6291-06-1

Usage

Uses

Used in Organic Synthesis:
Cyclobutylammonium chloride is utilized as a phase-transfer catalyst for enhancing the efficiency of organic synthesis reactions. Its ability to transfer ions across different phases makes it particularly useful in reactions involving the transfer of hydroxide ions, such as the Williamson ether synthesis and the Hofmann elimination.
Used in Pharmaceutical Synthesis:
As an important reagent in the field of organic chemistry, cyclobutylammonium chloride is employed in the synthesis of pharmaceuticals. Its role as a phase-transfer catalyst aids in the production of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Synthesis:
Cyclobutylammonium chloride also finds application in the synthesis of agrochemicals, where it serves as a phase-transfer catalyst to improve the efficiency of chemical reactions involved in the production of agricultural chemicals.
Used in Supramolecular Chemistry and Materials Science:
Due to its unique structural and chemical properties, cyclobutylammonium chloride has been studied for its potential use in supramolecular chemistry and materials science. This opens up possibilities for the development of new materials and applications based on its interaction with other molecules and compounds.

InChI:InChI=1/C9H11NO2/c11-7-10-9(12)6-8-4-2-1-3-5-8/h1-5,11H,6-7H2,(H,10,12)

Upstream product

• 103-81-1 Benzeneacetamide 
• 50-00-0 formaldehyd 

Downstream Products

• 340255-36-9 Methyl (4-[2-(acetyloxy)ethoxy]-5-methoxy-2-{[(phenylacetyl)amino]methyl}phenyl)acetate 
• 916220-28-5 methyl 4,5-dimethoxy-2-[(phenylacetamino)methyl]phenylacetate 
• 7500-45-0 N-benzylphenylacetamide 
• 24331-94-0 1,4-dihydro-3(2H)-isoquinolinone 
• 412035-63-3 acetoxy-(2-phenyl-acetylamino)-methane 
• 102010-82-2 phenyl-acetic acid-{[(3,4-diethoxy-phenylsulfanyl)-methyl]-amide} 
• 1636-71-1 2-phenyl-N-piperidin-1-ylmethyl-acetamide 

Relevant academic research and scientific papers

Genetic Encoding and Enzymatic Deprotection of a Latent Thiol Side Chain to Enable New Protein Bioconjugation Applications

The thiol group of the cysteine side chain is arguably the most versatile chemical handle in proteins. To expand the scope of established and commercially available thiol bioconjugation reagents, we genetically encoded a second such functional moiety in f

Light-Emitting Biomarker

The invention concerns novel 1,2-dioxetane derivatives of general formula (I) as defined in the description, capable of emitting a detectable luminescent signal, their use in a method for detecting and/or quantizing a physical, chemical or biological, in particular enzymatic, phenomenon, as well as a kit for implementing said method.

Solvent-free N-hydroxymethylation using formalin over basic alumina

A convenient and high yield method for N-hydroxymethylation of amines with formalin over basic alumina under solvent-free conditions with microwave heating is described.

S-Phenylacetamidomethyl (Phacm): an orthogonal cysteine protecting group for Boc and Fmoc solid-phase peptide synthesis strategies

The reliability of the S-phenylacetamidomethyl-L-cysteine Cys(Phacm), a versatile derivative compatible with both Boc and Fmoc protection schemes, has been examined for solid-phase peptide synthesis.The Phacm group has the same properties as acetamidometh