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6-(2-Trifluoromethylphenyl)-picolinic acid is a chemical compound that belongs to the class of picolinic acids. It is characterized by the presence of a trifluoromethyl group and a phenyl group attached to the picolinic acid moiety. This unique structure endows it with potential biological activities and makes it a valuable molecule for research and development in the field of chemical and pharmaceutical sciences.

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  • 887983-43-9 Structure
  • Basic information

    1. Product Name: 6-(2-Trifluoromethylphenyl)-picolinic acid
    2. Synonyms: 6-(2-Trifluoromethylphenyl)-picolinic acid;6-(2-Trifluoromethylphenyl)-2-pyridinecarboxylic acid
    3. CAS NO:887983-43-9
    4. Molecular Formula: C13H8F3NO2
    5. Molecular Weight: 267.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887983-43-9.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-(2-Trifluoromethylphenyl)-picolinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(2-Trifluoromethylphenyl)-picolinic acid(887983-43-9)
    11. EPA Substance Registry System: 6-(2-Trifluoromethylphenyl)-picolinic acid(887983-43-9)
  • 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: 887983-43-9(Hazardous Substances Data)

887983-43-9 Usage

Uses

Used in Medicinal Chemistry:
6-(2-Trifluoromethylphenyl)-picolinic acid is used as a building block for the development of pharmaceuticals and agrochemicals. Its unique structure and properties allow it to be incorporated into the synthesis of novel compounds with diverse pharmacological properties.
Used in Pharmaceutical Industry:
6-(2-Trifluoromethylphenyl)-picolinic acid is used as a key intermediate in the synthesis of various drugs. Its potential biological activities make it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Industry:
6-(2-Trifluoromethylphenyl)-picolinic acid is used as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure and properties contribute to the development of more effective and environmentally friendly agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 887983-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,9,8 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 887983-43:
(8*8)+(7*8)+(6*7)+(5*9)+(4*8)+(3*3)+(2*4)+(1*3)=259
259 % 10 = 9
So 887983-43-9 is a valid CAS Registry Number.

887983-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[2-(trifluoromethyl)phenyl]pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-[(2-Trifluoromethyl)phenyl]pyridine-2-carboxylic acid

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:887983-43-9 SDS

887983-43-9Downstream Products

887983-43-9Relevant articles and documents

A chiral picolinic acid ligand, Cl-NAPH-PyCOOH, for CPRU-catalyzed dehydrative allylation: Design, synthesis, and properties

Tanaka, Shinji,Suzuki, Yusuke,Kimura, Takahiro,Kitamura, Masato

, p. 1707 - 1720 (2019)

A CpRu/Br?nsted acid-combined catalyst, CpRu(II)/pico-linic acid (PyCOOH), acts as an efficient catalyst for the allyl protection/deprotection of alcohols. This discovery has resulted in the development of a new axially chiral ligand, Cl-Naph-PyCOOH (2a;

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