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质量水平
方案
98%
沸点
102-106 °C/0.25 mmHg (lit.)
mp
54-58 °C (lit.)
SMILES字符串
O=C1N[C@H]2C[C@@H]1C=C2
InChI
1S/C6H7NO/c8-6-4-1-2-5(3-4)7-6/h1-2,4-5H,3H2,(H,7,8)/t4-,5+/m0/s1
InChI key
DDUFYKNOXPZZIW-CRCLSJGQSA-N
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一般描述
2-氮杂双环[2.2.1]庚-5-烯-3-酮也称为文斯内酰胺。它是碳环核苷合成中的一种通用中间体。2-氮杂双环[2.2.1]庚-5-烯-3-酮及其一元水合物已通过傅立叶变换微波光谱法在超音速飞机中进行了研究。
应用
2-氮杂双环[2.2.1]庚-5-烯-酮已被用于:
- 制备(3aS,4R,6R,6aR)-6-((甲氧基-甲氧基)甲基)-2,2-二甲基四氢-3aH-环戊[d] [1,3]二恶酚-4-胺,一种布雷迪宁类似物的前体
- 治疗性药物的合成
- (−)-卡巴韦的化学酶促合成
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
The journal of physical chemistry. A, 116(41), 10099-10106 (2012-09-19)
2-Azabicyclo[2.2.1]hept-5-en-3-one (ABH or Vince lactam) and its monohydrated complex (ABH···H(2)O) have been observed in a supersonic jet by Fourier transform microwave spectroscopy. ABH is broadly used in the synthesis of therapeutic drugs, whereas the ABH···H(2)O system offers a simple model
Chemoenzymatic synthesis of (-)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo [2.2. 1] hept-5-en-3-one.
Journal of the Chemical Society. Chemical Communications, 16, 1120-1121 (1990)
Molecules (Basel, Switzerland), 18(9), 11576-11585 (2013-09-21)
The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. While various nucleosides related to bredinin have been synthesized, its carbocyclic analog has remained unknown. Synthesis of this heretofore unknown analog of bredinin is described. The key precursor, (3aS,4R,6R,6aR)-6-((methoxy-methoxy)methyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-amine
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