Cas no 805250-54-8 (2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide)

2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide is a heterocyclic organic compound featuring a benzothiazolone core with an amino functional group. Its hydrobromide salt form enhances stability and solubility, making it suitable for synthetic applications in pharmaceutical and agrochemical research. The dihydro structure contributes to its reactivity as an intermediate in the synthesis of more complex molecules, particularly in the development of bioactive compounds. This product is characterized by high purity and consistent performance, ensuring reliable results in coupling reactions and heterocyclic derivatization. Its well-defined crystalline structure facilitates handling and storage, while its compatibility with common organic solvents broadens its utility in diverse experimental conditions.
2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide structure
805250-54-8 structure
Product Name:2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide
CAS No:805250-54-8
MF:C7H9BrN2OS
MW:249.128159284592
CID:1028369
PubChem ID:23111725
Update Time:2025-10-05

2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-5,6-dihydrobenzo[d]thiazol-7(4H)-one hydrobromide
    • 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide
    • 2-amino-5,6-dihydro-4H-1,3-benzothiazol-7-one,hydrobromide
    • 2-AMino-5,6-dihydro-4H-benzothiazol -7-one hydrobroMide
    • QC-8519
    • AKOS015994822
    • 805250-54-8
    • 2-Amino-5,6-dihydrobenzo[d]thiazol-7(4H)-onehydrobromide
    • 2-amino-5,6-dihydro-4H-1,3-benzothiazol-7-one;hydrobromide
    • G10045
    • SCHEMBL3450128
    • 2-Amino-5,6-dihydro-1,3-benzothiazol-7(4H)-one--hydrogen bromide (1/1)
    • 2-Amino-5,6-dihydro-4h-benzothiazol-7-one HBr
    • 2-Amino-5,6-dihydro-4H-benzothiazol-7-one hydrobromide
    • DTXSID90630653
    • 2-AMINO-5,6-DIHYDRO-4H-1,3-BENZOTHIAZOL-7-ONE HYDROBROMIDE
    • 2-Amino-7-oxo-4,5,6,7-tetrahydrobenzothiazole Hydrobromide;
    • DB-364555
    • Inchi: 1S/C7H8N2OS.BrH/c8-7-9-4-2-1-3-5(10)6(4)11-7;/h1-3H2,(H2,8,9);1H
    • InChI Key: RGIACPTWMIHUNU-UHFFFAOYSA-N
    • SMILES: Br.S1C(N)=NC2=C1C(CCC2)=O

Computed Properties

  • Exact Mass: 247.96200
  • Monoisotopic Mass: 247.96190g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 185
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 84.2?2

Experimental Properties

  • PSA: 84.95000
  • LogP: 2.13250

2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide Customs Data

  • HS CODE:2934200090
  • Customs Data:

    China Customs Code:

    2934200090

    Overview:

    2934200090. Other compounds containing a benzothiazole ring. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934200090. other compounds containing in the structure a benzothiazole ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide Related Literature

Additional information on 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide

Comprehensive Overview of 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide (CAS No. 805250-54-8)

2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide (CAS No. 805250-54-8) is a specialized organic compound widely utilized in pharmaceutical research and fine chemical synthesis. This compound belongs to the benzothiazolone family, a class of heterocyclic compounds known for their diverse biological activities. The presence of the amino group and hydrobromide salt enhances its solubility and stability, making it a valuable intermediate in drug discovery and development.

In recent years, the demand for 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide has surged due to its potential applications in targeting neurodegenerative diseases and metabolic disorders. Researchers are particularly interested in its role as a precursor for designing small molecule inhibitors and kinase modulators. The compound's unique structure allows it to interact with specific enzymes and receptors, making it a focal point in medicinal chemistry and biochemical studies.

One of the trending topics in the scientific community is the exploration of benzothiazolone derivatives for their neuroprotective properties. Studies suggest that compounds like 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide may exhibit antioxidant and anti-inflammatory effects, which are critical in addressing conditions such as Alzheimer's and Parkinson's diseases. This aligns with the growing interest in natural product-inspired drug design and targeted therapy.

From a synthetic perspective, CAS No. 805250-54-8 is often employed in multi-step organic reactions, including cyclization and amination processes. Its versatility as a building block has been highlighted in recent publications, where it serves as a key intermediate for constructing more complex molecular architectures. The compound's hydrobromide form further simplifies purification and handling, which is a significant advantage in laboratory settings.

Another area of interest is the compound's potential role in cancer research. Preliminary studies indicate that benzothiazolone-based compounds may interfere with cellular signaling pathways, offering a novel approach to anticancer drug development. This has led to increased inquiries about structure-activity relationships (SAR) and molecular docking studies involving 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide.

For researchers and manufacturers, the quality and purity of CAS No. 805250-54-8 are paramount. Advanced analytical techniques such as HPLC, NMR, and mass spectrometry are routinely used to verify its identity and ensure compliance with industry standards. The compound's stability under various storage conditions is also a frequently discussed topic, particularly in forums dedicated to chemical storage best practices.

In summary, 2-Amino-5,6-dihydro-7(4H)-benzothiazolone Hydrobromide (CAS No. 805250-54-8) is a compound of significant scientific and industrial relevance. Its applications span from pharmaceutical intermediates to biochemical probes, reflecting the evolving needs of modern research. As the scientific community continues to uncover its potential, this compound is poised to remain a subject of intense study and innovation.

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