产品名称
巴比妥酸, ReagentPlus®, 99%
Quality Level
product line
ReagentPlus®
assay
99%
form
powder
mp
248-252 °C ((lit.)), 248-252 °C (dec.) (lit.)
SMILES string
[O=C1CC(=O)NC(=O)N1], O=C1CC(=O)NC(=O)N1
InChI
[1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)], 1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
InChI key
[HNYOPLTXPVRDBG-UHFFFAOYSA-N], HNYOPLTXPVRDBG-UHFFFAOYSA-N
General description
巴比妥酸适用于有机和药物合成。其二水合物形式可以由巴比妥酸通过从水溶液中结晶合成。研究人员已通过三维傅里叶变换法,对巴比妥酸(呈互变异构形式)的晶体结构进行了研究。据报道,它的烯醇晶体形式为热力学稳定形式。
Application
它可能用于合成:
- 5-亚基巴比妥酸衍生物(通过与芳香醛和α,β-共轭芳香醛进行Knoevenagel缩合)
- 5-二氨基亚甲基巴比妥酸盐(通过与取代的碳二亚胺反应)
通过SmI2/H2O试剂存在下的化学选择性还原,巴比妥酸(BA)可用于制备相应的半胺醛。它可用于制备BA-改性的共轭氮化碳纳米片。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
302.0 °F - closed cup
flash_point_c
150.00 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Selective reduction of barbituric acids using SmI2/H2O: synthesis, reactivity, and structural analysis of tetrahedral adducts.
Michal Szostak et al.
Angewandte Chemie (International ed. in English), 52(48), 12559-12563 (2013-10-15)
A simple method for knoevenagel condensation of a, ?-conjugated and aromatic aldehydes with barbituric acid.
Jursic BS.
Journal of Heterocyclic Chemistry, 38(3), 655-657 (2001)
Photocatalytic reduction of CO2 by graphitic carbon nitride polymers derived from urea and barbituric acid.
Qin J, et al.
Applied Catalysis. B, Environmental, 179, 1-8 (2015)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 185698-100G | 04061835252831 |
| 185698-500G | 04061835252855 |
| 185698-25G | 04061835252848 |