143936
丙酰胺
97%
别名:
Propanamide, 正丙酰胺
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线性分子式:
CH3CH2CONH2
化学文摘社编号:
分子量:
73.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-172-1
MDL number:
Assay:
97%
产品名称
丙酰胺, 97%
InChI key
QLNJFJADRCOGBJ-UHFFFAOYSA-N
InChI
1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5)
SMILES string
CCC(N)=O
assay
97%
bp
213 °C (lit.)
mp
76-79 °C (lit.)
solubility
alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble
water: freely soluble
density
1.042 g/mL at 25 °C (lit.)
functional group
amide
Quality Level
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Application
丙酰胺在测定乙酰胺和丙酰胺在多壁碳纳米管上的吸附等温线时可用作吸附剂。它已被用于一种可靠的筛选方法来研究使用(+)-γ-内酰胺酶的生物转化。
General description
γ-辐射中的丙酰胺可与二氧化硫反应，而且该研究已通过ESR光谱、气体吸收测量和X射线衍射进行了研究。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Study of Adsorption Isotherms of Acetamide and Propionamide on Carbon Nanotube.
Vadi M and Moradi N.
Orient. J. Chem., 27(4), 1491-1491 (2011)
R X Xu et al.
Biochemistry, 33(4), 907-916 (1994-02-01)
The oxidation of Co(II) bleomycin A2 by dioxygen leads to two products, HO2-Co(III) bleomycin A2 (form I) and Co(III) bleomycin A2 (form II). 1H NMR chemical shift assignments for protons of both forms have been made by two-dimensional NMR spectral
David Crich et al.
The Journal of organic chemistry, 74(9), 3389-3393 (2009-04-25)
Beta-thiolactones monosubstituted in the 3-position by alkyl and carbamoyl groups undergo nucleophilic ring opening by arenethiolates through a process involving an S(N)2-type attack at the 4-position leading to 3-arylthiopropionates substituted in the 2-position. These thiocarboxylates can be trapped in situ
Nobuhito Yukuhiro et al.
Brain research, 1027(1-2), 59-66 (2004-10-21)
We investigated the effects of (S)-N-[2-(1,6,7,8-tetrahydro-2H-indeno-[5,4]furan-8-yl)ethyl]propionamide (ramelteon, TAK-375), a novel MT1/MT2 receptor agonist, on nocturnal sleep in freely moving monkeys and compared these results with those of melatonin and zolpidem. Treatment with ramelteon (0.03 and 0.3 mg/kg, p.o.) significantly shortened
Tiia Kuuranne et al.
Drug metabolism and disposition: the biological fate of chemicals, 36(3), 571-581 (2007-12-19)
Selective androgen receptor modulators (SARM) are a prominent group of compounds for being misused in sports owing to their advantageous anabolic properties and reduced side effects. To target the preventive doping control analysis in relevant compounds, the challenge is to
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