Weight | 168.167 g/mol |
---|---|
Formula | C9H9FO2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
2-(4-fluorophenyl)propanoic acid (75908-73-5)
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- Operationally convenient asymmetric synthesis of (S)-2-amino-3,3-bis-(4-fluorophenyl)propanoic acid (Journal of Fluorine Chemistry, 2009)
- Design and Synthesis of 3-(2-Ethyl-4-{2-[2-(4-fluorophenyl)-5-methyloxazol-4-yl]ethoxy}phenyl)propanoic Acid: A Novel Triple-acting PPAR, -, and - Agonist (Chemistry Letters, 2012)
- Thermodynamically resistant form of (r)-3-[[(4-fluorophenyl)- sulfonyl]amino]-1,2,3,4-tetrahydro-9h-carbazole-9-propanoic acid (ramatroban) (1998)
- Thermodynamisch stabile Form von (r)-3[[(4-Fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-0-propansure (Ramatroban) Thermodynamically stable form of (R) -3 [[(4-fluorophenyl) sulfonyl] amino] -1,2,3,4-tetrahydro-9H-carbazol-0-propanoic acid (ramatroban) (1997)
- Thermodynamically stable form of (r)-3-[ [(4-fluorophenyl) sulphonyl]amino] -1,2,3,4- tetrahydro -9h-carbazole -9-propanoic acid (ramatroban) (1998)
- Thermodynamically stable form of (R)-3-&lsqb &lsqb (4-fluorophenyl) sulphonyl&rsqb amino&rsqb -1,2,3,4-tetrahydro-9H-carbazole-9-propanoic acid (ramatroban) (2002)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C1=CC=C(C=C1)F)C(=O)O
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InChIKeyIXSCGBODJGIJNN-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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