Cas no 863870-87-5 (3-Bromo-2-chlorophenol)

3-Bromo-2-chlorophenol structure
3-Bromo-2-chlorophenol structure
Product Name:3-Bromo-2-chlorophenol
CAS No:863870-87-5
MF:C6H4BrClO
MW:207.452360153198
MDL:MFCD08166321
CID:720336
PubChem ID:6455237
Update Time:2024-10-26

3-Bromo-2-chlorophenol Chemical and Physical Properties

Names and Identifiers

    • 3-Bromo-2-chlorophenol
    • Phenol, 3-bromo-2-chloro-
    • 3-AMINO 4 ETHOXY ACETANILIDE
    • Phenol, bromochloro-
    • bromochlorophenol
    • Phenol,3-bromo-2-chloro-
    • PubChem16946
    • 2-Chloro-3-bromophenol
    • KSC493Q4L
    • DUKKNDLIWRYBCT-UHFFFAOYSA-N
    • CL8469
    • STL554946
    • BBL101150
    • AS06539
    • VZ26404
    • LS10087
    • CM10471
    • BC004178
    • SY027065
    • ST2410504
    • AB0034236
    • AM20050176
    • 3-Bromo-2-chlorophenol (ACI)
    • MDL： MFCD08166321
    • Inchi： 1S/C6H4BrClO/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
    • InChI Key： DUKKNDLIWRYBCT-UHFFFAOYSA-N
    • SMILES： ClC1C(O)=CC=CC=1Br

Computed Properties

  • Exact Mass: 205.91300
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 99.1
  • XLogP3: 2.9
  • Topological Polar Surface Area: 20.2

Experimental Properties

  • Boiling Point: 246.1℃ at 760 mmHg
  • PSA: 20.23000
  • LogP: 2.80810

3-Bromo-2-chlorophenol Customs Data

  • HS CODE：2908199090
  • Customs Data：

    China Customs Code:

    2908199090

    Overview:

    HS:2908199090 Derivatives of other phenols and phenolic alcohols containing only halogen substituents and their salts 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: 2908199090. derivatives of polyphenols or phenol-alcohols containing only halogen substituents and their salts. VAT:17.0%. tax rebate rate:9.0%. supervision conditions:None. MFN tariff:5.5%. general tariff:30.0%

3-Bromo-2-chlorophenol Pricemore >>

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3-Bromo-2-chlorophenol Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  overnight, reflux
Reference
Design, synthesis, and evaluation of GLUT inhibitors
Granchi, Carlotta; et al, Methods in Molecular Biology (New York, 2018, 1713, 93-108

Production Method 2

Reaction Conditions
1.1 Reagents: Chlorosuccinimide Catalysts: N,N′′-(1R,2R)-1,2-Cyclohexanediylbis[N′-[3,5-bis(trifluoromethyl)phenyl]thiourea Solvents: Chloroform-d ;  3 h, rt
Reference
The Catalyst-Controlled Regiodivergent Chlorination of Phenols
Maddox, Sean M.; et al, Organic Letters, 2016, 18(21), 5476-5479

Production Method 3

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  6.5 h, reflux
1.2 Reagents: Hydrochloric acid Solvents: Water ;  neutralized, rt
Reference
A New and Efficient Synthesis of 4-Functionalized Benzo[b]furans from 2,3-Dihalophenols
Sanz, Roberto; et al, Journal of Organic Chemistry, 2005, 70(16), 6548-6551

Production Method 4

Reaction Conditions
1.1 Reagents: Diisopropylamine ,  Butyllithium Solvents: Tetrahydrofuran ,  Hexane ;  30 min, 0 °C; 0 °C → -78 °C
1.2 30 min, -78 °C
1.3 30 min, -78 °C; -78 °C → rt
2.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  6.5 h, reflux
2.2 Reagents: Hydrochloric acid Solvents: Water ;  neutralized, rt
Reference
A New and Efficient Synthesis of 4-Functionalized Benzo[b]furans from 2,3-Dihalophenols
Sanz, Roberto; et al, Journal of Organic Chemistry, 2005, 70(16), 6548-6551

Production Method 5

Reaction Conditions
1.1 Reagents: Diisopropylamine ,  Butyllithium Solvents: Tetrahydrofuran ;  0 °C → -78 °C; 1 h, -78 °C
1.2 Reagents: Hexachloroethane Solvents: Tetrahydrofuran ;  30 min, -78 °C
2.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  overnight, reflux
Reference
Design, synthesis, and evaluation of GLUT inhibitors
Granchi, Carlotta; et al, Methods in Molecular Biology (New York, 2018, 1713, 93-108

Production Method 6

Reaction Conditions
1.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  3 h, rt
2.1 Reagents: Diisopropylamine ,  Butyllithium Solvents: Tetrahydrofuran ;  0 °C → -78 °C; 1 h, -78 °C
2.2 Reagents: Hexachloroethane Solvents: Tetrahydrofuran ;  30 min, -78 °C
3.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  overnight, reflux
Reference
Design, synthesis, and evaluation of GLUT inhibitors
Granchi, Carlotta; et al, Methods in Molecular Biology (New York, 2018, 1713, 93-108

Production Method 7

Reaction Conditions
1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran ,  Hexane ;  10 min, -78 °C; -78 °C → rt; 30 min, rt
1.2 Solvents: Tetrahydrofuran ;  36 h, reflux
2.1 Reagents: Diisopropylamine ,  Butyllithium Solvents: Tetrahydrofuran ,  Hexane ;  30 min, 0 °C; 0 °C → -78 °C
2.2 30 min, -78 °C
2.3 30 min, -78 °C; -78 °C → rt
3.1 Reagents: Sodium hydroxide Solvents: Ethanol ;  6.5 h, reflux
3.2 Reagents: Hydrochloric acid Solvents: Water ;  neutralized, rt
Reference
A New and Efficient Synthesis of 4-Functionalized Benzo[b]furans from 2,3-Dihalophenols
Sanz, Roberto; et al, Journal of Organic Chemistry, 2005, 70(16), 6548-6551

Production Method 8

Reaction Conditions
1.1 Reagents: 1,3-Dichloro-5,5-dimethylhydantoin Catalysts: 2-Propanamine, N-(1-methylethyl)-, hydrochloride (1:1) Solvents: Toluene ;  4 h, 0 °C
1.2 Reagents: Sodium sulfite Solvents: Water
Reference
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
Xiong, Xiaodong ; et al, ACS Catalysis, 2018, 8(5), 4033-4043

3-Bromo-2-chlorophenol Raw materials

3-Bromo-2-chlorophenol Preparation Products

3-Bromo-2-chlorophenol Related Literature

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