Cas no 303070-22-6 (1-(5-Chlorothien-2-yl)propan-1-amine)

1-(5-Chlorothien-2-yl)propan-1-amine is a specialized organic compound featuring a chlorinated thiophene ring linked to a propylamine moiety. This structure imparts unique reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The chlorine substituent enhances electrophilic properties, facilitating further functionalization, while the amine group offers versatility in forming derivatives such as amides or Schiff bases. Its well-defined molecular architecture ensures consistent performance in heterocyclic chemistry applications. The compound is particularly useful in the development of bioactive molecules due to its balanced lipophilicity and electronic effects. Proper handling under controlled conditions is recommended due to its reactive functional groups.
1-(5-Chlorothien-2-yl)propan-1-amine structure
303070-22-6 structure
Product Name:1-(5-Chlorothien-2-yl)propan-1-amine
CAS No:303070-22-6
MF:C7H10ClNS
MW:175.678999423981
MDL:MFCD09778013
CID:3168375
PubChem ID:17249036
Update Time:2025-05-21

1-(5-Chlorothien-2-yl)propan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 1-(5-Chlorothien-2-yl)propan-1-amine
    • 2-Thiophenemethanamine, 5-chloro-a-ethyl-
    • SCHEMBL12261844
    • Z359503512
    • BBL017907
    • AKOS016344015
    • G23287
    • 1-(5-chlorothiophen-2-yl)propan-1-amine
    • AKOS003383147
    • ALBB-002190
    • MFCD09778013
    • STK489640
    • EN300-77366
    • VS-06584
    • 303070-22-6
    • 996-236-5
    • MDL: MFCD09778013
    • Inchi: 1S/C7H10ClNS/c1-2-5(9)6-3-4-7(8)10-6/h3-5H,2,9H2,1H3
    • InChI Key: CQHFAMGIJTYXRN-UHFFFAOYSA-N
    • SMILES: ClC1=CC=C(C(CC)N)S1

Computed Properties

  • Exact Mass: 175.0222482g/mol
  • Monoisotopic Mass: 175.0222482g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 110
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 54.3?2

1-(5-Chlorothien-2-yl)propan-1-amine Pricemore >>

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Additional information on 1-(5-Chlorothien-2-yl)propan-1-amine

Comprehensive Overview of 1-(5-Chlorothien-2-yl)propan-1-amine (CAS No. 303070-22-6): Properties, Applications, and Industry Insights

1-(5-Chlorothien-2-yl)propan-1-amine, identified by its CAS number 303070-22-6, is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound features a unique chlorothiophene backbone coupled with an amine functional group, making it a versatile intermediate for synthesizing bioactive molecules. Its molecular structure, C7H10ClNS, highlights its potential for drug discovery and material science applications, aligning with current trends in green chemistry and sustainable synthesis.

In recent years, the demand for heterocyclic compounds like 1-(5-Chlorothien-2-yl)propan-1-amine has surged due to their role in developing targeted therapies and crop protection agents. Researchers are particularly interested in its structure-activity relationship (SAR), which is critical for optimizing bioavailability and binding affinity in drug design. The compound’s chlorothiophene moiety is also being explored for organic electronics, such as OLEDs and conductive polymers, reflecting broader industry shifts toward functional materials.

From a synthetic perspective, 303070-22-6 is often synthesized via Pd-catalyzed cross-coupling or reductive amination, methods that align with the push for atom-efficient reactions. Analytical techniques like HPLC and NMR spectroscopy are essential for verifying its purity, a topic frequently searched by quality control professionals. Additionally, its logP value and solubility profile are key parameters for formulators, addressing common queries in preclinical development forums.

The compound’s relevance extends to neuroscience research, where its amine group is investigated for modulating neurotransmitter receptors. This connects to trending topics like neurodegenerative disease treatments and psychoactive compound studies, though strictly within legal and ethical boundaries. Environmental considerations are also paramount; studies on its biodegradability and ecotoxicology are increasingly cited in regulatory submissions.

For suppliers and manufacturers, CAS 303070-22-6 represents a niche yet growing market segment. Searchers often look for bulk pricing, technical datasheets, or custom synthesis options, underscoring the need for transparent supply chains. Regulatory compliance, such as REACH and GMP standards, remains a top priority, reflecting industry-wide emphasis on safety protocols and documentation.

In summary, 1-(5-Chlorothien-2-yl)propan-1-amine exemplifies the intersection of cutting-edge chemistry and applied science. Its multifaceted applications—from pharmaceutical intermediates to advanced materials—make it a compound of enduring interest. As research evolves, so too will its role in addressing global challenges in healthcare and sustainability.

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