00370
对乙酰氨基酚
purum, ≥98.0% (HPLC)
别名:
4′-羟基乙酰苯胺, 4-乙酰氨基酚, N-(4-羟基苯基)乙酰胺, N-乙酰基-4-氨基苯酚, APAP, 扑热息痛
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关于此项目
线性分子式:
CH3CONHC6H4OH
化学文摘社编号:
分子量:
151.16
EC Number:
203-157-5
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
2208089
grade
purum
assay
≥98.0% (HPLC)
ign. residue
≤0.5%
mp
168-172 °C
SMILES string
CC(=O)Nc1ccc(O)cc1
InChI
1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)
InChI key
RZVAJINKPMORJF-UHFFFAOYSA-N
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Application
镇痛剂。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
364.3 °F - Pensky-Martens closed cup
flash_point_c
184.6 °C - Pensky-Martens closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Christian Sinning et al.
Journal of medicinal chemistry, 51(24), 7800-7805 (2008-12-05)
N-(4-hydroxyphenyl)-(5Z,8Z,11Z,14Z)-icosatetra-5,8,11,14-enamide (AM404) is a metabolite of the well-known analgesic paracetamol. AM404 inhibits endocannabinoid cellular uptake, binds weakly to CB1 and CB2 cannabinoid receptors, and is formed by fatty acid amide hydrolase (FAAH) in vivo. We prepared three derivatives of this
Anthony L Vaccarino et al.
Bioorganic & medicinal chemistry, 15(5), 2206-2215 (2006-08-22)
A series of acetaminophen (APAP) analogs, 2-(1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)-N-(4-hydroxyphenyl)alkanecarboxamides, bearing a heterocyclic moiety linked to the p-acylaminophenol fragment, were prepared in a general project to develop APAP analogs with modulated pharmacokinetic profiles. Unexpectedly, the products described maintained the in vivo analgesic profile
Wolfgang Friebolin et al.
Journal of medicinal chemistry, 51(5), 1260-1277 (2008-02-12)
Plasmodium parasites are exposed to higher fluxes of reactive oxygen species and need high activities of intracellular antioxidant systems providing a steady glutathione flux. As a future generation of dual drugs, 18 naphthoquinones and phenols (or their reduced forms) containing
Susruta Majumdar et al.
Bioorganic & medicinal chemistry letters, 16(13), 3590-3594 (2006-04-18)
Synthesis, characterization and hydrolysis in aqueous buffers of novel N-alkyl-N-alkyloxycarbonylaminomethyl (NANAOCAM) derivatives of substituted phenols, theophylline (Th) and 6-mercaptopurine (6MP) were carried out. The mechanism of hydrolysis was further investigated by synthesis, characterization and hydrolysis of N-aryl-N-alkyloxycarbonylaminomethyl (NArNAOCAM) derivatives of
Microsomal prostaglandin E2 synthase-1 (mPGES-1): a novel anti-inflammatory therapeutic target.
Richard W Friesen et al.
Journal of medicinal chemistry, 51(14), 4059-4067 (2008-05-08)
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