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D115207

Sigma-Aldrich

6-Methyluracil

97%

Synonym(s):

2,4-Dihydroxy-6-methylpyrimidine

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About This Item

Empirical Formula (Hill Notation):
C5H6N2O2
CAS Number:
626-48-2
Molecular Weight:
126.11
Beilstein:
115647
EC Number:
210-949-4
MDL number:
MFCD00006028
UNSPSC Code:
12352100
PubChem Substance ID:
24893364
NACRES:
NA.22

Assay

97%

form

powder

mp

318 °C (dec.) (lit.)

SMILES string

CC1=CC(=O)NC(=O)N1

InChI

1S/C5H6N2O2/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)

InChI key

SHVCSCWHWMSGTE-UHFFFAOYSA-N

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Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H361

Precautionary Statements

P281

Hazard Classifications

Repr. 2

Storage Class Code

11 - 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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP1539
MKCN3526
MKCG3746
MKCF7942
MKCF0324

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Electron impact mass spectral study of 1,2-di-o-(m- and p-)nitro-(bromo-)benzyl-2-thio-6-methyluracils and 1,2-di-o-(m- and p-)nitro-(bromo-)benzyl-2-thio-5-bromo-6-methyluracils.
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[Surgical infected wound treatment in patients with severe gastrointestinal ulcer hemorrhage].
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E B Romanenko et al.
Eksperimental'naia i klinicheskaia farmakologiia, 70(4), 7-10 (2007-12-15)
Comparative study of the effects of methyluracil and betamecil showed that a fourfold oral administration of betamecil in a dose of 10 mg/kg leads to a considerable increase in the orientation-and-search reaction in the open field test. This drug effect
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Voprosy kurortologii, fizioterapii, i lechebnoi fizicheskoi kultury, (2)(2), 27-31 (2006-06-07)
Clinical, biochemical, experimental, heat physical studies and mathematical calculations have shown that combined effect of drug-laser can be differentiated into the following effects: photophoresis, light pressure and photodynamic effect.
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Chirality, 17(9), 559-564 (2005-10-01)
1-(2,6-Difluorobenzyl)-3-[(2R)-amino-2-phenethyl]-5-(2-fluoro-3-methoxyphenyl)-6-methyluracil (6), a potent and orally active antagonist of the human gonadotropin-releasing hormone receptor, exists as a pair of atropisomers in solution, which was detected by NMR spectroscopy, and separable by HPLC. In addition to a (R)-configured benzylamine, there is
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