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Sigma-Aldrich

1,3-二甲基巴比妥酸

≥99.0% (T)

同義詞:

1,3-二甲基-2,4,6(1H,3H,5H)-嘧啶三酮

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About This Item

經驗公式（希爾表示法）:
C6H8N2O3
CAS號碼:
769-42-6
分子量：:
156.14
Beilstein:
139810
EC號碼:
212-211-7
MDL號碼:
MFCD00006675
分類程式碼代碼:
12352100
PubChem物質ID:
57649861
NACRES:
NA.22
暫時無法取得訂價和供貨情況

化驗

≥99.0% (T)

形狀

solid

燃燒殘留物

≤0.1%

mp

121-123 °C (lit.)
123-126 °C

溶解度

hot water: soluble 0.5 g/10 mL, clear, colorless to faintly yellow

SMILES 字串

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

InChI

1S/C6H8N2O3/c1-7-4(9)3-5(10)8(2)6(7)11/h3H2,1-2H3

InChI 密鑰

VVSASNKOFCZVES-UHFFFAOYSA-N

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相關類別

一般說明

1，3-二甲基巴比妥酸（1，3-二甲基-2，4，6（1H，3H，5H）-嘧啶三酮）是活性亚甲基化合物。它经历空心 Pd6 水溶性笼，与芘-1-甲醛，[{（tmen）Pd} 6（timb）4]（NO3）12（tmen =N,N,N′,N′-四甲基乙二胺，timb = 1，3，5-tris （1-咪唑基）苯）催化的诺文葛尔缩合反应。[1]它经过自分选的 Pd7 分子舟实验，其与各种芳香醛，具有内部纳米腔（催化剂）辅助的诺文葛尔缩合反应。[1]它通过 1，3-二甲基脲、丙二酸和乙酸酐在乙酸中反应合成。它广泛用于合成各种合成中间体和杂环化合物。[2]

應用

1，3-二甲基巴比妥酸可用于以下研究：
  • 具有五个立体中心的异色烯嘧啶二酮衍生物的对映选择性合成，通过一锅式迈克尔-诺文葛尔缩合-反电子-需要杂-狄尔斯-阿尔德反应。[3]
  • 5-芳基-6-（烷基 - 或芳基 - 氨基）-1，3-二甲基呋喃[2，3-d]嘧啶衍生物的合成。[4]
  • 微波促进醇的间接官能化，通过使用顺序一锅式 Ir（III）/Pd（0） 催化过程的螺环化。[5]

象形圖

CorrosionExclamation mark
GHS05,GHS07

訊號詞

Danger

危險聲明

H302,H318

危險分類

Acute Tox. 4 Oral - Eye Dam. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 1

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
WXBF5304V
WXBF4949V
WXBF3419V
WXBF4111V
WXBF3992V

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Argintaru OA.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2011)
Christian Löfberg et al.
Chemical communications (Cambridge, England), (48)(48), 5000-5002 (2006-12-06)
Microwave assisted indirect functionalization of alcohols with 1,3-dimethylbarbituric acid followed by spirocyclisation employing a sequential one-pot Ir(III)/Pd(0) catalysed process, involving the formation of three new C-C bonds, one spirocyclic ring and one di- or tri-substituted exocyclic alkene, is described.
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Electrochemical oxidation of trimipramine in the absence and presence of 1,3 dimethyl barbituric acid as a nucleophile in aqueous solution has been studied using cyclic voltammetry and controlled-potential coulometry electrolysis. Voltammetric studies of electro-oxidation of trimipramine were realized in a
María Victoria Roux et al.
The journal of physical chemistry. A, 115(14), 3167-3173 (2011-03-25)
This paper reports an experimental and computational thermochemical study on 1,3-dimethylbarbituric acid. The value of the standard (p° = 0.1 MPa) molar enthalpy of formation in the gas phase at T = 298.15 K has been determined. The energy of
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5-Aryl-6-(alkyl- or aryl-amino)-1,3-dimethylfuro [2,3-d]pyrimidine derivatives were obtained by in situ reaction alkyl or aryl isocyanides and pyridinecarbaldehyde derivatives in the presence of 1,3-dimethylbarbituric acid in dichloromethane without any prior activation or modifications.
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