Cas no 90430-14-1 (4-(Aminomethyl)phenol hydrobromide)

4-(Aminomethyl)phenol hydrobromide structure
90430-14-1 structure
Product Name:4-(Aminomethyl)phenol hydrobromide
CAS No:90430-14-1
MF:C7H10BrNO
MW:204.06440114975
MDL:MFCD00870499
CID:798352
PubChem ID:2759293
Update Time:2025-09-27

4-(Aminomethyl)phenol hydrobromide Chemical and Physical Properties

Names and Identifiers

    • 4-(Aminomethyl)phenol hydrobromide
    • 4-Hydroxybenzylamine hydrobromide
    • Phenol,4-(aminomethyl)-, hydrobromide (1:1)
    • 4-Aminomethyl-phenol,Hydrobromid
    • 4-hydroxy-benzylamine hbr
    • 4-hydroxybenzylammonium bromide
    • Phenol, 4-(aminomethyl)-, hydrobromide (9CI)
    • A10196
    • 4-(Aminomethyl)phenolhydrobromide
    • AS-44225
    • AB11678
    • 4-Hydroxy-benzylamine hydrobromide
    • 4-(Aminomethyl)phenol HBr
    • 4-(aminomethyl)phenol;hydrobromide
    • F2158-0362
    • 4-(Aminomethyl)phenol monohydrobromide
    • p-hydroxybenzylamine-hydrobromide
    • (4-HYDROXYPHENYL)METHANAMINIUM BROMIDE
    • DTXSID50374723
    • DB-078677
    • SCHEMBL3539884
    • MFCD02258769
    • 90430-14-1
    • 4-hydroxybenzylamine hbr
    • p-hydroxybenzylamine.hydrobromide
    • AKOS016000982
    • 4-hydroxybenzylamine hydrobromide 696-60-6
    • 4-aminomethyl-phenol hydrobromide
    • ZJKNRZBDZNVNRX-UHFFFAOYSA-N
    • MDL: MFCD00870499
    • Inchi: 1S/C7H9NO.BrH/c8-5-6-1-3-7(9)4-2-6;/h1-4,9H,5,8H2;1H
    • InChI Key: ZJKNRZBDZNVNRX-UHFFFAOYSA-N
    • SMILES: Br.OC1C=CC(CN)=CC=1

Computed Properties

  • Exact Mass: 202.99500
  • Monoisotopic Mass: 202.995
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 77
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 46.2A^2

Experimental Properties

  • Melting Point: 200-203°C
  • Boiling Point: 262.4°Cat760mmHg
  • Flash Point: 112.5°C
  • PSA: 46.25000
  • LogP: 2.50930

4-(Aminomethyl)phenol hydrobromide Security Information

4-(Aminomethyl)phenol hydrobromide Customs Data

  • HS CODE:2922299090
  • Customs Data:

    China Customs Code:

    2922299090

    Overview:

    2922299090. Other amino groups(naphthol\phenol)And ether\Esters [including their salts, Except those containing more than one oxygen-containing group]. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Summary:

    2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

4-(Aminomethyl)phenol hydrobromide Pricemore >>

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4-(Aminomethyl)phenol hydrobromide Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrogen bromide ;  2 h, reflux
Reference
Metal-Organic Self-Assembled Trefoil Knots for C-Br Bond Activation
Prakasam, Thirumurugan; et al, ACS Catalysis, 2019, 9(3), 1907-1914

Production Method 2

Reaction Conditions
Reference
N-(4-Hydroxybenzyl)-3,4,5-trimethoxybenzamide and its use in the preparation of trimethobenzamide hydrochloride
, France, , ,

Production Method 3

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Water ;  0 °C; 0 °C → rt; rt → reflux
Reference
Biology-oriented synthesis of a natural-product inspired oxepane collection yields a small-molecule activator of the Wnt-pathway
Basu, Sudipta; et al, Proceedings of the National Academy of Sciences of the United States of America, 2011, 108(17), 6805-6810

Production Method 4

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Water ;  6 h, reflux
Reference
Nanoscale Borromeates
Chichak, Kelly S.; et al, Journal of Organic Chemistry, 2005, 70(20), 7956-7962

Production Method 5

Reaction Conditions
Reference
N-(4-Hydroxybenzyl)-3,4,5-trimethoxybenzamide and its use in the preparation of trimethobenzamide hydrochloride
, France, , ,

4-(Aminomethyl)phenol hydrobromide Raw materials

4-(Aminomethyl)phenol hydrobromide Preparation Products

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