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CAS 102185-33-1

:

5-Bromo-4-chloro-3-indolyl phosphate disodium salt

Description:
5-Bromo-4-chloro-3-indolyl phosphate disodium salt, with the CAS number 102185-33-1, is a synthetic organic compound commonly used as a substrate in biochemical assays, particularly in the detection of phosphatase activity. This compound features an indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring, and is substituted with bromine and chlorine atoms, enhancing its reactivity. The phosphate group in its structure makes it a phosphate donor, which is crucial for enzymatic reactions involving phosphatases. As a disodium salt, it is soluble in water, facilitating its use in various laboratory applications. The compound is often employed in histochemical staining techniques, allowing for the visualization of enzyme activity in tissues or cells. Its stability and specificity make it a valuable tool in molecular biology and biochemistry research. Safety precautions should be observed when handling this compound, as with any chemical reagent, to minimize exposure and ensure proper laboratory practices.
Formula:C8H6BrClNO4P·2Na
InChI:InChI=1S/C8H6BrClNO4P.2Na/c9-4-1-2-5-7(8(4)10)6(3-11-5)15-16(12,13)14;;/h1-3,11H,(H2,12,13,14);;
InChI key:InChIKey=NHDSSFOCCPJFRE-UHFFFAOYSA-N
SMILES:O(P(=O)(O)O)C=1C=2C(NC1)=CC=C(Br)C2Cl.[Na]
Synonyms:
  • 1H-Indol-3-ol, 5-bromo-4-chloro-, 3-(dihydrogen phosphate), sodium salt (1:2)
  • 1H-Indol-3-ol, 5-bromo-4-chloro-, dihydrogen phosphate (ester), disodium salt
  • 5-Bromo-4-chloro-3-indolyl phosphate, disodium salt, hydrate
  • BCIP-2Na
  • 5-Bromo-4-Chloro-3-Indolyl Phosphate Disodium Salt
  • 5-Bromo-4-chloro-3-indolyl phosphate disodium salt
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