Indoline-5,6-diol Hydrobromide TCI D6488

Chemical Identity

Other names: 5,6-Dihydroxyindoline Hydrobromide · 5,6-Indolinediol Hydrobromide
CAS No.: 138937-28-7
PubChem: CID 22020437
Formula: C8H9NO2.HBr
Molecular weight: 232.08 g/mol
Purity: >95.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,3-dihydro-1H-indole-5,6-diol;hydrobromide
SMILES: C1CNC2=CC(=C(C=C21)O)O.Br
InChIKey: TXMQOPNBBITFNX-UHFFFAOYSA-N
MDL: MDL07368401

Rp 2.889.600,00

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Indoline-5,6-diol Hydrobromide is a chemical compound widely used in organic reactions and the synthesis of complex molecules. As a building block in heterocyclic chemistry, it plays a crucial role in the development of new compounds with specific biological activities. This compound is essential in laboratory settings where researchers aim to construct intricate molecular structures. Its unique chemical structure, featuring two hydroxyl groups and one bromide, makes it highly reactive and versatile in various chemical transformations.

The reactivity of Indoline-5,6-diol Hydrobromide is due to its functional groups, which allow it to participate in substitution, reduction, and bond formation reactions. These properties make it a preferred choice for chemists working on drug synthesis and bioactive compound development. Its ability to undergo multiple chemical transformations enhances its utility in both academic and industrial research environments.

In Indonesian laboratories, this compound is commonly used in organic chemistry, pharmacology, and biochemistry research. It supports the synthesis of pharmaceuticals and bioactive molecules, contributing to advancements in drug discovery and molecular design. Many educational and research institutions rely on this compound for experiments requiring complex molecular synthesis.

Related TCI products

Organic synthesis applications benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecular frameworks.
Pharmacological research utilizes it for the development of bioactive compounds, supporting drug discovery and therapeutic innovation.
Biochemical studies often incorporate it in the synthesis of molecules with specific biological functions, enhancing research in molecular biology.
Educational institutions use it in teaching and experimental settings to demonstrate key chemical reactions and molecular construction techniques.
Industrial research laboratories apply it in the development of new chemical products, leveraging its role in heterocyclic compound synthesis.

Brand	TCI
CAS number	138937-28-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard supplier offerings
Physical form	Solid, typically in crystalline or powder form
Storage	Store in a cool, dry place away from moisture and direct sunlight

Indoline-5,6-diol Hydrobromide should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption, which can affect its reactivity and stability. Due to its reactive nature, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Proper storage and handling ensure the compound remains effective for use in various chemical and pharmaceutical applications.

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