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关于此项目
经验公式(希尔记法):
C3H7N
化学文摘社编号:
分子量:
57.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-963-8
Beilstein/REAXYS Number:
102384
MDL number:
Assay:
98%
Form:
liquid
InChI key
HONIICLYMWZJFZ-UHFFFAOYSA-N
InChI
1S/C3H7N/c1-2-4-3-1/h4H,1-3H2
SMILES string
C1CNC1
assay
98%
form
liquid
refractive index
n20/D 1.432 (lit.)
bp
61-62 °C (lit.)
density
0.847 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
General description
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。
Application
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
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-4.0 °F
flash_point_c
-20 °C
ppe
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
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)
Phototransformations of azetidine radical cations stabilized in freonic matrices.
Sorokin ID, et al.
High Energy Chemistry, 48(3), 180-184 (2014)
Synthesis, 243-243 (2007)
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
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
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