Cas no 848649-91-2 (2H-Indole-2-thione,5-bromo-1,3-dihydro-)

2H-Indole-2-thione,5-bromo-1,3-dihydro- structure
848649-91-2 structure
Product Name:2H-Indole-2-thione,5-bromo-1,3-dihydro-
CAS No:848649-91-2
MF:C8H6BrNS
MW:228.108939647675
CID:720595
Update Time:2025-10-29

2H-Indole-2-thione,5-bromo-1,3-dihydro- Chemical and Physical Properties

Names and Identifiers

    • 2H-Indole-2-thione,5-bromo-1,3-dihydro-
    • 2H-INDOLE-2-THIONE, 5-BROMO-1,3-DIHYDRO-
    • 5-Bromoindoline-2-thione
    • Inchi: 1S/C8H6BrNS/c9-6-1-2-7-5(3-6)4-8(11)10-7/h1-3H,4H2,(H,10,11)
    • InChI Key: LYQRCKUBUCCOIE-UHFFFAOYSA-N
    • SMILES: N1C2=C(C=C(Br)C=C2)CC1=S

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Additional information on 2H-Indole-2-thione,5-bromo-1,3-dihydro-

Comprehensive Guide to 2H-Indole-2-thione,5-bromo-1,3-dihydro- (CAS No. 848649-91-2): Properties, Applications, and Market Insights

2H-Indole-2-thione,5-bromo-1,3-dihydro- (CAS No. 848649-91-2) is a specialized organic compound that has garnered significant attention in pharmaceutical and materials science research. This brominated indole derivative features a unique thione functional group, making it particularly valuable for various synthetic applications. Researchers and industry professionals frequently search for information about this compound's synthesis methods, chemical properties, and potential applications in drug discovery.

The molecular structure of 5-bromo-1,3-dihydro-2H-indole-2-thione contains both indole and thione moieties, which contribute to its interesting chemical behavior. Recent studies have focused on its potential as a building block for more complex molecules, particularly in the development of heterocyclic compounds with biological activity. The presence of the bromine atom at the 5-position makes this compound particularly useful for cross-coupling reactions, a topic of great interest in modern organic chemistry.

From a physicochemical perspective, 2H-Indole-2-thione,5-bromo-1,3-dihydro- typically appears as a crystalline solid with moderate solubility in common organic solvents. Its molecular weight and structural features make it suitable for various spectroscopic characterization techniques, including NMR and mass spectrometry. Researchers often inquire about its stability under different conditions and optimal storage requirements, which are crucial considerations for laboratory use.

In pharmaceutical research, this compound has shown promise as a precursor for bioactive molecules. The indole-thione scaffold is particularly interesting for medicinal chemists exploring enzyme inhibitors and receptor modulators. Recent publications have investigated its potential in developing compounds with antioxidant properties and neuroprotective effects, aligning with current trends in neurodegenerative disease research.

The synthetic chemistry community has developed several efficient routes to produce 848649-91-2, with methods ranging from direct bromination of indole precursors to multi-step synthesis from simpler starting materials. These synthetic approaches are frequently discussed in academic forums and patent literature, reflecting the compound's importance in organic synthesis strategies.

Market analysis indicates growing demand for 2H-Indole-2-thione,5-bromo-1,3-dihydro- among contract research organizations and pharmaceutical companies. Suppliers typically offer this compound in research quantities, with purity levels ranging from 95% to 99%. Quality control parameters such as HPLC purity and residual solvent content are critical factors that buyers consider when sourcing this material.

From a regulatory standpoint, CAS 848649-91-2 is generally classified as a research chemical with no significant restrictions in most jurisdictions. However, researchers should always verify local regulations before procurement or use. The compound's material safety data sheet provides essential information about proper handling procedures and personal protective equipment requirements.

Recent advances in computational chemistry have enabled better understanding of 2H-Indole-2-thione,5-bromo-1,3-dihydro-'s molecular properties. Density functional theory (DFT) calculations have provided insights into its electronic structure and reactivity patterns, information that's valuable for designing new derivatives. These computational approaches complement traditional experimental methods in chemical research.

The compound's potential extends beyond pharmaceuticals into materials science applications. Its conjugated system and heteroatom content make it interesting for developing organic semiconductors and photovoltaic materials. These applications align with current global interests in sustainable energy solutions and green chemistry initiatives.

Analytical chemists have developed robust methods for characterizing 5-bromo-1,3-dihydro-2H-indole-2-thione and its derivatives. Techniques such as high-resolution mass spectrometry and X-ray crystallography have been employed to confirm its structure and purity. These analytical methods are crucial for quality control in both research and potential scale-up processes.

Future research directions for 848649-91-2 may explore its incorporation into metal-organic frameworks (MOFs) or as a ligand in coordination chemistry. The compound's donor atoms (sulfur and nitrogen) present opportunities for creating novel coordination complexes with interesting properties. Such developments could open new avenues in catalysis and sensor technology.

For researchers working with 2H-Indole-2-thione,5-bromo-1,3-dihydro-, proper waste disposal procedures should be followed according to institutional guidelines. While the compound doesn't fall under stringent hazardous classifications, responsible laboratory practices should always be maintained. Many institutions provide specific protocols for handling brominated organic compounds like this one.

The intellectual property landscape surrounding CAS 848649-91-2 includes several patents describing its synthesis and applications. Companies interested in commercializing products derived from this compound should conduct thorough patent searches to avoid infringement. The patent literature also serves as a valuable resource for understanding potential industrial applications.

Academic interest in 5-bromo-1,3-dihydro-2H-indole-2-thione continues to grow, with new publications appearing regularly in peer-reviewed journals. Researchers can stay updated through databases that track chemical literature, ensuring they have access to the latest findings about this compound's properties and potential uses.

In conclusion, 2H-Indole-2-thione,5-bromo-1,3-dihydro- (CAS No. 848649-91-2) represents an important building block in modern chemical research. Its unique combination of structural features and reactivity makes it valuable for diverse applications ranging from pharmaceutical development to advanced materials. As research continues, we can expect to see new discoveries and applications emerging for this versatile compound.

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