• 1. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 2. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
  Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
• 3. Excellent electrochemical performance of LiFe0.4Mn0.6PO4 microspheres produced using a double carbon coating process?
  Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
• 4. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
  Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
• 5. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Comprehensive Guide to 3-Amino-3-(3-fluorophenyl)propanoic acid (CAS No. 117391-51-2): Properties, Applications, and Market Insights

3-Amino-3-(3-fluorophenyl)propanoic acid (CAS 117391-51-2) is a fluorinated amino acid derivative with significant potential in pharmaceutical and biochemical research. This compound, characterized by its 3-fluorophenyl moiety and propanoic acid backbone, has garnered attention due to its unique structural features and versatile applications. Researchers and industry professionals frequently search for "3-Amino-3-(3-fluorophenyl)propanoic acid uses" or "CAS 117391-51-2 supplier," reflecting its growing importance in synthetic chemistry and drug development.

The molecular structure of 3-Amino-3-(3-fluorophenyl)propanoic acid combines a fluorine atom at the meta position of the phenyl ring with an amino acid functional group. This configuration enhances its reactivity and binding affinity, making it valuable for designing enzyme inhibitors or peptide mimetics. Recent studies highlight its role in modulating protein-protein interactions, a hot topic in targeted drug discovery. Searches like "fluorinated amino acids in medicine" or "3-fluorophenyl derivatives applications" demonstrate the compound's relevance in cutting-edge research.

From a synthetic perspective, 117391-51-2 serves as a key intermediate for constructing complex molecules. Its carboxylic acid and primary amine groups allow diverse chemical modifications, addressing popular queries such as "how to modify 3-Amino-3-(3-fluorophenyl)propanoic acid." The fluorine atom's electronegativity influences the compound's metabolic stability, a crucial factor in prodrug design—a trending area in pharmaceutical chemistry.

In material science, this compound contributes to developing fluorescent probes and bioactive polymers. The 3-fluorophenyl group's photophysical properties enable applications in molecular imaging, aligning with searches for "fluorine-containing imaging agents." Its compatibility with solid-phase peptide synthesis (SPPS) also makes it attractive for creating custom peptides, addressing frequent inquiries about "amino acid derivatives for peptide synthesis."

The market for 3-Amino-3-(3-fluorophenyl)propanoic acid reflects increasing demand from contract research organizations (CROs) and academic labs. Analytics reveal spikes in searches for "buy CAS 117391-51-2" alongside related terms like "high-purity fluorinated building blocks." Regulatory-friendly features (non-hazardous classification) further boost its adoption compared to restricted alternatives, as users often seek "safe fluorochemical replacements."

Quality control of 117391-51-2 involves advanced techniques like HPLC and NMR spectroscopy, addressing common concerns about "how to analyze 3-Amino-3-(3-fluorophenyl)propanoic acid purity." Storage recommendations (e.g., anhydrous conditions) frequently appear in technical forums, highlighting practical handling considerations for this hygroscopic compound.

Emerging applications include its use in metal-organic frameworks (MOFs) for catalysis—a trending research area. The compound's ability to coordinate with metals responds to queries about "amino acid-based MOF linkers." Additionally, its role in asymmetric synthesis attracts attention from researchers investigating "chiral auxiliaries for enantioselective reactions."

Environmental and safety profiles of 3-Amino-3-(3-fluorophenyl)propanoic acid are frequently discussed, with searches for "biodegradability of fluorinated amino acids." Its low ecotoxicity distinguishes it from persistent fluorochemicals, aligning with green chemistry principles—a major industry focus. This positions the compound favorably for sustainable fine chemical production.

In conclusion, 3-Amino-3-(3-fluorophenyl)propanoic acid (CAS 117391-51-2) represents a multifaceted tool for modern chemistry. Its balance of synthetic versatility, pharmaceutical relevance, and environmental compatibility ensures continued interest across scientific disciplines, reflected in evolving search trends and research publications.

• 331-25-9(2-(3-Fluorophenyl)acetic acid)
• 60-18-4(L-Tyrosine)
• 51-65-0(2-Amino-3-(4-fluorophenyl)propanoic acid)
• 403-40-7(1-(4-Fluorophenyl)ethanamine)
• 458-09-3(2-(3-fluoro-4-hydroxyphenyl)acetic acid)
• 63-91-2(L-Phenylalanine)
• 325-89-3(3-Amino-3-(4-fluorophenyl)propanoic Acid)
• 405-50-5(4-Fluorophenylacetic acid)
• 366-77-8(4-(4-Fluorophenyl)-4-oxobutanoic Acid)
• 150-30-1(DL-3-Phenylalanine)