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About This Item
经验公式（希尔记法）:
C12H11NO2
CAS号:
分子量:
201.22
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
化驗
97%
bp
120 °C/0.4 mmHg (lit.)
mp
63-67 °C (lit.)
SMILES 字串
CCOC(=O)c1cnc2ccccc2c1
InChI
1S/C12H11NO2/c1-2-15-12(14)10-7-9-5-3-4-6-11(9)13-8-10/h3-8H,2H2,1H3
InChI 密鑰
OTTDACPMYLDVTL-UHFFFAOYSA-N
一般說明
Ethyl 3-quinolinecarboxylate can be prepared from 3-quinolinecarboxylic acid by treating with thionyl chloride followed by esterification with ethanol. Its photochemical reaction in various alcohols and cyclohexane show that the nature of the solvent has an impact on the product formation.
應用
Ethyl 3-quinolinecarboxylate may be used as a starting material in the preparation of 5-quinolinemethanol and ethyl 3-quinolineacetate.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Biosynthesis of Penicillins. VI. N-2-Hydroxyethylamides of Some Polycyclic and Heterocyclic Acetic Acids as Precursors1.
Jones RG, et al.
Journal of the American Chemical Society, 70(9), 2843-2848 (1948)
Photochemical reactions of ethoxycarbonyl-substituted quinolines.
Ono I and Hata N.
Bulletin of the Chemical Society of Japan, 60(8), 2891-2897 (1987)
QUINOLINEMETHANOLS1.
Kaslow CE and Clark WR.
The Journal of Organic Chemistry, 18(1), 55-58 (1953)
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