Cas no 108249-43-0 (Methyl 3-bromo-4-hydroxy-5-methoxybenzoate)

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate is a brominated aromatic ester with a molecular formula of C9H9BrO4. This compound features a benzoate core substituted with bromo, hydroxy, and methoxy functional groups, making it a versatile intermediate in organic synthesis. Its reactive sites allow for further functionalization, particularly in pharmaceutical and agrochemical applications. The presence of both electron-donating (methoxy) and electron-withdrawing (bromo) groups enhances its utility in cross-coupling reactions and as a building block for complex molecules. The compound exhibits moderate stability under standard conditions, facilitating handling and storage. Its well-defined structure and purity make it suitable for research and industrial-scale synthesis.
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate structure
108249-43-0 structure
Product Name:Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
CAS No:108249-43-0
MF:C9H9BrO4
MW:261.069362401962
MDL:MFCD06203663
CID:127867
PubChem ID:11402737
Update Time:2025-10-28

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate Chemical and Physical Properties

Names and Identifiers

    • Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
    • Benzoic acid,3-bromo-4-hydroxy-5-methoxy-, methyl ester
    • 3-Brom-4-hydroxy-5-methoxy-benzoesaeure-methylester
    • 3-bromo-4-hydroxy-5-methoxy-benzoic acid methyl ester
    • RARECHEM AL BF 0099
    • Methyl 5-bromo-4-hydroxy-3-methoxybenzoate
    • DTXSID10464816
    • SCHEMBL20604724
    • MFCD06203663
    • Methyl3-bromo-4-hydroxy-5-methoxybenzoate
    • BS-25511
    • AKOS015834197
    • 108249-43-0
    • CS-0211424
    • trans-tert-butyl 6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate
    • G70079
    • SY361041
    • MDL: MFCD06203663
    • Inchi: 1S/C9H9BrO4/c1-13-7-4-5(9(12)14-2)3-6(10)8(7)11/h3-4,11H,1-2H3
    • InChI Key: UIWBPQDQVILUJA-UHFFFAOYSA-N
    • SMILES: BrC1=CC(C(=O)OC)=CC(=C1O)OC

Computed Properties

  • Exact Mass: 259.96800
  • Monoisotopic Mass: 259.96842g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 209
  • 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: 5
  • XLogP3: 2.1
  • Topological Polar Surface Area: 55.8?2

Experimental Properties

  • PSA: 55.76000
  • LogP: 1.94990

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate Customs Data

  • HS CODE:2918990090
  • Customs Data:

    China Customs Code:

    2918990090

    Overview:

    2918990090. Other additional oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
M295488-100mg
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0
100mg
$64.00 2023-05-18
TRC
M295488-250mg
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0
250mg
$75.00 2023-05-18
TRC
M295488-500mg
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0
500mg
$87.00 2023-05-18
TRC
M295488-1g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0
1g
$98.00 2023-05-18
Ambeed
A804191-1g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0 97%
1g
$56.0 2024-04-26
Ambeed
A804191-5g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0 97%
5g
$195.0 2024-04-26
Ambeed
A804191-25g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate
108249-43-0 97%
25g
$680.0 2024-04-26
abcr
AB272202-1 g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate, 97%; .
108249-43-0 97%
1g
€169.50 2023-04-26
abcr
AB272202-5 g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate, 97%; .
108249-43-0 97%
5g
€424.50 2023-04-26
abcr
AB272202-25 g
Methyl 3-bromo-4-hydroxy-5-methoxybenzoate, 97%; .
108249-43-0 97%
25g
€1062.00 2023-04-26

Additional information on Methyl 3-bromo-4-hydroxy-5-methoxybenzoate

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate (CAS No. 108249-43-0): A Comprehensive Overview

Methyl 3-bromo-4-hydroxy-5-methoxybenzoate, identified by its CAS number 108249-43-0, is a significant compound in the realm of chemical and pharmaceutical research. This compound, featuring a benzoate core with bromine, hydroxyl, and methoxy substituents, has garnered attention due to its versatile applications in synthetic chemistry and potential biological activities. The unique structural attributes of Methyl 3-bromo-4-hydroxy-5-methoxybenzoate make it a valuable intermediate in the development of various pharmacological agents.

The benzoate moiety is a well-known pharmacophore in medicinal chemistry, contributing to the solubility and bioavailability of many drugs. The presence of bromine and hydroxyl groups introduces additional reactivity, enabling diverse functionalization pathways. These features are particularly useful in the synthesis of more complex molecules, such as inhibitors and agonists targeting specific biological pathways. Recent advancements in drug discovery have highlighted the importance of such intermediates in developing novel therapeutic agents.

In recent years, researchers have been exploring the potential of Methyl 3-bromo-4-hydroxy-5-methoxybenzoate in the synthesis of bioactive compounds. For instance, studies have demonstrated its utility in creating derivatives with antimicrobial and anti-inflammatory properties. The bromine substituent, in particular, has been shown to enhance binding affinity to certain protein targets, making it an attractive scaffold for drug design. This has led to several innovative approaches in medicinal chemistry, where Methyl 3-bromo-4-hydroxy-5-methoxybenzoate serves as a key building block.

The hydroxyl group in the molecule also plays a crucial role in its reactivity and biological activity. Hydroxylated benzoates are known to exhibit various pharmacological effects, including antioxidant and anti-proliferative properties. The methoxy group further modulates the electronic properties of the molecule, influencing its interactions with biological targets. These structural features collectively contribute to the compound's potential as a precursor for developing new drugs.

One of the most compelling aspects of Methyl 3-bromo-4-hydroxy-5-methoxybenzoate is its versatility in synthetic chemistry. It can be easily modified through various chemical reactions, such as nucleophilic aromatic substitution and etherification, allowing researchers to tailor its properties for specific applications. This flexibility has been exploited in several recent studies aimed at developing novel therapeutic agents. For example, researchers have used this compound to synthesize derivatives with enhanced efficacy against certain diseases.

The pharmaceutical industry has also shown interest in Methyl 3-bromo-4-hydroxy-5-methoxybenzoate due to its potential as a lead compound for drug development. Its structural framework aligns well with several drug targets, making it a promising candidate for further investigation. Preclinical studies have begun to explore its pharmacokinetic and pharmacodynamic properties, providing insights into its potential therapeutic applications. These studies are crucial for understanding how the compound behaves within biological systems and identifying its most promising uses.

In conclusion, Methyl 3-bromo-4-hydroxy-5-methoxybenzoate (CAS No. 108249-43-0) is a multifaceted compound with significant potential in chemical synthesis and pharmaceutical research. Its unique structural features make it an invaluable intermediate for developing novel bioactive molecules. As research continues to uncover new applications for this compound, it is likely to play an increasingly important role in the discovery and development of next-generation therapeutics.

Recommended suppliers
煙臺(tái)朗裕新材料科技有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Xiamen PinR Bio-tech Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Xiamen PinR Bio-tech Co., Ltd.
Beyond Pharmaceutical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shandong Feiyang Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Feiyang Chemical Co., Ltd