Cas no 1047620-84-7 (4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride)

4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride is a chiral amine-alcohol compound with a reactive diene structure, making it a versatile intermediate in organic synthesis. Its hydrochloride salt form enhances stability and solubility, facilitating handling in synthetic applications. The presence of both amino and hydroxyl functional groups enables its use in asymmetric catalysis, pharmaceutical derivatization, and polymer chemistry. The diene moiety offers potential for Diels-Alder reactions, expanding its utility in cycloaddition chemistry. This compound is particularly valuable for researchers developing bioactive molecules or fine chemicals requiring precise stereochemical control. Its bifunctional nature allows for selective modifications, making it a useful building block in complex molecular architectures.
4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride structure
1047620-84-7 structure
Product Name:4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride
CAS No:1047620-84-7
MF:C9H18ClNO
MW:191.698321819305
MDL:MFCD03129304
CID:1067201
PubChem ID:16189278
Update Time:2025-10-17

4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 4-(1-Amino-ethyl)-hepta-1,6-dien-4-ol hydrochloride
    • 4-(1-aminoethyl)hepta-1,6-dien-4-ol;hydrochloride
    • 4-(1-aminoethyl)hepta-1,6-dien-4-ol hydrochloride
    • 4-(1-Aminoethyl)-1,6-heptadien-4-ol hydrochloride
    • 1047620-84-7
    • CS-0329770
    • MFCD03129304
    • BS-37186
    • MLS000718383
    • 4-(1-aminoethyl)hepta-1,6-dien-4-olhydrochloride
    • SB84550
    • SMR000290651
    • 4-(1-Aminoethyl)-1,6-heptadien-4-ol HCl
    • CHEMBL1897684
    • AKOS003725895
    • 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride
    • MDL: MFCD03129304
    • Inchi: 1S/C9H17NO.ClH/c1-4-6-9(11,7-5-2)8(3)10;/h4-5,8,11H,1-2,6-7,10H2,3H3;1H
    • InChI Key: MEDOFOOUSBXHJP-UHFFFAOYSA-N
    • SMILES: Cl.OC(CC=C)(CC=C)C(C)N

Computed Properties

  • Exact Mass: 191.1076919g/mol
  • Monoisotopic Mass: 191.1076919g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 5
  • Complexity: 133
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 46.2?2

4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB215611-1 g
4-(1-Aminoethyl)-1,6-heptadien-4-ol hydrochloride; 95%
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€94.10 2023-06-23
abcr
AB215611-5 g
4-(1-Aminoethyl)-1,6-heptadien-4-ol hydrochloride; 95%
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AB215611-25 g
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AB215611-50 g
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B402213-10mg
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Additional information on 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride

Comprehensive Overview of 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride (CAS No. 1047620-84-7)

4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride (CAS No. 1047620-84-7) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its unique aminoethyl and heptadienol functional groups, exhibits versatile reactivity, making it a valuable intermediate in synthetic chemistry. Researchers often explore its potential in drug discovery, particularly in the development of novel bioactive molecules and small-molecule inhibitors. Its structural features, including the hydrochloride salt form, enhance solubility and stability, which are critical for laboratory applications.

In recent years, the demand for 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride has surged due to its relevance in medicinal chemistry and bioconjugation techniques. A common query among scientists is: "What are the synthetic routes for 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride?" The compound is typically synthesized via multi-step organic reactions, including reductive amination and alcohol protection-deprotection strategies. Its CAS No. 1047620-84-7 serves as a unique identifier in chemical databases, ensuring accurate sourcing and regulatory compliance.

The compound's diene moiety offers opportunities for click chemistry applications, a trending topic in drug delivery systems and biomaterial engineering. Researchers investigating "How does 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride interact with biological targets?" have reported its potential as a ligand or scaffold for protein binding studies. Additionally, its hydrophilic-lipophilic balance makes it suitable for formulations in nanotechnology and controlled-release therapies.

From an industrial perspective, 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride is often discussed in the context of green chemistry and sustainable synthesis. Questions like "Is there an eco-friendly method to produce 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride?" highlight the growing emphasis on reducing environmental impact. Recent advancements in catalytic processes and solvent-free reactions have addressed these concerns, aligning with global ESG (Environmental, Social, and Governance) goals.

Analytical characterization of CAS No. 1047620-84-7 involves techniques such as NMR spectroscopy, mass spectrometry, and HPLC purity testing. These methods ensure batch-to-batch consistency, a critical factor for high-throughput screening in drug development. The compound's stability under various pH conditions is another area of interest, particularly for formulation scientists optimizing oral bioavailability.

In summary, 4-(1-Aminoethyl)-1,6-heptadien-4-ol Hydrochloride (CAS No. 1047620-84-7) represents a multifaceted tool for modern research. Its applications span from peptide mimetics to polymer chemistry, reflecting the compound's adaptability. As the scientific community continues to explore its potential, this molecule remains a subject of innovation and discovery.

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