C115002
环戊胺
99%
别名:
氨基环戊烷
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线性分子式:
C5H9NH2
化学文摘社编号:
分子量:
85.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-697-3
Beilstein/REAXYS Number:
635706
MDL number:
Assay:
99%
Form:
liquid
产品名称
环戊胺, 99%
InChI key
NISGSNTVMOOSJQ-UHFFFAOYSA-N
InChI
1S/C5H11N/c6-5-3-1-2-4-5/h5H,1-4,6H2
SMILES string
NC1CCCC1
assay
99%
form
liquid
refractive index
n20/D 1.450 (lit.)
bp
106-108 °C (lit.)
density
0.863 g/mL at 25 °C (lit.)
Quality Level
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Application
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]。
General description
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。
signalword
Danger
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Skin Sens. 1
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
52.7 °F - closed cup
flash_point_c
11.5 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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
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.
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
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