产品名称
4-氟吲哚, 97%
InChI
1S/C8H6FN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H
SMILES string
Fc1cccc2[nH]ccc12
InChI key
ZWKIJOPJWWZLDI-UHFFFAOYSA-N
assay
97%
bp
90 °C/0.4 mmHg (lit.)
mp
30-32 °C (lit.)
functional group
fluoro
Application
- 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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Journal of the Chemical Society. Perkin Transactions 1, 1765-1765 (1994)
Synthesis of (L)-4-Fluorotryptophan.
Konas DW, et al.
Synthetic Communications, 42(1), 144-152 (2012)
(Erratum)
Journal of Medicinal Chemistry, 2442-2442 null
A synthesis of (-)-indolactam V.
Semmelhack MF and Rhee H.
Tetrahedron Letters, 34(39), 1395-1398 (1993)
4-Fluoroindole and Derivatives.
Bentov M, et al.
Israel J. Chem., 2(1), 25-28 (1964)
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