528994
Ethyl-3-iodbenzoat
98%
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
98%
Brechungsindex
n20/D 1.581 (lit.)
bp
272 °C (lit.)
Dichte
1.64 g/mL at 25 °C (lit.)
Funktionelle Gruppe
ester
iodo
SMILES String
CCOC(=O)c1cccc(I)c1
InChI
1S/C9H9IO2/c1-2-12-9(11)7-4-3-5-8(10)6-7/h3-6H,2H2,1H3
InChIKey
POGCXCWRMMXDAQ-UHFFFAOYSA-N
Allgemeine Beschreibung
Ethyl 3-iodobenzoate is a halogenated aromatic ester. It affords arylzinc bromide via reaction with i-PrMgBr in THF, followed by reaction with ZnBr2.
Anwendung
Ethyl 3-iodobenzoate may be used to synthesize:
- arylzinc bromide
- functionalized arylmagnesium compound
- ethyl3-phenylbenzoate
- ethyl 3-[(12-tert-butyldimethylsilyloxymethyl-1,12-dicarba-closo-dodecaboran)-1-yl]benzoate
- ethyl 3-(4-methoxy-1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)benzoate
- ethyl 3-(1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-yl)benzoate
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
230.0 °F - closed cup
Flammpunkt (°C)
110 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Nonpeptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 2-Phenyl-4'-((2, 3, 4, 5-tetrahydro-1H-1-benzazepin-1-yl) carbonyl) benzanilide Derivatives.
Chemical & Pharmaceutical Bulletin, 45(11), 1870-1874 (1997)
Synthesis of 3, 4-Disubstituted Quinolin-2-(1H)-ones via Palladium-Catalyzed Decarboxylative Arylation Reactions.
Advanced Synthesis & Catalysis, 355(10), 2044-2054 (2013)
Bioorganic & medicinal chemistry, 17(1), 344-350 (2008-11-22)
A novel series of androgen receptor (AR) ligands bearing an acidic heterocycle with hydrogen-bonding ability as the terminal polar group was developed. Since most non-steroidal AR ligands so far known are structurally limited to nitro- or cyanobenzanilide as the polar
Copper catalyzed conjugate addition of highly functionalized arylmagnesium compounds to enones.
Tetrahedron, 56(18), 2727-2731 (2000)
Ni (II)-catalyzed cross-coupling between polyfunctional arylzinc derivatives and primary alkyl iodides.
Journal of the American Chemical Society, 120(43), 11186-11187 (1998)
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.