A39300
4-氨基安替比林
98%
别名:
4-氨基-2,3-二甲基-1-苯基-3-吡唑啉-5-酮, 氨基安替比林
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关于此项目
经验公式（希尔记法）:
C11H13N3O
化学文摘社编号:
分子量:
203.24
EC Number:
201-452-3
UNSPSC Code:
12352103
MDL number:
Beilstein/REAXYS Number:
181635
产品名称
4-氨基安替比林, 98%
InChI
1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3
InChI key
RLFWWDJHLFCNIJ-UHFFFAOYSA-N
SMILES string
CN1N(c2ccccc2)C(=O)C(N)=C1C
assay
98%
mp
105-110 °C (lit.)
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Application
该试剂用于比色测定酚类，以及合成过渡金属和镧系配体。
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Analytical Letters, 26, 87-87 (1993)
Transition Met. Chem. (London), 18, 279-279 (1993)
Polyhedron, 12, 1227-1227 (1993)
Qihui Wang et al.
Journal of hazardous materials, 186(2-3), 1076-1081 (2010-12-21)
In this work, the immobilization of 4-aminoantipyrine onto bentonite was carried out and it was then used to investigate the adsorption behavior of Cr(III), Hg(II) and Pb(II) ions from aqueous solutions. The separation and preconcentration conditions of analytes were investigated
Mohammad Sayed Alam et al.
Bioorganic & medicinal chemistry, 20(13), 4103-4108 (2012-05-26)
4-Aminoantipyrine (4-amino-1,5-dimethyl-2-phenylpyrazole-3-one) and its analogues have been found to be compounds of interest for their anti-inflammatory, analgesic, antiviral, antipyretic, antirheumatic and antimicrobial activities. In the present study, Schiff base analogues of 4-aminoantipyrine were synthesized by the condensation reaction with substituted
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