1408057-44-2 Usage
Description
[(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol is a chiral organic compound with the molecular formula C6H10F2NO. It features a pyrrolidine ring, which is a five-membered nitrogen-containing ring, with a hydroxymethyl group and a methyl group attached to the nitrogen atom. [(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol is characterized by its stereochemistry, with the "2S" configuration indicating the specific arrangement of atoms in the molecule. The presence of two fluorine atoms on the carbon atoms of the pyrrolidine ring further distinguishes this compound, which is known for its potential applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Synthesis:
[(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structural features, including the fluorinated pyrrolidine ring and the chiral center, make it a valuable building block in medicinal chemistry.
Used in Fine Chemicals Production:
[(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol is also utilized in the production of fine chemicals, where its specific stereochemistry and fluorinated groups can impart unique properties to the final products, enhancing their performance in various applications.
Used in Chiral Non-racemic Catalyst Preparation:
[(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol is used as a precursor in the preparation of chiral non-racemic catalysts. The chiral nature of the compound allows for the creation of catalysts that can selectively promote certain reactions, which is crucial in asymmetric synthesis and the production of enantiomerically pure compounds.
Used in Biological Research and Drug Discovery:
Due to its stereochemical arrangement and fluorinated groups, [(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]methanol may possess potential biological properties and pharmacological activities. It can be used in biological research to explore its interactions with biological targets and in drug discovery for the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1408057-44-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,0,5 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1408057-44:
(9*1)+(8*4)+(7*0)+(6*8)+(5*0)+(4*5)+(3*7)+(2*4)+(1*4)=142
142 % 10 = 2
So 1408057-44-2 is a valid CAS Registry Number.
1408057-44-2Relevant articles and documents
Kras-G12C inhibitor heterocyclic compounds
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Paragraph 0539; 0546-0549, (2021/06/23)
The invention relates to Kras-G12C inhibitor heterocyclic compounds represented by formula I, a preparation method thereof, and application of the Kras-G12C inhibitor heterocyclic compounds in prevention and treatment of tumor diseases such as lung cancer, colorectal cancer and pancreatic cancer. In the preparation process, the compounds of the general formula I are obtained through a series of reactions such as SN2 reaction, protection, coupling reaction, deprotection, condensation reaction and the like.
NOVEL INDOLE DERIVATIVES AND THEIR USE IN NEURODEGENERATIVE DISEASES
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Paragraph 0873-0874, (2016/11/24)
The present invention relates to indole compounds, and pharmaceutically acceptable compositions thereof, useful as antagonists of P2X7, and for the treatment of P2X7-related disorders.
