Cas no 93839-14-6 (2,4-Dichloro-6-methoxyaniline)

2,4-Dichloro-6-methoxyaniline structure
2,4-Dichloro-6-methoxyaniline structure
Product Name:2,4-Dichloro-6-methoxyaniline
CAS No:93839-14-6
MF:C7H7Cl2NO
MW:192.042579889297
MDL:MFCD20693704
CID:810408
PubChem ID:3022524
Update Time:2024-12-09

2,4-Dichloro-6-methoxyaniline Chemical and Physical Properties

Names and Identifiers

    • 2,4-Dichloro-6-methoxyaniline
    • Benzenamine,2,4-dichloro-6-methoxy-
    • 2,4-Dichloro-6-methoxybenzenamine
    • 6000AC
    • FCH1274322
    • AX8228428
    • 2,4-Dichloro-6-methoxybenzenamine (ACI)
    • CS-0150462
    • UNII-J64E6J8NJA
    • AKOS016009256
    • NS00039657
    • 93839-14-6
    • DTXCID40162217
    • J64E6J8NJA
    • EINECS 298-783-9
    • DTXSID90239726
    • C90753
    • NMGHEOHOYKBWEM-UHFFFAOYSA-N
    • DB-355211
    • SCHEMBL4401042
    • MFCD20693704
    • AS-59742
    • Benzenamine, 2,4-dichloro-6-methoxy-
    • MDL: MFCD20693704
    • Inchi: 1S/C7H7Cl2NO/c1-11-6-3-4(8)2-5(9)7(6)10/h2-3H,10H2,1H3
    • InChI Key: NMGHEOHOYKBWEM-UHFFFAOYSA-N
    • SMILES: ClC1C=C(OC)C(N)=C(Cl)C=1

Computed Properties

  • Exact Mass: 190.9904692g/mol
  • Monoisotopic Mass: 190.9904692g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 134
  • 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
  • Topological Polar Surface Area: 35.2
  • XLogP3: 2.5

2,4-Dichloro-6-methoxyaniline Pricemore >>

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2,4-Dichloro-6-methoxyaniline Production Method

Production Method 1

Reaction Conditions
Reference
Preparation of phenylpyrrole derivatives as medical and industrial fungicides and bactericides
, Japan, , ,

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium dithionite Solvents: Ethanol ,  Water ;  14 h, heated
Reference
Synthesis of sterically hindered polychlorinated biphenyl derivatives
Joshi, S. N.; Vyas, S. M.; Duffel, M. W.; Parkin, S.; Lehmler, H.-J., Synthesis, 2011, (7), 1045-1054

Production Method 3

Reaction Conditions
Reference
Preparation of benzoxazole, benzimidazole, and benzothiazole compounds inhibiting production of cytokine in type-2 helper T cell
, Japan, , ,

Production Method 4

Reaction Conditions
Reference
Synthesis and antibacterial activities of less chlorinated analogs of neopyrrolomycin
Tatsuta, Kuniaki; Itoh, Manabu, Journal of Antibiotics, 1994, 47(5), 602-5

2,4-Dichloro-6-methoxyaniline Raw materials

2,4-Dichloro-6-methoxyaniline Preparation Products

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