773-63-7

Basic information

• Product Name: 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE
• Synonyms: 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE;2,3,3-TriMethyl-3H-indol-5-aMine
• CAS NO: 773-63-7
• Molecular Formula: C₁₁H₁₄N₂
• Molecular Weight: 174.24
• Mol File: 773-63-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: 178 °C
• Boiling Point: 309.8±42.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 6.48±0.60(Predicted)
• CAS DataBase Reference: 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE(773-63-7)
• EPA Substance Registry System: 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE(773-63-7)

Safety Data

• Hazardous Substances Data: 773-63-7(Hazardous Substances Data)

Usage

General Description

5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE is a chemical compound with the molecular formula C11H14N2. It is a derivative of indole, which is a heterocyclic aromatic organic compound. This particular compound contains an amino group (NH2) and three methyl groups attached to the indole ring. It is used in the synthesis of pharmaceuticals and agrochemicals, as well as in research and development. The compound has potential biological activity and is of interest in medicinal chemistry for its potential pharmacological properties. Its precise applications and properties depend on the specific context and formulation in which it is used.

Upstream product

• 3484-22-8 2,3,3-trimethyl-5-nitro-3H-indole 
• 60-29-7 diethyl ether 

Downstream Products

• 1355342-75-4 C₃₀H₃₈N₃O⁽¹⁺⁾*Cl^(1-) 
• 93272-84-5 5-amino-3,3-dimethyl-2-p-nitrostyryl-3H-indole 
• 93272-83-4 2,3,3-trimethyl-5-(p-nitrobenzylidene)amino-3H-indole 
• 97315-57-6 5-(4'-methoxybenzyloxy)benzylidenamine-2,3,3-trimethylindolenine 

Relevant articles and documents

NOVEL SQUARYLIUM COMPOUNDS, AND COMPOSITIONS COMPRISING SAME

The present disclosure is disclosed herein. The present invention relates to a novel squarylium compound and a near infrared absorbing resin composition containing the squarylium compound.

LABELS, THEIR PRODUCTION PROCESS AND THEIR USES

Labels are disclosed capable of forming a covalent or non-covalent bond with a target molecule, particularly a biological molecule. The structure of these labels may consist of a dye covalently bound by one or more carbons on its chemical structure to one or more [FUNC] group(s), and optionally one or more [SOL] group(s). The structure of these labels allow selection of dyes from a wide variety of different excitation and emission wavelengths and allow easy functionalization of the dye without appreciably altering its spectral characteristics or its solubility characteristics.

NEW DYE COMPOUNDS

The present disclosure provides compounds that may be used as chromogens, fluorochromes, or as both. Said compounds may further be used as substrate for at least one enzyme, wherein said enzyme is capable of processing an aromatic amine group (—NH2), an aromatic hydroxyl group (—OH), or an aromatic phosphate group (—PO4). Furthermore, the present disclosure also provides methods for precipitating said compounds as well as methods for detecting a target using said compounds. Even further, kits comprising said compounds are disclosed. Said compounds may be used in any method utilizing a fluorochrome, a chromogen, or both.