V900075
巴比妥酸
Vetec™, reagent grade, 98%
别名:
2,4,6-三羟基嘧啶, 丙二酰脲
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经验公式（希尔记法）:
C4H4N2O3
化学文摘社编号:
分子量:
128.09
EC Number:
200-658-0
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
120502
InChI
1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
InChI key
HNYOPLTXPVRDBG-UHFFFAOYSA-N
SMILES string
O=C1CC(=O)NC(=O)N1
grade
reagent grade
product line
Vetec™
assay
98%
mp
248-252 °C (dec.) (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
法规信息
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Accurately predicting in vivo metabolic clearance from in vitro liver microsomes or hepatocytes requires a good understanding of the factors contributing to the prediction. Although much work has concentrated on deriving scaling factors and optimizing the metabolic stability techniques for
Roberta P Glick et al.
Pediatric neurosurgery, 47(2), 152-157 (2011-09-22)
In the pediatric population, treatment of severely injured children presenting with low Glasgow Coma Score (GCS) and fixed and dilated pupils is controversial. The combination of barbiturate coma and decompressive craniectomy as an aggressive means of controlling intracranial pressure is
Xiao-Feng Xia et al.
Chemistry, an Asian journal, 7(7), 1538-1541 (2012-04-11)
An efficient method to construct cyclopenta[c]chromene skeletons by Lewis acid-catalyzed intramolecular [3+2] cycloaddition of cyclopropane 1,1-diesters with alkynes is presented. Two new fused cycles can be formed in one step in moderate to excellent yields (up to 94 %), and the
Anik Sen et al.
Angewandte Chemie (International ed. in English), 51(45), 11279-11283 (2012-10-06)
Crystal face lift: barbituric acid is shown to be a new crystal-habit modifier for sodium chloride crystals. Two morphologies of salt crystals can be prepared separately with this new additive. It is of the few additives able to induce rhombic
Biswajita Baruah et al.
Molecular diversity, 16(2), 291-298 (2012-02-03)
Reaction of barbituric acids with aldehydes and dihydropyridines in one pot under microwave (MW) irradiation in the absence of solvent, affords 55–82% of the 5-benzylated barbituric acids. Use of alkyl nitriles or barbituric acids with indole-3-aldehyde and dihydropyridine (DHP) afforded
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