化驗
97%
bp
90 °C/0.4 mmHg (lit.)
mp
30-32 °C (lit.)
官能基
fluoro
SMILES 字串
Fc1cccc2[nH]ccc12
InChI
1S/C8H6FN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H
InChI 密鑰
ZWKIJOPJWWZLDI-UHFFFAOYSA-N
應用
- Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
- Reactant for preparation of antifungal agents
- Reactant for preparation of Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the Management of Hyperglycemia in Diabetes
- Reactant for preparation of Potent Selective Serotonin Reuptake Inhibitors
- Reactant for preparation of Inhibitors of HIV-1 attachment
- Reactant for preparation of monoamine reuptake inhibitors
- Reactant for preparation of histone deacetylase (HDAC) inhibitors
- Reactant for preparation of inhibitors of proliferation of human breast cancer cells
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
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
(Erratum)
Journal of Medicinal Chemistry, 2442-2442 null
Synthesis of (L)-4-Fluorotryptophan.
Konas DW, et al.
Synthetic Communications, 42(1), 144-152 (2012)
Journal of the Chemical Society. Perkin Transactions 1, 1765-1765 (1994)
J L Malleron et al.
Journal of medicinal chemistry, 36(9), 1194-1202 (1993-04-30)
A series of new indole derivatives (2-28) has been prepared in the search for novel 5-HT uptake inhibitors. These compounds were obtained by the condensation of N-(chloroalkyl) naphthalenesultam derivatives with the appropriate amine in presence of a base, at reflux
A synthesis of (-)-indolactam V.
Semmelhack MF and Rhee H.
Tetrahedron Letters, 34(39), 1395-1398 (1993)
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