Cas no 93102-96-6 (2-Amino-1-(2-fluorophenyl)ethanone hydrochloride)

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride is a fluorinated aromatic ketone derivative with significant utility in pharmaceutical and organic synthesis. Its key structural features include a primary amine group and a fluorine-substituted phenyl ring, making it a versatile intermediate for the development of bioactive compounds. The hydrochloride salt form enhances stability and solubility, facilitating handling and reaction efficiency. This compound is particularly valuable in the synthesis of heterocyclic frameworks and pharmacologically active molecules, where the fluorine moiety can influence binding affinity and metabolic stability. Its high purity and well-defined chemical properties ensure reproducibility in research and industrial applications.
2-Amino-1-(2-fluorophenyl)ethanone hydrochloride structure
93102-96-6 structure
Product Name:2-Amino-1-(2-fluorophenyl)ethanone hydrochloride
CAS No:93102-96-6
MF:C8H9ClFNO
MW:189.614564657211
MDL:MFCD08532458
CID:1026205
Update Time:2025-06-07

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-1-(2-fluorophenyl)ethanone hydrochloride
    • 2-FLUOROPHENACYLAMINE HYDROCHLORID
    • 2-Fluorophenacylamine hydrochloride
    • 2-amino-1-(2-fluorophenyl)ethan-1-one hydrochloride
    • 2-AMINO-1-(2-FLUOROPHENYL)ETHANONE HCL
    • 2-Fluorophenacylamine, HCl
    • GFHFMCRPNVXGFL-UHFFFAOYSA-N
    • PC4573
    • SBB091010
    • AX8218930
    • AB0027720
    • ST
    • Ethanone, 2-amino-1-(2-fluorophenyl)-, hydrochloride (9CI)
    • MDL: MFCD08532458
    • Inchi: 1S/C8H8FNO.ClH/c9-7-4-2-1-3-6(7)8(11)5-10;/h1-4H,5,10H2;1H
    • InChI Key: GFHFMCRPNVXGFL-UHFFFAOYSA-N
    • SMILES: Cl.O=C(CN)C1C(F)=CC=CC=1

Computed Properties

  • Exact Mass: 189.03600
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 149
  • Topological Polar Surface Area: 43.1

Experimental Properties

  • PSA: 43.09000
  • LogP: 2.46940

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Customs Data

  • HS CODE:2922399090
  • Customs Data:

    China Customs Code:

    2922399090

    Overview:

    2922399090 Other amino aldehydes\Amino ketones and their salts(Including aminoquinone and its salts,Except those containing more than one oxygen-containing group). VAT:17.0% Tax refund rate:9.0% 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:

    2922399090 other amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd.
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93102-96-6 98%
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Fluorochem
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2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrochloric acid
Reference
Syntheses of 2-mercapto-4-substituted imidazole derivatives with antiinflammatory properties
Maeda, Sadao; Suzuki, Mamoru; Iwasaki, Tameo; Matsumoto, Kazuo; Iwasawa, Yoshio, Chemical & Pharmaceutical Bulletin, 1984, 32(7), 2536-43

Production Method 2

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Chloroform ;  2 h, 50 °C
1.2 Reagents: Hydrochloric acid Solvents: Ethanol ,  Water ;  4 h, reflux
Reference
Combating fluconazole-resistant fungi with novel β-azole-phenylacetone derivatives
Zhao, Liyu; Sun, Nannan; Tian, Linfeng; Sun, Yin; Chen, Yixuan; et al, European Journal of Medicinal Chemistry, 2019, 183,

Production Method 3

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Chloroform
Reference
Anomalous reaction of pentafluorophenacyl bromide with hexamethylenetetramine. Structure of the product
Henry, Ronald A.; Hollins, Richard A.; Lowe-Ma, Charlotte; Moore, Donald W.; Nissan, Robin A., Journal of Organic Chemistry, 1990, 55(6), 1796-801

Production Method 4

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Dichloromethane ;  15 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Ethanol ;  72 h, rt
Reference
An approach to the synthesis of 4-aryl and 5-aryl substituted thiazole-2(3H)-thiones employing flow processing
Balti, Monaem; Miller, Shelli A.; Efrit, Mohamed Lotfi; Leadbeater, Nicholas E., RSC Advances, 2016, 6(76), 72165-72169

Production Method 5

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Chloroform ;  2 h, 50 °C
1.2 Reagents: Hydrochloric acid Solvents: Ethanol ,  Water ;  2 h, rt → reflux
Reference
Double C-S bond formation via multiple Csp3-H bond cleavage: synthesis of 4-hydroxythiazoles from amides and elemental sulfur under metal-free conditions
Chen, Liang; Xuchen, Xinyu; Wang, Fei; Yang, Yuan; Deng, Guobo; et al, Organic & Biomolecular Chemistry, 2021, 19(46), 10068-10072

Production Method 6

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Chloroform ;  50 °C
1.2 Reagents: Hydrochloric acid Solvents: Ethanol ,  Water ;  reflux
Reference
Design, synthesis and evaluation of novel 5-phenylthiophene derivatives as potent fungicidal of Candida albicans and antifungal reagents of fluconazole-resistant fungi
Yin, Wenbo; Zhang, Yuxin; Cui, Hengxian; Jiang, Hong; Liu, Lei; et al, European Journal of Medicinal Chemistry, 2021, 225,

Production Method 7

Reaction Conditions
1.1 Reagents: Hexamethylenetetramine Solvents: Chloroform ;  rt; 15 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Ethanol ,  Water ;  96 h, rt
Reference
New antipsychotic agents with serotonin and dopamine antagonist properties based on a pyrrolo[2,1-b][1,3]benzothiazepine structure
Campiani, Giuseppe; Nacci, Vito; Bechelli, Susanna; Ciani, Silvia M.; Garofalo, Antonio; et al, Journal of Medicinal Chemistry, 1998, 41(20), 3763-3772

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Raw materials

2-Amino-1-(2-fluorophenyl)ethanone hydrochloride Preparation Products

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