529036
3-Iodobenzonitrile
98%
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About This Item
Formula condensata:
IC6H4CN
Numero CAS:
Peso molecolare:
229.02
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Saggio
98%
Punto di fusione
40-43 °C (lit.)
Stringa SMILE
Ic1cccc(c1)C#N
InChI
1S/C7H4IN/c8-7-3-1-2-6(4-7)5-9/h1-4H
BGARPMGQRREXLN-UHFFFAOYSA-N
Descrizione generale
3-Iodobenzonitrile is a halogenated aromatic nitrile. Its standard (ρ° = 0.1MPa) molar enthalpy of formation was determined by combustion calorimetry.
Applicazioni
3-Iodobenzonitrile may be used as a starting reagent in the synthesis of tetrachloroisophthalo-[14C]-nitrile (TCIN). It may also be used in the preparation of:
- 1-(3-iodophenyl)-3-{2-[4-(trifluoromethyl)-1-piperidinyl]ethyl}-2-imidazolidinone
- piperidine derivative
- chiral amino acid anilide
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
230.0 °F - closed cup
Punto d’infiammabilità (°C)
110 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
Certificati d'analisi (COA)
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
Thermodynamic and aromaticity studies for the assessment of the halogen? cyano interactions on Iodobenzonitrile.
Rocha IM, et al.
The Journal of Chemical Thermodynamics, 65, 204-212 (2013)
Synthesis of Chiral Amino Acid Anilides by Ligand-Free Copper-Catalyzed Selective N-Arylation of Amino Acid Amides
Dong J, et al.
Advanced Synthesis & Catalysis, 355(4), 692-696 (2013)
Idriss Bennacef et al.
Bioorganic & medicinal chemistry letters, 19(17), 5056-5059 (2009-07-29)
Compound 1 is a potent and selective antagonist of the dopamine D(3) receptor. With the aim of developing a carbon-11 labeled ligand for the dopamine D(3) receptor, 1 was selected as a potential PET probe. [(11)C]1 was obtained by palladium
Dominic P Affron et al.
European journal of organic chemistry, 2016(1), 139-149 (2016-02-16)
Saturated heterocycles, such as THFs, pyrrolidines, piperidines and THPs, are essential components of many biologically active compounds. Examples of C-H functionalization on these important ring systems remain scarce, especially at unactivated positions. Here we report the development of conditions for
Synthesis of tetrachloroisophthalo-[14C]-nitrile.
Davies PE.
Journal of Labelled Compounds & Radiopharmaceuticals, 21(3), 285-292 (1984)
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