CAS 102185-49-9

1H-Indol-3-ol, 5-bromo-4-chloro-, dihydrogen phosphate (ester), monopotassium salt

Description:

1H-Indol-3-ol, 5-bromo-4-chloro-, dihydrogen phosphate (ester), monopotassium salt, with CAS number 102185-49-9, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of bromine and chlorine substituents at specific positions on the indole ring contributes to its unique reactivity and potential biological activity. As a phosphate ester, it contains a phosphate group that can participate in various biochemical processes, making it relevant in fields such as biochemistry and pharmacology. The monopotassium salt form indicates that it is a potassium salt of the dihydrogen phosphate, which can influence its solubility and stability in aqueous solutions. This compound may exhibit properties such as antimicrobial or antitumor activity, typical of many indole derivatives, and its specific interactions in biological systems can be of interest for research and therapeutic applications.

Formula: C₈H₆BrClNO₄P·K

InChI: InChI=1S/C8H6BrClNO4P.K/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=FVTQASJEJKYYCC-UHFFFAOYSA-N

SMILES: O(P(=O)(O)O)C=1C=2C(NC1)=CC=C(Br)C2Cl.[K]

Synonyms:

• 1H-Indol-3-ol, 5-bromo-4-chloro-, dihydrogen phosphate (ester), monopotassium salt

Potassium 5-bromo-4-chloro-1H-indol-3-yl phosphate

CAS: 102185-49-9

Potassium 5-bromo-4-chloro-1H-indol-3-yl phosphate

Formula: C₈H₄BrClK₂NO₄P

Purity: ≥97%

Molecular weight: 402.65

Ref: 54-OR1106950

Potassium 5-bromo-4-chloro-1H-indol-3-yl phosphate

CAS: 102185-49-9

Formula: C₈H₄BrClK₂NO₄P

Purity: 97%

Molecular weight: 402.6490

Ref: IN-DA0006U1

BCIP dipotassium

CAS: 102185-49-9

BCIP (5-bromo-4-chloro-3-indolyl phosphate) dipotassium is a chromogenic substrate commonly used for the detection of the enzymatic activity of alkaline phosphatase. Upon dephosphorylation by alkaline phosphatase, BCIP produces a blue precipitate, which can be easily visualized. This substrate has various uses, including the detection of gene expression in molecular biology, the identification of alkaline phosphatase activity in clinical pathology, and the detection of protein-protein interactions in biochemistry. Its long-term stability in solution makes it a common choice for many applications.

Formula: C₈H₄BrClK₂NO₄P

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 402.65 g/mol

Ref: 3D-EB110885