Cas no 83710-61-6 (1-Bromo-7-methoxynaphthalene)

1-Bromo-7-methoxynaphthalene is a brominated naphthalene derivative featuring a methoxy substituent at the 7-position. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials. The bromine atom at the 1-position offers reactivity for cross-coupling reactions, such as Suzuki or Heck couplings, while the methoxy group enhances solubility and influences electronic properties. Its well-defined structure and stability make it suitable for controlled functionalization in complex molecular frameworks. The compound is typically supplied with high purity, ensuring reliable performance in research and industrial applications. Proper handling and storage are recommended due to its halogenated nature.
1-Bromo-7-methoxynaphthalene structure
1-Bromo-7-methoxynaphthalene structure
Product Name:1-Bromo-7-methoxynaphthalene
CAS No:83710-61-6
MF:C11H9BrO
MW:237.092562437057
MDL:MFCD07435364
CID:1816505
PubChem ID:13025836
Update Time:2025-06-08

1-Bromo-7-methoxynaphthalene Chemical and Physical Properties

Names and Identifiers

    • Naphthalene, 1-bromo-7-methoxy-
    • 1-bromo-7-methoxyNaphthalene
    • 1-bromo-7-methoxy-naphthalene
    • AKOS005264963
    • SCHEMBL5781073
    • CS-13275
    • N14593
    • 6-methoxy-4-bromonaphthalene
    • A19219
    • Glyoxalbis(N-methyl-N-phenylhydrazone)
    • CS-0138977
    • DTXSID701309440
    • 83710-61-6
    • FT-0709162
    • COLPPPMPHPHUPC-UHFFFAOYSA-N
    • 1-Bromo-7-methoxynaphthalene (ACI)
    • DB-075960
    • 1-Bromo-7-methoxynaphthalene
    • MDL： MFCD07435364
    • Inchi： 1S/C11H9BrO/c1-13-9-6-5-8-3-2-4-11(12)10(8)7-9/h2-7H,1H3
    • InChI Key： COLPPPMPHPHUPC-UHFFFAOYSA-N
    • SMILES： BrC1C2C(=CC=C(C=2)OC)C=CC=1

Computed Properties

  • Exact Mass: 235.98368g/mol
  • Monoisotopic Mass: 235.98368g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 172
  • 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
  • Topological Polar Surface Area: 9.2?2

Experimental Properties

  • Density: 1.447±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 68-69 oC
  • Solubility: Almost insoluble (0.036 g/l) (25 o C),

1-Bromo-7-methoxynaphthalene Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Chemenu
CM234169-1000g
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
1000g
 $28320 2021-08-04
TRC
B179385-500mg
1-Bromo-7-methoxynaphthalene
 83710-61-6
500mg
 $ 585.00 2022-06-07
TRC
B179385-1000mg
1-Bromo-7-methoxynaphthalene
 83710-61-6
1g
 $ 970.00 2022-06-07
TRC
B179385-2500mg
1-Bromo-7-methoxynaphthalene
 83710-61-6
2500mg
 $ 1935.00 2022-06-07
Chemenu
CM234169-1000g
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
1000g
 $28320 2022-08-31
Chemenu
CM234169-100mg
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
100mg
 $*** 2023-05-29
Chemenu
CM234169-250mg
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
250mg
 $*** 2023-05-29
Chemenu
CM234169-1g
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
1g
 $*** 2023-05-29
eNovation Chemicals LLC
Y1106046-5g
1-bromo-7-methoxynaphthalene
 83710-61-6 95%
5g
 $1100 2024-07-23
eNovation Chemicals LLC
D517523-1g
1-Bromo-7-methoxynaphthalene
 83710-61-6 95%
1g
 $460 2024-06-05

1-Bromo-7-methoxynaphthalene Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  24 h, rt
Reference
Computationally driven discovery of phenyl(piperazin-1-yl)methanone derivatives as reversible monoacylglycerol lipase (MAGL) inhibitors
Poli, Giulio; et al, Journal of Enzyme Inhibition and Medicinal Chemistry, 2019, 34(1), 589-596

Production Method 2

Reaction Conditions
1.1 Reagents: Iron Solvents: Ethanol ;  2 h, rt
Reference
A Visible Light and Iron-mediated Carbocationic Route to Polysubstituted 1-Halonaphthalenes by Benzannulation using Allylbenzenes and Polyhalomethanes
Roslan, Irwan Iskandar; et al, Advanced Synthesis & Catalysis, 2021, 363(4), 1007-1013

Production Method 3

Reaction Conditions
1.1 Reagents: Sodium nitrite ,  Copper bromide (CuBr) ,  Hydrogen bromide Solvents: Acetonitrile ;  rt; overnight, rt
2.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  24 h, rt
Reference
Computationally driven discovery of phenyl(piperazin-1-yl)methanone derivatives as reversible monoacylglycerol lipase (MAGL) inhibitors
Poli, Giulio; et al, Journal of Enzyme Inhibition and Medicinal Chemistry, 2019, 34(1), 589-596

1-Bromo-7-methoxynaphthalene Raw materials

1-Bromo-7-methoxynaphthalene Preparation Products

1-Bromo-7-methoxynaphthalene Related Literature

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