Cas no 129541-43-1 (5-Bromo-4-chloro-1H-indol-3-yl Butanoate)

5-Bromo-4-chloro-1H-indol-3-yl butanoate is a halogenated indole derivative with applications in organic synthesis and pharmaceutical research. This compound features a bromo-chloro substitution pattern on the indole core, enhancing its reactivity and utility in cross-coupling reactions or as a building block for bioactive molecules. The butanoate ester group improves solubility in organic solvents, facilitating further derivatization. Its structural features make it valuable for developing enzyme inhibitors, fluorescent probes, or agrochemical intermediates. The product is characterized by high purity and stability under standard storage conditions, ensuring reliable performance in synthetic workflows. Careful handling is recommended due to potential sensitivity to light and moisture.
5-Bromo-4-chloro-1H-indol-3-yl Butanoate structure
129541-43-1 structure
Product Name:5-Bromo-4-chloro-1H-indol-3-yl Butanoate
CAS No:129541-43-1
MF:C12H11BrClNO2
MW:316.578241586685
MDL:MFCD00083261
CID:219336
PubChem ID:688404
Update Time:2025-06-11

5-Bromo-4-chloro-1H-indol-3-yl Butanoate Chemical and Physical Properties

Names and Identifiers

    • 5-Bromo-4-chloro-1H-indol-3-yl butyrate
    • (5-bromo-4-chloro-1H-indol-3-yl)butanoate
    • 5-BROMO-4-CHLORO-(1H-INDOL-3-YL) BUTANOATE
    • 5-BroMo-4-chloro-3-indolyl butyrate
    • 5-Bromo-4-chloro-3-indoxyl butyrate
    • Bacteria chromogenic substrate-1
    • Butanoic acid,5-bromo-4-chloro-1H-indol-3-yl ester
    • X-BUTYRATE
    • 5-BROMO-4-CHLOROINDOXYLBUTYRATE
    • 5-Bromo-4-chloro-(1H-indol-3-yl) butyrate
    • 5-Bromo-4-chloro-3-indoxyl butyrateX-Butyrate
    • Butanoic acid, 5-broMo-4-chloro-1H-indol-3-yl ester
    • 5-Bromo-4-chloro-3-indolyl butyrate, >=99%
    • SCHEMBL1614924
    • (5-bromo-4-chloro-1H-indol-3-yl) butanoate
    • FT-0620121
    • AS-68946
    • 5-bromo-4-chloro-1H-indol-3-yl butanoate
    • DTXSID00350895
    • B-7050
    • HY-78639
    • 129541-43-1
    • A888844
    • H10237
    • CS-M2349
    • AMY41486
    • MFCD00083261
    • AKOS022180540
    • PD078545
    • 5-Bromo-4-chloro-1H-indol-3-yl Butanoate
    • MDL： MFCD00083261
    • Inchi： 1S/C12H11BrClNO2/c1-2-3-10(16)17-9-6-15-8-5-4-7(13)12(14)11(8)9/h4-6,15H,2-3H2,1H3
    • InChI Key： UKTKOBRRRRODGL-UHFFFAOYSA-N
    • SMILES： BrC1C=CC2=C(C=1Cl)C(=CN2)OC(CCC)=O

Computed Properties

  • Exact Mass: 314.96600
  • Monoisotopic Mass: 314.96617g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 4
  • Complexity: 290
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3.9
  • Topological Polar Surface Area: 42.1?2

Experimental Properties

  • Color/Form: White powder
  • Melting Point: 91-93 °C
  • PSA: 42.09000
  • LogP: 4.28930
  • Solubility: Insoluble in water

5-Bromo-4-chloro-1H-indol-3-yl Butanoate Security Information

  • WGK Germany：3
  • Hazard Category Code： 22-41
  • Safety Instruction： S24/25
  • Hazardous Material Identification： Xn
  • Safety Term：S24/25

5-Bromo-4-chloro-1H-indol-3-yl Butanoate Customs Data

  • HS CODE：2933990090
  • Customs Data：

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. 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, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

5-Bromo-4-chloro-1H-indol-3-yl Butanoate Pricemore >>

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5-Bromo-4-chloro-1H-indol-3-yl Butanoate Suppliers

Shenzhen GeneSeqTools Bioscience & Technology Co. Ltd.
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(CAS:129541-43-1)5-Bromo-4-chloro-3-indolyl butyrate
Order Number:G02030001
Stock Status:in Stock
Quantity:1g;5g;25g
Purity:98%
Pricing Information Last Updated:Monday, 4 August 2025 16:35
Price ($):inquiry

5-Bromo-4-chloro-1H-indol-3-yl Butanoate Related Literature

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Additional information on 5-Bromo-4-chloro-1H-indol-3-yl Butanoate

Comprehensive Overview of 5-Bromo-4-chloro-1H-indol-3-yl Butanoate (CAS No. 129541-43-1)

5-Bromo-4-chloro-1H-indol-3-yl Butanoate (CAS No. 129541-43-1) is a synthetic indole derivative that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its unique bromo and chloro substitutions on the indole ring, serves as a versatile intermediate in the synthesis of bioactive molecules. Researchers are particularly interested in its potential applications in drug discovery, owing to its structural similarity to naturally occurring indole alkaloids, which are known for their diverse biological activities.

The growing interest in 5-Bromo-4-chloro-1H-indol-3-yl Butanoate aligns with current trends in precision medicine and targeted therapy. As the scientific community explores novel ways to combat complex diseases, compounds like this are being investigated for their ability to modulate specific biochemical pathways. For instance, indole derivatives are frequently studied for their roles in enzyme inhibition and receptor binding, making them valuable tools in the development of new therapeutics.

One of the most frequently asked questions about 5-Bromo-4-chloro-1H-indol-3-yl Butanoate revolves around its synthetic methodology. Researchers often search for optimized protocols to produce this compound with high yield and purity. Recent advancements in green chemistry have also sparked interest in eco-friendly synthesis routes, minimizing hazardous byproducts and reducing environmental impact. This aligns with the broader industry shift toward sustainable chemistry practices.

Another hot topic is the compound's potential role in neuropharmacology. Indole derivatives are known to interact with serotonin receptors, which are critical in treating neurological disorders. While 5-Bromo-4-chloro-1H-indol-3-yl Butanoate itself is not a drug, its structural features make it a promising scaffold for designing central nervous system (CNS)-targeting molecules. This has led to increased demand from academic and industrial labs specializing in neurodegenerative disease research.

From a commercial perspective, the global market for specialized indole derivatives is expanding rapidly. 5-Bromo-4-chloro-1H-indol-3-yl Butanoate is often listed as a high-purity reference standard for analytical purposes, particularly in HPLC and LC-MS applications. Quality control in pharmaceutical manufacturing relies heavily on such compounds to ensure batch consistency and regulatory compliance.

In summary, 5-Bromo-4-chloro-1H-indol-3-yl Butanoate (CAS No. 129541-43-1) represents a fascinating intersection of medicinal chemistry and biochemical research. Its relevance to contemporary scientific challenges—from drug development to analytical chemistry—ensures its continued importance in modern laboratories. As research progresses, this compound may unlock new possibilities in therapeutic innovation and scientific discovery.

129541-43-1 (5-Bromo-4-chloro-1H-indol-3-yl Butanoate) Related Products

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Shenzhen GeneSeqTools Bioscience & Technology Co. Ltd.
(CAS:129541-43-1)5-Bromo-4-chloro-3-indolyl butyrate
G02030001
Purity:98%
Quantity:1g;5g;25g
Price ($):Inquiry
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