D115207
6-Methyluracil
97%
Synonym(s):
2,4-Dihydroxy-6-methylpyrimidine
Sign Into View Organizational & Contract Pricing
Select a Size
100 G
$48.83
$48.83
List Price$51.40Save 5%Web-Only Promotion
Available to ship onApril 15, 2025Details
Request a Bulk Order
All Photos(2)
Select a Size
Change View
100 G
$48.83
About This Item
Empirical Formula (Hill Notation):
C5H6N2O2
CAS Number:
Molecular Weight:
126.11
Beilstein/REAXYS Number:
115647
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$48.83
List Price$51.40Save 5%Web-Only Promotion
Available to ship onApril 15, 2025Details
Request a Bulk Order
Recommended Products
![2-{[1-(tert-Butoxycarbonyl)-4-piperidinyl]sulfonyl}benzoic acid AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/224/106/eee847a5-ad90-45e6-b100-f59ed97f8957/640/eee847a5-ad90-45e6-b100-f59ed97f8957.png)
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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.
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
[Surgical infected wound treatment in patients with severe gastrointestinal ulcer hemorrhage].
V V Ganzhiĭ
Klinichna khirurhiia, (11-12)(11-12), 18-19 (2003-01-29)
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
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
