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CAS

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317319-36-1

2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-ylmethanol is a chemical compound belonging to the class of thiazole derivatives. It features a thiazole ring with a fluorinated benzene ring and a methyl group, and the presence of fluorine and trifluoromethyl groups in the benzene ring enhances its potential utility in medicinal chemistry. The hydroxyl group attached to the thiazole ring allows it to act as a hydrogen bond donor or acceptor, making it a promising candidate for drug development.

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  • (2-(2-fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methanol

    Cas No: 317319-36-1

  • USD $ 1.9-2.9 / Gram

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  • 317319-36-1 Structure

  • Basic information

    1. Product Name: {2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol
    2. Synonyms:
    3. CAS NO:317319-36-1
    4. Molecular Formula: C12H9F4NOS
    5. Molecular Weight: 291.2646
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 317319-36-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 374.3°C at 760 mmHg
    3. Flash Point: 180.2°C
    4. Appearance: N/A
    5. Density: 1.419g/cm3
    6. Vapor Pressure: 2.88E-06mmHg at 25°C
    7. Refractive Index: 1.531
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: {2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: {2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol(317319-36-1)
    12. EPA Substance Registry System: {2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol(317319-36-1)

  • 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: 317319-36-1(Hazardous Substances Data)

317319-36-1 Usage

Uses

Used in Pharmaceutical Industry:
2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-ylmethanol is used as a building block for the synthesis of various drugs due to its unique structural features and potential to modulate the biological activity of molecules. Its ability to form hydrogen bonds with target proteins makes it a valuable component in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 317319-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,1 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 317319-36:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*9)+(2*3)+(1*6)=131
131 % 10 = 1
So 317319-36-1 is a valid CAS Registry Number.

317319-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl]methanol

1.2 Other means of identification

Product number -
Other names I14-9262

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:317319-36-1 SDS

317319-36-1Relevant articles and documents

Process development for sodelglitazar: A ppar panagonist

Brown, Andrew D.,Davis, Roman D.,Fitzgerald, Russ N.,Glover, Bobby N.,Harvey, Kim A.,Jones, Lynda A.,Liu, Bing,Patterson, Daniel E.,Sharp, Matthew J.

experimental part, p. 297 - 302 (2010/04/22)

Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier syntheses. This process produces sodelglitazar in 74% overall yield from readily available thiophenol (8) and thiazole alcohol (3).

PROCESS FOR PREPARATION OF CHEMICAL COMPOUNDS

-

Page/Page column 36, (2010/02/07)

The present invention relates to a process for the preparation of certain chemical compounds. In particular, the present invention relates to a method for the preparation of compounds that have been shown to activate human peroxisome proliferator activate

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