Merck
CN

143936

Sigma-Aldrich

丙酰胺

97%

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别名:
Propanamide, 正丙酰胺
线性分子式:
CH3CH2CONH2
CAS号:
分子量:
73.09
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

bp

213 °C (lit.)

mp

76-79 °C (lit.)

溶解性

alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble
water: freely soluble

密度

1.042 g/mL at 25 °C (lit.)

SMILES string

CCC(N)=O

InChI

1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5)

InChI key

QLNJFJADRCOGBJ-UHFFFAOYSA-N

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此商品
3455712495488.21046
Propionamide 97%

Sigma-Aldrich

143936

丙酰胺

2-Naphthalenesulfonic acid technical grade, 70%

Sigma-Aldrich

249548

2-萘磺酸

Propionamide for synthesis

Sigma-Aldrich

8.21046

Propionamide

bp

213 °C (lit.)

bp

-

bp

-

bp

-

mp

76-79 °C (lit.)

mp

125-130 °C (lit.)

mp

-

mp

75-78 °C

solubility

alcohol: freely soluble, chloroform: freely soluble, diethyl ether: freely soluble, water: freely soluble

solubility

acetonitrile: soluble, ethanol: soluble, organic solvents: soluble, water: soluble

solubility

water: freely soluble(lit.)

solubility

-

density

1.042 g/mL at 25 °C (lit.)

density

-

density

-

density

-

一般描述

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

应用

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Reactions of Gases with Irradiated Organic Solids: III. Reactions of Propionamide, n-Butyramide, Isobutyramide, Methacrylamide, Valeramide, and Stearamide with Sulfur Dioxide.
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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
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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

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