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3-Fluorophenacylamine hydrochloride is a chemical compound characterized by a central amine group attached to a phenyl ring, featuring an additional fluorine atom and existing in the form of a hydrochloride salt. 3-Fluorophenacylamine hydrochloride is distinguished by its fluorinated structure, which endows it with unique properties and reactivity, and the hydrochloride salt form enhances its solubility and stability, making it a versatile and valuable tool in the pharmaceutical and chemical industries.

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  • 93102-97-7 Structure
  • Basic information

    1. Product Name: 3-Fluorophenacylamine hydrochloride
    2. Synonyms: 3-Fluorophenacylaminehydrochloride95%;2-Amino-3'-fluoroacetophenone hydrochloride, 2-Amino-1-(3-fluorophenyl)ethan-1-one hydrochloride;2-aMino-1-(3-fluorophenyl)ethan-1-one hydrochloride;2-AMino-1-(3-fluorophenyl)ethanone hydrochloride;2-Amino-1-(3-fluorophenyl)ethanone HCl
    3. CAS NO:93102-97-7
    4. Molecular Formula: C8H8FNO*ClH
    5. Molecular Weight: 189.61
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93102-97-7.mol
  • Chemical Properties

    1. Melting Point: 201-204
    2. Boiling Point: 290.4°Cat760mmHg
    3. Flash Point: 129.4°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 0.00157mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Fluorophenacylamine hydrochloride(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Fluorophenacylamine hydrochloride(93102-97-7)
    12. EPA Substance Registry System: 3-Fluorophenacylamine hydrochloride(93102-97-7)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93102-97-7(Hazardous Substances Data)

93102-97-7 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Fluorophenacylamine hydrochloride is used as a precursor in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and reactivity make it a key component in the development of new drugs with potential therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-Fluorophenacylamine hydrochloride is utilized as a building block for creating novel substances. Its fluorinated structure allows for the exploration of new chemical pathways and the enhancement of existing compounds, contributing to drug discovery and the advancement of medical treatments.
Used in Chemical Industry:
3-Fluorophenacylamine hydrochloride is also employed in the chemical industry for its enhanced solubility and stability. These properties make it suitable for a range of applications, including the development of new materials and the improvement of existing chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 93102-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93102-97:
(7*9)+(6*3)+(5*1)+(4*0)+(3*2)+(2*9)+(1*7)=117
117 % 10 = 7
So 93102-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8FNO.ClH/c9-7-3-1-2-6(4-7)8(11)5-10;/h1-4H,5,10H2;1H

93102-97-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(3-fluorophenyl)ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Fluorophenacylamine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:93102-97-7 SDS

93102-97-7Relevant articles and documents

New 1,3-oxazolo[4,5-c]quinoline derivatives: Synthesis and evaluation of antibacterial and antituberculosis properties

Eswaran, Sumesh,Adhikari, Airody Vasudeva,Ajay Kumar

experimental part, p. 957 - 966 (2010/04/26)

A new class of fused oxazoloquinoline derivatives was synthesized starting from 2-bromo-1-phenylethanones 1a-b through multi-step reactions. The newly synthesized compounds were evaluated for their in vitro antibacterial against Escherichia coli (ATTC-259

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