262852-00-6

Basic information

• Product Name: Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)- (9CI)
• Synonyms: Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)- (9CI);1-(3-Fluorobicyclo[1.1.1]pentan-1-yl)ethan-1-one
• CAS NO: 262852-00-6
• Molecular Formula: C7H9FO
• Molecular Weight: 128.1441632
• Product Categories: ACETYLGROUP
• Mol File: 262852-00-6.mol

Chemical Properties

• Boiling Point: 147.6±40.0 °C(Predicted)
• Appearance: /
• Density: 1.16±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)- (9CI)(262852-00-6)
• EPA Substance Registry System: Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)- (9CI)(262852-00-6)

Safety Data

• Hazardous Substances Data: 262852-00-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)(9CI) is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure may allow it to interact with biological targets, offering new avenues for drug development and treatment of various diseases.
Used in Agrochemical Industry:
In the agrochemical industry, Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)(9CI) may be utilized as an active ingredient in pesticides or herbicides. Its specific chemical properties could provide novel modes of action, leading to more effective and targeted pest control solutions.
Used in Materials Science:
Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)(9CI) may also find applications in materials science, where its unique structure and properties could be leveraged to develop new materials with specific characteristics. This could include the creation of advanced polymers, coatings, or other materials with improved performance attributes.
Further research is necessary to fully understand the potential uses and effects of Ethanone, 1-(3-fluorobicyclo[1.1.1]pent-1-yl)(9CI) on biological systems, as well as to optimize its synthesis and application in various industries.

Upstream product

• 146038-53-1 3-fluorobicyclo<1.1.1>pentane-1-carboxylic acid 
• 56842-95-6 bicyclo<1.1.1>pentane-1,3-dicarboxylic acid 
• 75-16-1 methylmagnesium bromide 
• 917-54-4 methyllithium 

Relevant articles and documents

Practical and Modular Construction of C(sp3)-Rich Alkyl Boron Compounds

Alkyl boronic acids and esters play an important role in the synthesis of C(sp3)-rich medicines, agrochemicals, and material chemistry. This work describes a new type of transition-metal-free mediated transformation to enable the construction of C(sp3)-rich and sterically hindered alkyl boron reagents in a practical and modular manner. The broad generality and functional group tolerance of this method is extensively examined through a variety of substrates, including synthesis and late-stage functionalization of scaffolds relevant to medicinal chemistry. The strategic significance of this approach, with alkyl boronic acids as linchpins, is demonstrated through various downstream functionalizations of the alkyl boron compounds. This two-step concurrent cross-coupling approach, resembling formal and flexible alkyl-alkyl couplings, provides a general entry to synthetically challenging high Fsp3-containing drug-like scaffolds.

POLYHETEROCYCLIC COMPOUNDS AS METTL3 INHIBITORS

The present invention relates to compounds of formula (I) that function as inhibitors of METTL3 (N6-adenosine-methyltransferase 70 kDa subunit) enzyme activity: X-Y-Z (I) wherein X, Y and Z are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, and autoimmune diseases, as well as other diseases or conditions in which METTL3 activity is implicated.