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613240-34-9

3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 613240-34-9 Structure

  • Basic information

    1. Product Name: 3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol
    2. Synonyms: 3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol;3-(4-Methylpyridin-2-yl)benzyl alcohol;3-(5-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol;3-(5-Hydroxypyridin-2-yl)benzyl alcohol;3-(5-Methylpyridin-2-yl)benzyl alcohol;3-(6-Methylpyridin-2-yl)benzyl alcohol
    3. CAS NO:613240-34-9
    4. Molecular Formula: C13H10F3NO
    5. Molecular Weight: 253.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 613240-34-9.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: 3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol(613240-34-9)
    11. EPA Substance Registry System: 3-(3-(Trifluoromethyl)pyridin-2-yl)benzyl alcohol(613240-34-9)

  • 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: 613240-34-9(Hazardous Substances Data)

613240-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 613240-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,3,2,4 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 613240-34:
(8*6)+(7*1)+(6*3)+(5*2)+(4*4)+(3*0)+(2*3)+(1*4)=109
109 % 10 = 9
So 613240-34-9 is a valid CAS Registry Number.

613240-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[3-(trifluoromethyl)pyridin-2-yl]phenyl]methanol

1.2 Other means of identification

Product number -
Other names 3-(3-(TRIFLUOROMETHYL)(PYRIDIN-2-YL))BENZYL ALCOHOL

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:613240-34-9 SDS

613240-34-9Downstream Products

613240-34-9Relevant articles and documents

IMIDAZOTHIADIAZOLE AND IMIDAZOPYRIDAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION

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Paragraph 00132; 00134, (2013/11/18)

The present invention provides imidazothiadiazole compounds of Formula (I); Wherein W,Y, R0, R2, R4, Ra, Rb, X1, X2, X3 and X4 are as defined herein,, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.

Compounds that modulate PPAR activity and methods for their preparation

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Page 54 - 55, (2010/02/05)

This invention discloses compounds that alter PPAR activity. The invention also discloses pharmaceutically acceptable salts of the compounds, pharmaceutically acceptable compositions comprising the compounds or their salts, and methods of using them as therapeutic agents for treating or preventing disipidemia, hypercholesteremia, obesity, eating disorders, hyperglycemia, atherosclerosis, hypertriglyceridemia, hyperinsulinemia and diabetes in a mammal as well as methods of supressing appetite and modulating leptin levels in a mammal. The present invention also discloses methods for making the disclosed compounds.

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