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1111110-54-3

2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine is a pyridine derivative with the molecular formula C12H8F3NO. It features a hydroxy group and a trifluoromethylphenyl group attached to the 2 and 6 positions of the pyridine ring, respectively. 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in medicinal chemistry and drug discovery due to its unique structural features and biological activities.

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  • 1111110-54-3 Structure

  • Basic information

    1. Product Name: 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine
    2. Synonyms: 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine;6-(4-(TrifluoroMethyl)phenyl)pyridin-2-ol
    3. CAS NO:1111110-54-3
    4. Molecular Formula: C12H8F3NO
    5. Molecular Weight: 239.1932296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1111110-54-3.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: 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine(1111110-54-3)
    11. EPA Substance Registry System: 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine(1111110-54-3)

  • 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: 1111110-54-3(Hazardous Substances Data)

1111110-54-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structural features and reactivity make it a valuable component in the development of new drugs and pesticides.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine is utilized for its potential biological activities. Its structural properties allow it to be a promising candidate for the development of new therapeutic agents and pharmaceutical compounds.
Used in Chemical and Industrial Processes:
Due to its unique properties and reactivity, 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine may also be employed in various chemical and industrial processes. Its versatility and potential applications make it a valuable compound for research and development in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1111110-54-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,1,1 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1111110-54:
(9*1)+(8*1)+(7*1)+(6*1)+(5*1)+(4*1)+(3*0)+(2*5)+(1*4)=53
53 % 10 = 3
So 1111110-54-3 is a valid CAS Registry Number.

1111110-54-3SDS

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 6-(4-(Trifluoromethyl)phenyl)pyridin-2-ol

1.2 Other means of identification

Product number -
Other names 6-[4-(trifluoromethyl)phenyl]-1H-pyridin-2-one

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:1111110-54-3 SDS

1111110-54-3Relevant articles and documents

Vinylogous Blaise Reaction: Conceptually New Synthesis of Pyridin-2-ones

Rao, H. Surya Prakash,Muthanna, Nandurka,Padder, Ashiq Hussain

supporting information, p. 1649 - 1653 (2018/06/26)

A conceptually new synthesis of pyridine rings by a [C 4 + CN] assembly has been developed by applying a vinylogous version of the classic Blaise reaction. The zinc-mediated reaction of (het)aryl or alkyl nitriles with ethyl-4-bromocrotonate pr

Synthesis of mono- and diaza-'pyridones' via stille coupling of alkoxystannanes

Smith, Charlotte L.,Hirschh?user, Christoph,Malcolm, Georgia K.,Nasrallah, Daniel J.,Gallagher, Timothy

, p. 1904 - 1908 (2014/08/18)

Various alkoxy-substituted heterocyclic stannanes provide access to the corresponding substituted 'pyridone' moieties via Stille cross-coupling. Both pyridyl and a series of diazinyl stannanes are prepared, and options for unmasking (via demethylation or debenzylation) of the pyridone unit are evaluated. Georg Thieme Verlag Stuttgart. New York.

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