跳转至内容
Merck
CN

349801

Sigma-Aldrich

1,3-二甲基脲嘧啶

99%

别名:

1,3-二甲基-2,4(1H,3H)-嘧啶二酮, 1,3-二甲基-2,4-嘧啶二酮

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C6H8N2O2
化学文摘社编号:
分子量:
140.14
Beilstein:
124074
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

方案

99%

表单

powder

mp

119-122 °C (lit.)

SMILES字符串

CN1C=CC(=O)N(C)C1=O

InChI

1S/C6H8N2O2/c1-7-4-3-5(9)8(2)6(7)10/h3-4H,1-2H3

InChI key

JSDBKAHWADVXFU-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

1,3-Dimethyluracil is a pyrimidine derivative. Stability of the C6-centered carbanions derived from 1,3-dimethyluracil has been investigated in the gas phase and in DMSO and water solutions. The excited state structural dynamics of 1,3-dimethyluracil (DMU) in water and acetonitrile has been studied by resonance Raman spectroscopy. Crystal structure of 1,3-dimethyluracil has been reported. Ultraviolet irradiation of aqueous 1,3-dimethyluracil results in hydration of the 5:6 double bond of the uracil ring to form 1,3-dimethyl-6-oxy-hydrouracil.

应用

1,3-Dimethyluracil is suitable reagent used to investigate the steady-state absorption and fluorescence spectra of uracil derivatives. It may be used in the preparation of 2,6-dihydroxynicotinamide.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

J De Taeye et al.
Journal of pharmaceutical sciences, 74(6), 660-663 (1985-06-01)
The interaction between caffeine and hydroxylic derivatives (phenols, water) has been studied by infrared (IR) spectroscopy in 1,2-dichloroethane. The formation constants, enthalpies, and entropies of complex formation have been determined. The IR spectra in the vOH and vc=o ranges indicate
S Das et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 46(1), 7-9 (1984-07-01)
The electron adducts of uracil, 1,3-dimethyluracil and 1,3-dimethylthymine, known to protonate rapidly in aqueous solution at oxygen, are now shown to undergo a slower protonation at C(6) producing a radical centred at C(5), a reaction which can be catalysed by
Singlet excited state dynamics of uracil and thymine derivatives: A femtosecond fluorescence upconversion study in acetonitrile.
Gustavsson T, et al.
Chemical Physics Letters, 429(4), 551-557 (2006)
1, 3-Dimethyluracil: a crystal structure without hydrogen bonds.
Banerjee A, et al.
Acta Crystallographica Section B, Structural Science, 33(1), 90-94 (1977)
Amir Golan et al.
Journal of visualized experiments : JoVE, (68)(68), doi:10-doi:10 (2012-11-15)
Tunable soft ionization coupled to mass spectroscopy is a powerful method to investigate isolated molecules, complexes and clusters and their spectroscopy and dynamics(1-4). Fundamental studies of photoionization processes of biomolecules provide information about the electronic structure of these systems. Furthermore

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持