• 1. Synthesis and use of a new alkene-functionalized SG1-based alkoxyamine
  Claire Bernhardt,Fran?ois Stoffelbach,Bernadette Charleux Polym. Chem. 2011 2 229
• 2. High relaxivity MRI imaging reagents from bimodal star polymers
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• 3. Tunable plasmonic surfaces via colloid assembly
  T. Honold,K. Volk,A. Rauh,J. P. S. Fitzgerald,M. Karg J. Mater. Chem. C 2015 3 11449
• 4. Concise synthesis of (?)-steviamine and analogues and their glycosidase inhibitory activities
  Nadechanok Jiangseubchatveera,Marc E. Bouillon,Boonsom Liawruangrath,Saisunee Liawruangrath,Robert J. Nash,Stephen G. Pyne Org. Biomol. Chem. 2013 11 3826
• 5. Stimuli-responsive microgels for controlled deposition of gold nanoparticles on surfaces
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Quaternary ammonium salts
• Catalysts and Inorganic Chemicals Inorganic Compounds Salt

Introduction to 3-Butenylamine Hydrochloride (CAS No: 17875-18-2)

3-Butenylamine hydrochloride, also known by its CAS number 17875-18-2, is a compound that has garnered significant attention in the fields of organic chemistry and pharmacology due to its unique properties and potential applications. This compound, which exists as the hydrochloride salt of 3-butenylamine, is characterized by its structure, which includes a primary amine group attached to a four-carbon chain with a double bond at the 3-position.

The molecular formula of 3-butenvlamine hydrochloride is C4H9N·HCl, and it has a molecular weight of approximately 96.6 g/mol for the free base and 140.5 g/mol for the hydrochloride salt. Its physical properties include a melting point of around 160°C and a boiling point of approximately 95°C under standard conditions. The compound is typically found in its crystalline form and is soluble in water and various organic solvents such as ethanol and methanol.

Recent studies have highlighted the potential of 3-butenvlamine hydrochloride as a precursor in the synthesis of bioactive molecules, particularly in the development of novel drugs targeting various therapeutic areas such as cancer, inflammation, and neurodegenerative diseases. Researchers have explored its role in forming conjugated systems that exhibit antioxidant and anti-inflammatory properties, making it a valuable intermediate in drug discovery processes.

In terms of synthesis, 3-butenvlamine hydrochloride can be prepared through several methods, including the alkylation of ammonia or primary amines with allyl halides or through the reduction of imines derived from corresponding aldehydes or ketones. The choice of synthetic pathway depends on the availability of starting materials and the desired purity of the final product.

The application of 3-butenvlamine hydrochloride extends beyond pharmaceuticals; it has also been investigated for its role in agrochemicals, where it serves as an intermediate in the synthesis of plant growth regulators and pesticides. Its ability to form stable complexes with metal ions has further expanded its utility in catalytic processes and materials science.

From an environmental standpoint, studies have been conducted to assess the biodegradability and toxicity profile of 3-butenvlamine hydrochloride. These studies are crucial for understanding its potential impact on ecosystems if released into the environment during industrial processes or waste management.

In conclusion, 3-butenvlamine hydrochloride, with its CAS number 17875-18-2, stands out as a versatile compound with diverse applications across multiple scientific disciplines. Ongoing research continues to uncover new avenues for its use, underscoring its importance as both a chemical building block and a potential therapeutic agent.

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