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經驗公式(希爾表示法):
C6H7NO
CAS號碼:
分子量::
109.13
Beilstein:
508342
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
98%
bp
102-106 °C/0.25 mmHg (lit.)
mp
54-58 °C (lit.)
SMILES 字串
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 密鑰
DDUFYKNOXPZZIW-CRCLSJGQSA-N
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訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Skin Sens. 1
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
230.0 °F - closed cup
閃點(°C)
110 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Vasu Nair et al.
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
Patricia Écija et al.
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.
Steven, J. C.
Journal of the Chemical Society. Chemical Communications, 16, 1120-1121 (1990)
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