质量水平
方案
98%
表单
liquid
折射率
n20/D 1.432 (lit.)
沸点
61-62 °C (lit.)
密度
0.847 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
C1CNC1
InChI
1S/C3H7N/c1-2-4-3-1/h4H,1-3H2
InChI key
HONIICLYMWZJFZ-UHFFFAOYSA-N
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一般描述
本文研究了氮杂环丁烷自由基丁烷自由基阳离子在λ= 436 nm的光作用下的光化反应。测定了氮杂环丁烷在固体氩基质中的红外光谱。
应用
氮杂环丁烷用于：
- 高产率钯催化与芳基溴化物的交叉偶联反应
- 碘硝基阳离子的Ullmann型偶联反应
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
-4.0 °F
闪点(°C)
-20 °C
个人防护装备
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
Phototransformations of azetidine radical cations stabilized in freonic matrices.
Sorokin ID, et al.
High Energy Chemistry, 48(3), 180-184 (2014)
Experimental and computational studies of the structure and vibrational spectra of azetidine derivatives.
Thompson CA, et al.
Journal of Molecular Structure, 491(1), 67-80 (1999)
Synthesis, 243-243 (2007)
Asta Žukauskaitė et al.
Amino acids, 41(3), 541-558 (2011-03-23)
A short synthesis of alkyl 2-(bromomethyl)aziridine-2-carboxylates and alkyl 3-bromoazetidine-3-carboxylates was developed involving amination, bromination, and base-induced cyclization of alkyl 2-(bromomethyl)acrylates. The aziridines are the kinetically favored cyclization products and could be transformed into 3-bromoazetidine-3-carboxylic acid derivatives via thermal isomerization. The
Alan P Kozikowski et al.
ChemMedChem, 4(8), 1279-1291 (2009-07-02)
AMOP-H-OH (sazetidine-A; 6-[5-(azetidin-2-ylmethoxy)pyridin-3-yl]hex-5-yn-1-ol) and some sulfur-bearing analogues were tested for their activities in vitro against human alpha4beta2-, alpha4beta4-, alpha3beta4*- and alpha1*-nicotinic acetylcholine receptors (nAChRs). AMOP-H-OH was also assessed in an antidepressant efficacy model. AMOP-H-OH and some of its analogues have
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