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D115207

Sigma-Aldrich

6-Methyluracil

97%

Sinónimos:

2,4-Dihydroxy-6-methylpyrimidine

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About This Item

Fórmula empírica (notación de Hill):
C5H6N2O2
Número de CAS:
626-48-2
Peso molecular:
126.11
Beilstein/REAXYS Number:
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

signalword

Warning

hcodes

H361

pcodes

P281

Hazard Classifications

Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Ácido acrílico anhydrous, contains 200 ppm MEHQ as inhibitor, 99%

Sigma-Aldrich

147230

Ácido acrílico

Polybrene Infection / Transfection Reagent A highly efficient method of gene transfer into mammalian cells leveraging infection with retroviral vectors.

Sigma-Aldrich

TR-1003

Polybrene Infection / Transfection Reagent

Lucie Brulíková et al.
Carbohydrate research, 346(14), 2136-2144 (2011-08-26)
A number of 5-alkoxymethyluracil analogues were synthesized to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their corresponding nucleosides 2. All prepared compounds were submitted to cytotoxic activity
M Iu Gerasimenko et al.
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.
Fabio C Tucci et al.
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
Xiao Lu et al.
Bioorganic & medicinal chemistry, 15(23), 7399-7407 (2007-09-18)
Novel compounds 1a-u, which can be considered as hybrid analogues of MKC-442 and pyridinon, have been synthesized and evaluated as inhibitors of HIV-1 reverse transcriptase (HIV-1 RT). Starting from 6-methyluracil 2, 1-alkylated-5-bromomethyl-6-methyluracils 8 was prepared in four steps by hydroxymethylation
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.
Elzbieta Wyrzykiewicz et al.
Rapid communications in mass spectrometry : RCM, 19(4), 580-584 (2005-01-29)
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