Merck
CN

C115002

Sigma-Aldrich

环戊胺

99%

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别名:
氨基环戊烷
线性分子式:
C5H9NH2
CAS号:
分子量:
85.15
Beilstein:
635706
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

liquid

折射率

n20/D 1.450 (lit.)

bp

106-108 °C (lit.)

密度

0.863 g/mL at 25 °C (lit.)

SMILES string

NC1CCCC1

InChI

1S/C5H11N/c6-5-3-1-2-4-5/h5H,1-4,6H2

InChI key

NISGSNTVMOOSJQ-UHFFFAOYSA-N

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一般描述

环庚胺是多功能化合物,在有机合成中应用广泛。可充当合成砌块、催化剂和反应剂,是研发新有机物的宝贵工具。还可用作有机分子的官能化试剂。

应用

环庚胺可作为合成砌块制备ABX3型钙钛矿结构化合物[C5H9–NH3][CdCl3]。

警示用语:

Danger

危险分类

Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Skin Sens. 1

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

52.7 °F - closed cup

闪点(°C)

11.5 °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

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D G Craciunescu et al.
In vivo (Athens, Greece), 1(4), 229-234 (1987-07-01)
Ten new Pt (II) complexes were synthesized and tested as potential antitumor drugs in vitro on KB human tumour cell line, and in vivo against four experimental tumour systems (P388, L1210, ADJ/PC6A and Yoshida sarcoma). The complexes contained two primary
M J Comin et al.
Nucleosides & nucleotides, 18(10), 2219-2231 (2000-01-05)
Purine carbanucleosides built on a 6-oxabicyclo[3.1.0]hexane template were synthesized from readily available 2-cyclopentenone employing a Mitsunobu reaction to incorporate the base onto the carbocyclic ring. Both adenosine and guanosine analogues exhibited moderate antiviral activity.
M S Sansom et al.
Protein engineering, 6(1), 65-74 (1993-01-01)
The influenza A M2 protein forms cation-selective ion channels which are blocked by the anti-influenza drug amantadine. A molecular model of the M2 channel is presented in which a bundle of four parallel M2 transbilayer helices surrounds a central ion-permeable
Room-temperature ABX 3-typed molecular ferroelectric:[C 5 H 9-NH 3][CdCl 3]
Zhang, Yi and Ye, et al.
Inorganic chemistry frontiers, 1, 118-123 (2014)
Maris Vilums et al.
Journal of medicinal chemistry, 56(19), 7706-7714 (2013-09-14)
Preclinical models of inflammatory diseases (e.g., neuropathic pain, rheumatoid arthritis, and multiple sclerosis) have pointed to a critical role of the chemokine receptor 2 (CCR2) and chemokine ligand 2 (CCL2). However, one of the biggest problems of high-affinity inhibitors of

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