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2-amino-1-(3,4-difluorophenyl)ethanol is a chemical compound characterized by the molecular formula C8H10F2NO. It is an amino alcohol featuring a fluorinated phenyl group, which contributes to its unique properties and reactivity. This versatile molecule is a key intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical, agrochemical, and specialty chemical industries.

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  • 10145-04-7 Structure
  • Basic information

    1. Product Name: 2-amino-1-(3,4-difluorophenyl)ethanol
    2. Synonyms: 2-amino-1-(3,4-difluorophenyl)ethanol;AKOS BBV-003391;2-AMino-1-(3,4-difluorophenyl)ethanol HCl
    3. CAS NO:10145-04-7
    4. Molecular Formula: C8H9F2NO
    5. Molecular Weight: 173.161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10145-04-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-amino-1-(3,4-difluorophenyl)ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-1-(3,4-difluorophenyl)ethanol(10145-04-7)
    11. EPA Substance Registry System: 2-amino-1-(3,4-difluorophenyl)ethanol(10145-04-7)
  • Safety Data

    1. Hazard Codes: N/A
    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: 10145-04-7(Hazardous Substances Data)

10145-04-7 Usage

Uses

Used in Pharmaceutical Industry:
2-amino-1-(3,4-difluorophenyl)ethanol serves as a crucial intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications. The presence of the fluorinated phenyl group enhances the compound's lipophilicity, potentially improving drug absorption and distribution in the body.
Used in Agrochemical Industry:
In the agrochemical sector, 2-amino-1-(3,4-difluorophenyl)ethanol is utilized as a building block for the creation of novel agrochemicals. Its incorporation into the molecular structure of these compounds can lead to the development of more effective and targeted pesticides, herbicides, and other agricultural chemicals.
Used in Specialty Chemicals Industry:
2-amino-1-(3,4-difluorophenyl)ethanol also finds application in the production of specialty chemicals. Its unique properties make it suitable for use in the synthesis of various high-value compounds, such as fragrances, dyes, and other specialty chemicals that require specific functional groups and structural features.
Overall, 2-amino-1-(3,4-difluorophenyl)ethanol is a significant molecule in the field of organic chemistry, with its properties and reactivity being extensively studied. Its wide range of applications across different industries highlights its importance and potential for further development and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 10145-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10145-04:
(7*1)+(6*0)+(5*1)+(4*4)+(3*5)+(2*0)+(1*4)=47
47 % 10 = 7
So 10145-04-7 is a valid CAS Registry Number.
InChI:InChI=1S/C8H9F2NO/c9-6-2-1-5(3-7(6)10)8(12)4-11/h1-3,8,12H,4,11H2

10145-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-1-(3,4-difluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names -

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:10145-04-7 SDS

10145-04-7Relevant articles and documents

ARYL-HYDROXYETHYLAMINO-PYRIMIDINES AND TRIAZINES AS MODULATORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 96, (2009/10/18)

Certain aryl-hydroxyethylamino-pyrimidine and triazine compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, energy metabolism disorders, and movement disorders (e.g., multiple sclerosis). Methods of synthesizing such compounds are also disclosed.

SUBSTITUTED IMIDAZOLES AS BOMBESIN RECEPTOR SUBTYPE-3 MODULATORS

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Page/Page column 119, (2008/12/05)

Certain novel substituted imidazoles are ligands of the human bombesin receptor and, in particular, are selective ligands of the human bombesin receptor subtype-3 (BRS-3). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of BRS-3, such as obesity, and diabetes.

Oxazolidinones as alpha 1A receptor antagonists

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, (2008/06/13)

This invention is directed to oxazolidinone compounds which are selective antagonists for human alpha 1A receptors. This invention is also related to uses of these compounds for lowering intraocular pressure, inhibiting cholesterol synthesis, relaxing lower urinary tract tissue, the treatment of benign prostatic hyperplasia, impotency, cardiac arrhythmia and for the treatment of any disease where the antagonism of the alpha 1A receptor may be useful. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.

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