4'-Iodoacetophenone - ≥98% , CAS No.13329-40-3

CAS: 13329-40-3 Cat. No.: I107027 Formula: C₈H₇IO Peso molecolare: 246.05 Beilstein Registry Number: 7(3)989 Numero EC: 236-372-8

GRADE & PURITY ≥98%

Synonyms

4-iodophenyl methyl ketone | 1-(4-Iodophenyl)ethan-1-one | NSC 97396 | 4/'-Iodoacetophenone | EINECS 236-372-8 | Fluonex | BCP22400 | Ethanone, 1-(4-iodophenyl)- | InChI=1/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H | perfluorohexanes | 4 inverted exclamation

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinonimi

4-iodophenyl methyl ketone | 1-(4-Iodophenyl)ethan-1-one | NSC 97396 | 4/'-Iodoacetophenone | EINECS 236-372-8 | Fluonex | BCP22400 | Ethanone, 1-(4-iodophenyl)- | InChI=1/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H | perfluorohexanes | 4 inverted exclamation

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 504754672
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754672
• Sorrisi canonici: CC(=O)C1=CC=C(C=C1)I
• IUPAC Name: 1-(4-iodophenyl)ethanone
• InChIKey: JZJWCDQGIPQBAO-UHFFFAOYSA-N
• INCHI: 1S/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3
• Isomeri SMILES: CC(=O)C1=CC=C(C=C1)I
• WGK Germania: 3
• Peso molecolare: 246.05
• Beilstein: 7(3)989
• Reaxy-Rn: 1857412
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1857412&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Ketones
          • Level6 Aryl ketones
            • Level7 Phenylketones
              • Level8 Alkyl-phenylketones

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Ketones - Aryl ketones - Phenylketones
• Direct Parent: Alkyl-phenylketones
• Alternative Parents: Acetophenones Benzoyl derivatives Aryl alkyl ketones Iodobenzenes Aryl iodides Organoiodides Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alkyl-phenylketone - Acetophenone - Aryl alkyl ketone - Benzoyl - Iodobenzene - Halobenzene - Benzenoid - Monocyclic benzene moiety - Aryl iodide - Aryl halide - Organic oxide - Hydrocarbon derivative - Organoiodide - Organohalogen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Solubilità: Easily soluble in water.
• Sensibilità: Light sensitive.
• Punto di fusione (°C): 82-84°C
• Peso molecolare: 246.040 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 245.954 Da
• Monoisotopic Mass: 245.954 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 125.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Yanqi Ban, Hui Wang, Zixuan Xiao, Lishui Sun, Qingyan Pan, Yingjie Zhao.  (2023)  Interfacial Synthesis of an Ultrathin Two-Dimensional Polymer Film via [2 + 2] Photocycloaddition.  MOLECULES,  28  (4): (1930).  [PMID:36838919] [10.3390/molecules28041930]