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Merck

M6631

Sigma-Aldrich

3-Methyluracil

别名:

3-MeU

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About This Item

经验公式(希尔记法):
C5H6N2O2
CAS号:
分子量:
126.11
MDL號碼:
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.51

化驗

≥98% (TLC)

形狀

powder

溶解度

1 M NaOH: 50 mg/mL, clear, colorless to faintly yellow

儲存溫度

−20°C

SMILES 字串

CN1C(=O)NC=CC1=O

InChI

1S/C5H6N2O2/c1-7-4(8)2-3-6-5(7)9/h2-3H,1H3,(H,6,9)

InChI 密鑰

VPLZGVOSFFCKFC-UHFFFAOYSA-N

一般說明

3-Methyluracil is a methylated uracil or a uracil derivative.

應用

3-Methyluracil (3-MeU) is used along with other methyl-pyrimidines to study relative physical chemical parameters.

象形圖

Health hazard

訊號詞

Warning

危險聲明

防範說明

危險分類

Carc. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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T V Chestnova et al.
Bulletin of experimental biology and medicine, 165(6), 777-780 (2018-10-26)
Bacterial biofilms provoke and/or promote the most chronic and recurrent infectious diseases. Previously, experimental models of purulent peritonitis and meningoencephalitis revealed positive antibiofilm effect of metallic nanoparticles and the absence of resistance against such nanoparticles in microorganisms. This study examines
Vibrational Feshbach resonances in uracil and thymine.
Burrow PD, Gallup GA, et al.
J. Chem. Phys. , 28, 124310-124310 (2006)
Mihajlo Etinski et al.
Physical chemistry chemical physics : PCCP, 12(19), 4915-4923 (2010-05-07)
In this work we investigated the lowest-lying electronic excitations for a series of methyl-substituted uracil derivatives, i.e., uracil, 1-methyluracil, 3-methyluracil, thymine, 1-methylthymine, 1,3-dimethyluracil, 3-methylthymine, 1,3-dimethylthymine, and their microhydrated complexes by means of coupled cluster singles and approximate doubles (CC2) and
Guifang Jia et al.
FEBS letters, 582(23-24), 3313-3319 (2008-09-09)
The human obesity susceptibility gene, FTO, encodes a protein that is homologous to the DNA repair AlkB protein. The AlkB family proteins utilize iron(II), alpha-ketoglutarate (alpha-KG) and dioxygen to perform oxidative repair of alkylated nucleobases in DNA and RNA. We
Anna Zhachkina et al.
Journal of the American Chemical Society, 131(51), 18376-18385 (2009-11-26)
The gas-phase substitution reactions of methyl chloride and 1,3-dimethyluracil (at the N1-CH(3)) are examined computationally and experimentally. It is found that, although hydrochloric acid and 3-methyluracil are similar in acidity, the leaving group abilities of chloride and N1-deprotonated 3-methyluracil are

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