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[4-(2,2,2-Trifluoro-ethoxy)-pyridin-2-yl]-methanol, also known as TFPM, is a chemical compound characterized by its molecular formula C9H8F3NO2. It is a white solid with a molecular weight of 217.16 g/mol. TFPM is recognized for its versatility in organic synthesis and pharmaceutical research, where it serves as a building block and a ligand for metal catalysts. Its utility extends to the preparation of various organic compounds, the development of new materials, and the production of fine chemicals. Due to its potential to cause irritation, it is crucial to handle TFPM with appropriate safety measures.

103577-65-7

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103577-65-7 Usage

Uses

Used in Organic Synthesis:
TFPM is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic compounds, enhancing the diversity and functionality of synthesized products.
Used in Pharmaceutical Research:
In pharmaceutical research, TFPM is utilized as a ligand for metal catalysts, which is instrumental in facilitating various chemical reactions essential for the development of new pharmaceuticals.
Used in the Development of New Materials:
TFPM is employed in the development of new materials due to its unique properties that can be integrated into the design and synthesis of advanced materials with specific applications.
Used in the Production of Fine Chemicals:
TFPM is used in the production of fine chemicals, where its reactivity and structural features are leveraged to create high-quality specialty chemicals for various industries.
Used in Chemical Compound Preparation:
TFPM is used as a reagent in the preparation of various organic compounds, contributing to the synthesis of molecules with potential applications in different fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 103577-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,7 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103577-65:
(8*1)+(7*0)+(6*3)+(5*5)+(4*7)+(3*7)+(2*6)+(1*5)=117
117 % 10 = 7
So 103577-65-7 is a valid CAS Registry Number.

103577-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methanol

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:103577-65-7 SDS

103577-65-7Downstream Products

103577-65-7Relevant articles and documents

ANALOGS OF 2-PRALIDOXIME AS ANTIDOTES AGAINST ORGANOPHOSPHORUS NERVE AGENTS

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Paragraph 00101, (2020/02/23)

Provided herein are compounds useful in treating exposure to an organophosphorus compound, such as a nerve agent, pesticide, or, generally, an acetylcholinesterase inhibitor, such as sarin. Compositions, e.g. pharmaceutical compositions or dosage forms, comprising the compounds also are provided herein. Methods of treating a patient exposed to a nerve agent, pesticide, or, generally, an acetylcholinesterase inhibitor, e.g., an organophosphorus compound, such as sarin, also are provided.

2--1H-thienoimidazoles. A Novel Class of Gastric H+/K+-ATPase Inhibitors

Weidmann, Klaus,Herling, Andreas W.,Lang, Hans-Jochen,Scheunemann, Karl-Heinz,Rippel, Robert,et al.

, p. 438 - 450 (2007/10/02)

2-thienoimidazoles were synthesized and investigated as potential inhibitors of gastric H+/K+-ATPase.The isomers of the two possible thienoimidazole series were found to be potent inhibitors of gastric acid secretion in vitro and in vivo.Structure-activity relationships indicate that especially lipophilic alkoxy, benzyloxy, and phenoxy substituents with additional electron-demanding properties in the 4-position of the pyridine moiety combined with an unsubstituted thienoimidazole lead to highly active compounds with a favorable chemical stability.Various substitution patterns in the thienoimidazole moiety result in lower biological activity.The heptafluorobutyloxy derivative saviprazole (HOE 731, 5d) was selected for further development and is currently undergoing clinical evaluation.Comprehensive pharmacological studies indicate a pharmacodynamic profile different to omeprazole, the first H+/K+-ATPase blocker introduced on the market.

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