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CAS

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438554-18-8

2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 438554-18-8 Structure

  • Basic information

    1. Product Name: 2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE
    2. Synonyms: 2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE
    3. CAS NO:438554-18-8
    4. Molecular Formula: C9H5F3N2
    5. Molecular Weight: 198.1446096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 438554-18-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 332.9±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.426±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 11.92±0.24(Predicted)
    10. CAS DataBase Reference: 2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE(438554-18-8)
    12. EPA Substance Registry System: 2-(2,3,4-TRIFLUORO-PHENYL)-1H-IMIDAZOLE(438554-18-8)

  • 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: 438554-18-8(Hazardous Substances Data)

438554-18-8 Usage

Appearance

White to off-white solid

Molecular weight

215.16 g/mol

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals, manufacturing of rubber accelerators, dyes, and other organic compounds

Importance

Versatile building block in organic chemistry with various applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 438554-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,5,5 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 438554-18:
(8*4)+(7*3)+(6*8)+(5*5)+(4*5)+(3*4)+(2*1)+(1*8)=168
168 % 10 = 8
So 438554-18-8 is a valid CAS Registry Number.

438554-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3,4-trifluorophenyl)-1H-imidazole

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:438554-18-8 SDS

438554-18-8Downstream Products

438554-18-8Relevant articles and documents

Heteroaryl substituted fused bicyclic heteroaryl compound as GABAA receptor ligands

-

, (2008/06/13)

This invention relates to heteroaryl substituted fused bicyclic heteroaryl compounds, such as heteroaryl substituted imidazopyridines, imidazopyrazines, imidazopyridizines, imidazopyrimidines, and imidazothiazoles, which may be described by Formula I or F

Benzimidazole and pyridylimidazole derivatives

-

, (2008/06/13)

This invention relates to benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds, all of which may be described by of Formula I The invention is particularly related to such compounds that bind with high selectivity and high affinity to the benzodiazepine site of GABAA receptors. This invention also relates to pharmaceutical compositions comprising such compounds and to the use of such compounds in treatment of certain central nervous system (CNS) diseases. Novel processes for preparing compounds of Formula I are disclosed. This invention also relates to the use of benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds of Formula I in combination with one or more other CNS agents to potentiate the effects of the other CNS agents. Additionally this invention relates to the use such compounds as probes for the localization of GABAA receptors in tissue sections.

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