跳转至内容
Merck
CN

P50900

Sigma-Aldrich

炔丙基胺

98%

别名:

2-丙炔胺, 3-氨基-1-丙炔

登录查看公司和协议定价

选择尺寸


关于此项目

线性分子式:
HC≡CCH2NH2
化学文摘社编号:
分子量:
55.08
Beilstein:
773681
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

质量水平

方案

98%

包含

≤2.5% water

折射率

n20/D 1.449 (lit.)

沸点

83 °C (lit.)

密度

0.86 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

NCC#C

InChI

1S/C3H5N/c1-2-3-4/h1H,3-4H2

InChI key

JKANAVGODYYCQF-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

应用

通过碳水化合物连接型氨基酸的炔丙基酰胺与 9,10-双(叠氮甲基)蒽进行 1,3-偶极环加成反应,合成手性、荧光大环类化合物。

警示用语:

Danger

危险分类

Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

42.8 °F - closed cup

闪点(°C)

6 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Synthesis, 3141-3141 (2006)
Irene Bolea et al.
Journal of neural transmission (Vienna, Austria : 1996), 120(6), 893-902 (2012-12-15)
Alzheimer's disease (AD) is a complex neurodegenerative disorder with a multifaceted pathogenesis. There are at present three Food and Drug Administration-approved drugs based on the "one drug, one target" paradigm (donepezil, galantamine and rivastigmine) that improve symptoms by inhibiting acetylcholinesterase.
Simona Pilotto et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(9), 2752-2757 (2015-03-03)
With its noncatalytic domains, DNA-binding regions, and a catalytic core targeting the histone tails, LSD1-CoREST (lysine-specific demethylase 1; REST corepressor) is an ideal model system to study the interplay between DNA binding and histone modification in nucleosome recognition. To this
Abdelouahid Samadi et al.
European journal of medicinal chemistry, 52, 251-262 (2012-04-17)
The synthesis, pharmacological evaluation and molecular modeling of heterocyclic substituted alkyl and cycloalkyl propargyl amines 1-7 of type I, and 9-12 of type II, designed as multipotent inhibitors able to simultaneously inhibit monoamine oxidases (MAO-A/B) as well as cholinesterase (AChE/BuChE)
Suyan Qiu et al.
Biosensors & bioelectronics, 26(11), 4326-4330 (2011-05-21)
Copper(I) species can be acquired from the reduction of copper(II) by ascorbic acid (AA) in situ, and which in turn quantitative catalyze the azides and alkynes cycloaddition reaction. In this study, propargyl-functionalized ferrocene (propargyl-functionalized Fc) has been modified on the

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持