Cas no 143062-85-5 ((1R,2R)-2-fluorocyclopropanamine;hydrochloride)

(1R,2R)-2-Fluorocyclopropanamine hydrochloride is a chiral cyclopropane derivative featuring a fluorine substituent at the 2-position and an amine group, presented as its stable hydrochloride salt. This compound is of significant interest in medicinal chemistry and asymmetric synthesis due to its rigid cyclopropane scaffold and stereospecific fluorine substitution, which can enhance binding affinity and metabolic stability in bioactive molecules. The (1R,2R) configuration ensures high enantiopurity, making it valuable for the development of pharmaceuticals, particularly in the design of enzyme inhibitors or receptor modulators. Its hydrochloride form improves solubility and handling, facilitating its use in synthetic applications. The compound’s structural features make it a versatile intermediate for drug discovery and fine chemical synthesis.
(1R,2R)-2-fluorocyclopropanamine;hydrochloride structure
143062-85-5 structure
Product Name:(1R,2R)-2-fluorocyclopropanamine;hydrochloride
CAS No:143062-85-5
MF:C3H7ClFN
MW:111.545783281326
MDL:MFCD19205556
CID:3740931
PubChem ID:55281671
Update Time:2025-05-19

(1R,2R)-2-fluorocyclopropanamine;hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Cyclopropanamine, 2-fluoro-, hydrochloride, (1R-trans)-
    • (1R,2R)-2-fluorocyclopropanamine hydrochloride
    • (1R,2R)-2-FLUOROCYCLOPROPANAMINE HCL
    • (1R,2R)-2-fluorocyclopropan-1-amine hydrochloride
    • (1R,2R)-2-fluorocyclopropanamine;hydrochloride
    • 143062-85-5
    • CS3402
    • AS-66161
    • (1R,2R)-2-fluorocyclopropan-1-amine;hydrochloride
    • MFCD19205556
    • MFCD28100743
    • trans-2-Fluorocyclopropanamine hydrochloride
    • 114152-96-4
    • CS3399
    • TRANS-2-FLUOROCYCLOPROPANAMINE HCL
    • EN300-7376533
    • trans-2-fluorocyclopropan-1-amine hydrochloride
    • AKOS006340435
    • CS-0143345
    • rac-(1R,2R)-2-fluorocyclopropan-1-amine hydrochloride
    • DB-200008
    • SCHEMBL9095531
    • MDL: MFCD19205556
    • Inchi: 1S/C3H6FN.ClH/c4-2-1-3(2)5;/h2-3H,1,5H2;1H/t2-,3-;/m1./s1
    • InChI Key: DYTNTYHQHKPQEX-SWLXLVAMSA-N
    • SMILES: Cl.F[C@@H]1C[C@H]1N

Computed Properties

  • Exact Mass: 111.0251051g/mol
  • Monoisotopic Mass: 111.0251051g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 6
  • Rotatable Bond Count: 0
  • Complexity: 46.2
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 2
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 26?2

(1R,2R)-2-fluorocyclopropanamine;hydrochloride Security Information

(1R,2R)-2-fluorocyclopropanamine;hydrochloride Pricemore >>

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Additional information on (1R,2R)-2-fluorocyclopropanamine;hydrochloride

Introduction to (1R,2R)-2-fluorocyclopropanamine;hydrochloride (CAS No. 143062-85-5)

(1R,2R)-2-fluorocyclopropanamine;hydrochloride, identified by the Chemical Abstracts Service Number (CAS No.) 143062-85-5, is a significant compound in the field of pharmaceutical chemistry. This compound has garnered attention due to its unique structural properties and potential applications in drug development. The presence of a fluorine atom in its structure and its chiral configuration make it a subject of intense research interest.

The< strong> fluorine-substituted cyclopropane ring in (1R,2R)-2-fluorocyclopropanamine;hydrochloride introduces unique electronic and steric effects that can influence its biological activity. Fluorine atoms are known to enhance metabolic stability, improve binding affinity, and modulate pharmacokinetic properties of molecules. This makes such compounds valuable scaffolds for designing novel therapeutic agents.

In recent years, there has been a surge in research focusing on fluorinated heterocycles due to their broad spectrum of biological activities. The< strong> cyclopropane moiety is particularly interesting because it introduces rigidity into the molecular structure, which can be exploited to optimize drug-like properties such as solubility, bioavailability, and target interaction.

One of the most compelling aspects of (1R,2R)-2-fluorocyclopropanamine;hydrochloride is its potential in the development of< strong> central nervous system (CNS) drugs. The combination of the fluorine atom and the cyclopropane ring can facilitate blood-brain barrier penetration, a critical factor for many CNS therapeutics. Preclinical studies have shown that fluorinated cyclopropanes can exhibit potent activity against various neurological disorders.

The< strong> hydrochloride salt form of this compound enhances its solubility in water, making it more suitable for formulation into injectable or oral medications. This form is particularly advantageous for drug delivery systems where solubility is a key determinant of efficacy.

Recent advancements in computational chemistry have enabled researchers to predict the binding modes of (1R,2R)-2-fluorocyclopropanamine;hydrochloride with various biological targets with high accuracy. These studies have revealed that the compound can interact with enzymes and receptors involved in pain signaling, inflammation, and neurodegeneration. This has opened up new avenues for developing treatments for conditions such as chronic pain, rheumatoid arthritis, and Alzheimer's disease.

The synthesis of (1R,2R)-2-fluorocyclopropanamine;hydrochloride involves complex organic transformations that require precise control over reaction conditions. The stereochemistry of the compound must be carefully maintained to ensure optimal biological activity. Researchers have developed innovative synthetic routes that utilize asymmetric catalysis to achieve high enantioselectivity, thereby producing the desired enantiomer in high yield.

In addition to its pharmaceutical applications, (1R,2R)-2-fluorocyclopropanamine;hydrochloride has shown promise in materials science. The unique structural features of this compound make it a candidate for developing novel polymers and coatings with enhanced mechanical properties and chemical resistance.

The< strong> future directions of research on (1R,2R)-2-fluorocyclopropanamine;hydrochloride are multifaceted. Scientists are exploring new synthetic methodologies to improve the efficiency and scalability of its production. Furthermore, preclinical and clinical trials are being conducted to evaluate its safety and efficacy in treating various diseases.

The integration of machine learning and artificial intelligence into drug discovery has accelerated the identification of promising candidates like (1R,2R)-2-fluorocyclopropanamine;hydrochloride. These technologies enable rapid screening of large chemical libraries and prediction of biological activity, thereby shortening the time required to bring new drugs to market.

In conclusion, (1R,2R)-2-fluorocyclopropanamine;hydrochloride is a versatile compound with significant potential in pharmaceuticals and materials science. Its unique structural features and biological activities make it a valuable tool for developing novel therapeutics targeting a wide range of diseases. As research continues to uncover new applications for this compound, its importance in science and medicine is likely to grow even further.

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