Cas no 81028-92-4 (3-(3,5-Dichlorophenoxy)benzaldehyde)

3-(3,5-Dichlorophenoxy)benzaldehyde structure
81028-92-4 structure
Product Name:3-(3,5-Dichlorophenoxy)benzaldehyde
CAS No:81028-92-4
MF:C13H8Cl2O2
MW:267.107421875
MDL:MFCD00003355
CID:728116
PubChem ID:24851845
Update Time:2024-10-27

3-(3,5-Dichlorophenoxy)benzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-(3,5-Dichlorophenoxy)benzaldehyde
    • Benzaldehyde,3-(3,5-dichlorophenoxy)-
    • 3-(3,5-Dichorophenoxy)benzaldehyde
    • m-(3,5-Dichlorophenoxy)benzaldehyde
    • Benzaldehyde, 3-(3,5-dichlorophenoxy)-
    • PubChem16379
    • BISWHYILBVQCRA-UHFFFAOYSA-N
    • KM2057
    • OR5240
    • 3-(3?5-Dichlorophenoxy)benzaldehyde
    • SC3781
    • SBB003061
    • 3-(3,5-dichlorophenoxy)-benzaldehyde
    • 3-(3,5-Dichlorophenoxy)benzaldehyde (ACI)
    • 3-(3,5-Dichlorophenoxybenzaldehyde
    • [3-(3,5-Dichlorophenoxy)phenyl]formaldehyde
    • J-510577
    • AC-7932
    • EINECS 279-661-4
    • AKOS009158571
    • SY011762
    • 3-(3,5-Dichlorophenoxy)benzaldehyde, 95%
    • 81028-92-4
    • DTXSID501001717
    • NS00059834
    • CS-W010113
    • BP-12413
    • SCHEMBL414827
    • PS-7309
    • MFCD00003355
    • MDL: MFCD00003355
    • Inchi: 1S/C13H8Cl2O2/c14-10-5-11(15)7-13(6-10)17-12-3-1-2-9(4-12)8-16/h1-8H
    • InChI Key: BISWHYILBVQCRA-UHFFFAOYSA-N
    • SMILES: O=CC1C=C(OC2C=C(Cl)C=C(Cl)C=2)C=CC=1

Computed Properties

  • Exact Mass: 265.99000
  • Monoisotopic Mass: 265.99
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3
  • Complexity: 250
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4.6
  • Topological Polar Surface Area: 26.3
  • Surface Charge: 0
  • Tautomer Count: nothing

Experimental Properties

  • Color/Form: solid
  • Density: 1.3001 (rough estimate)
  • Melting Point: 48-55?°C (lit.)
  • Boiling Point: 125?°C/0.03?mmHg(lit.)
  • Flash Point: Degrees Fahrenheit:>235.4°F
    Degrees Celsius:>113°C
  • Refractive Index: 1.4730 (estimate)
  • PSA: 26.30000
  • LogP: 4.59820
  • Solubility: Not determined
  • Vapor Pressure: 0.0±0.9 mmHg at 25°C

3-(3,5-Dichlorophenoxy)benzaldehyde Security Information

3-(3,5-Dichlorophenoxy)benzaldehyde Customs Data

  • HS CODE:2913000090
  • Customs Data:

    China Customs Code:

    2913000090

    Overview:

    2913000090 Item2912Other derivatives of the listed products [refer to halogenation,sulfonation,Nitrosative or nitrosative derivatives]. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

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3-(3,5-Dichlorophenoxy)benzaldehyde Production Method

Production Method 1

Reaction Conditions
1.1 Catalysts: Cupric acetate
Reference
Cinnamonitrile Adjuvants Restore Susceptibility to β-Lactams against Methicillin-Resistant Staphylococcus aureus
Speri, Enrico ; et al, ACS Medicinal Chemistry Letters, 2019, 10(8), 1148-1153

Production Method 2

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Tetrahydrofuran ,  Water ;  2 - 7 h, rt
Reference
Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors
Song, Lijun; et al, European Journal of Medicinal Chemistry, 2021, 225,

Production Method 3

Reaction Conditions
1.1 Reagents: Cesium carbonate ,  Oxygen Catalysts: Dimethylglycine hydrochloride ,  Cuprous iodide Solvents: 1,4-Dioxane ;  24 h, 90 °C
1.2 Reagents: Hydrochloric acid Solvents: Tetrahydrofuran ,  Water ;  2 - 7 h, rt
Reference
Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors
Song, Lijun; et al, European Journal of Medicinal Chemistry, 2021, 225,

Production Method 4

Reaction Conditions
1.1 Reagents: Acetic anhydride ,  Pyridine ;  0 °C; 1 h, rt
1.2 Reagents: Sodium chloride Solvents: Water ;  0 °C
1.3 Solvents: Toluene ;  2 h, reflux; reflux → rt
1.4 Reagents: Sodium hydroxide Solvents: Water ;  2 h, rt
1.5 Reagents: Hydrochloric acid Solvents: Water ;  pH 8, rt
2.1 Reagents: Cesium carbonate ,  Oxygen Catalysts: Dimethylglycine hydrochloride ,  Cuprous iodide Solvents: 1,4-Dioxane ;  24 h, 90 °C
2.2 Reagents: Hydrochloric acid Solvents: Tetrahydrofuran ,  Water ;  2 - 7 h, rt
Reference
Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors
Song, Lijun; et al, European Journal of Medicinal Chemistry, 2021, 225,

3-(3,5-Dichlorophenoxy)benzaldehyde Raw materials

3-(3,5-Dichlorophenoxy)benzaldehyde Preparation Products

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