gastric mucosa were determined. After elaborating on substituents at C2 and C4 position of the pyrimidine scaffold, we

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