5-bromo-4-chloro-3-indolyl phosphate disodium salt
$300.00
CAS No.: 102185-33-1
Catalog No.: 194869
Purity: 95%
MF: C8H4BrClNNa2O4P
MW: 370.434
Storage: 2-8 degree Celsius
SMILES: [Na+].[Na+].P(=O)(OC1=CNC2=CC=C(C(=C12)Cl)Br)([O-])[O-]
Catalog No.: 194869
Purity: 95%
MF: C8H4BrClNNa2O4P
MW: 370.434
Storage: 2-8 degree Celsius
SMILES: [Na+].[Na+].P(=O)(OC1=CNC2=CC=C(C(=C12)Cl)Br)([O-])[O-]
5-bromo-4-chloro-3-indolyl phosphate disodium salt; CAS No.: 102185-33-1; 5-bromo-4-chloro-3-indolyl phosphate disodium salt. PROPERTIES: 5-bromo-4-chloro-3-indolyl phosphate disodium salt is a crystalline solid. Its molecular formula is C8H6BrClNNa2O7P, and the molecular weight is approximately 392.05 g/mol. The compound has a melting point of approximately 140-142 C. It is moderately soluble in water and commonly used in the form of its disodium salt. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing an indole ring, a phosphate group, and halogen atoms, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, 5-bromo-4-chloro-3-indolyl phosphate disodium salt serves as a specialized intermediate. The phosphate group can undergo various reactions such as hydrolysis and alkylation. The indole ring and halogen atoms provide unique electronic effects. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antiviral drugs, the structure of 5-bromo-4-chloro-3-indolyl phosphate disodium salt can be modified to enhance the drug's antiviral activity and pharmacokinetic properties (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as noted in organic chemistry research papers).
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