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质量水平
方案
99%
表单
liquid
折射率
n20/D 1.450 (lit.)
沸点
106-108 °C (lit.)
密度
0.863 g/mL at 25 °C (lit.)
SMILES字符串
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
Room-temperature ABX 3-typed molecular ferroelectric:[C 5 H 9-NH 3][CdCl 3]
Inorganic chemistry frontiers, 1, 118-123 (2014)
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
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
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.
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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