CAS 17357-14-1

1H-Indol-3-ol, 5-bromo-, 3-acetate

Description:

1H-Indol-3-ol, 5-bromo-, 3-acetate, with the CAS number 17357-14-1, is a chemical compound that belongs to the indole family, characterized by its bicyclic structure containing a fused benzene and pyrrole ring. This compound features a bromine atom at the 5-position and an acetate group at the 3-position of the indole ring, which influences its reactivity and solubility. It is typically a solid at room temperature and may exhibit moderate to high solubility in organic solvents, depending on the specific conditions. The presence of the bromine substituent can enhance its biological activity, making it of interest in medicinal chemistry and research. Additionally, the acetate group can serve as a protective or activating group in various chemical reactions. The compound may exhibit properties such as fluorescence or UV absorbance, which can be useful in analytical applications. Overall, 1H-Indol-3-ol, 5-bromo-, 3-acetate is a versatile compound with potential applications in pharmaceuticals and organic synthesis.

Formula: C₁₀H₈BrNO₂

InChI: InChI=1S/C10H8BrNO2/c1-6(13)14-10-5-12-9-3-2-7(11)4-8(9)10/h2-5,12H,1H3

InChI key: InChIKey=KFTGECHXNQBTNZ-UHFFFAOYSA-N

SMILES: O(C(C)=O)C=1C=2C(NC1)=CC=C(Br)C2

Synonyms:

• 1H-Indol-3-ol, 5-bromo-, 3-acetate
• 1H-Indol-3-ol, 5-bromo-, acetate (ester)
• 3-Acetoxy-5-bromoindole
• 5-Bromindoxyl acetate
• 5-Bromoindol-3-Yl Acetate
• 5-Bromoindoxyl acetate
• 5-bromo-1H-indol-3-yl acetate
• Indol-3-ol, 5-bromo-, acetate
• Indol-3-ol, 5-bromo-, acetate (ester)
• Indoxyl, 5-bromo-, acetate

5-Bromoindoxyl Acetate

CAS: 17357-14-1

Formula: C₁₀H₈BrNO₂

Purity: >98.0%(HPLC)(N)

Color and Shape: White to Amber to Dark purple powder to crystal

Molecular weight: 254.08

Ref: 3B-A0940

1H-Indol-3-ol, 5-bromo-, 3-acetate

CAS: 17357-14-1

Formula: C₁₀H₈BrNO₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 254.0800

Ref: IN-DA001Z1U

5-Bromoindolyl acetate

CAS: 17357-14-1

5-Bromoindolyl acetate

Purity: 98%

Molecular weight: 254.08g/mol

Ref: 54-BIB1191

5-Bromo-3-indoxyl-3-acetate

CAS: 17357-14-1

5-Bromo-3-indoxyl-3-acetate is a reaction product of 5-bromoindoxyl and acetone. It is activated by the enzyme lipofuscin, which is found in animals. Lipofuscin has been shown to be involved in cell maturation and fatty acid synthesis. 5-Bromo-3-indoxyl-3-acetate stains gland cells that are neutral ph, such as the submandibular gland and proximal tubules of the kidney. The optimum pH for this compound is around 7, which means it can be used at an acidic level with sodium taurocholate. This product stains cells that have been stained with borax carmine.

Formula: C₁₀H₈BrNO₂

Purity: Min. 97.5 Area-%

Color and Shape: Off-White Powder

Molecular weight: 254.08 g/mol

Ref: 3D-FA52314

5-Bromoindoxylacetate extrapure AR, 99%

CAS: 17357-14-1

Formula: C₁₀H₈BrNO₂

Purity: min. 99%

Color and Shape: White to off-white, Crystalline powder

Molecular weight: 254.09

Ref: SR-43675

5-bromo-1H-indol-3-yl acetate

CAS: 17357-14-1

Formula: C₁₀H₈BrNO₂

Purity: 96%

Molecular weight: 254.083

Ref: 10-F373711

5-Bromo-3-indoxylacetate

CAS: 17357-14-1

5-Bromo-3-indoxylacetate acts as an inhibitor of GSK-3, with a pIC50 value of 3.39.

Formula: C₁₀H₈BrNO₂

Color and Shape: Solid

Molecular weight: 254.08

Ref: TM-T205502