14227-17-9 | 2,4,6-Trimethoxyaniline

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$10.00	$7.00
250mg	97%	in stock	$19.00	$13.00
1g	97%	in stock	$62.00	$43.00
5g	97%	in stock	$303.00	$212.00

Description

• Catalog Number: AA69906
• Chemical Name: 2,4,6-Trimethoxyaniline
• CAS Number: 14227-17-9
• Molecular Formula: C9H13NO3
• Molecular Weight: 183.2044
• MDL Number: MFCD00017165
• SMILES: COc1cc(OC)c(c(c1)OC)N

Computed Properties

• Complexity: 140
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.2

Upstream Synthesis Route

2,4,6-Trimethoxyaniline, also known as trimethoxybenzenamine, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in organic chemistry due to its unique properties and reactivity.One of the key applications of 2,4,6-Trimethoxyaniline in chemical synthesis is its role as a building block in the creation of complex organic molecules. Due to the presence of three methoxy groups and an amino group on the benzene ring, this compound can participate in a variety of reactions such as nucleophilic aromatic substitution, electrophilic aromatic substitution, and condensation reactions. These reactions enable the incorporation of the 2,4,6-Trimethoxyaniline moiety into larger molecular structures, allowing for the synthesis of a wide range of organic compounds.Furthermore, 2,4,6-Trimethoxyaniline can also serve as a precursor in the synthesis of pharmaceuticals, agrochemicals, and dyes. By modifying the chemical structure of 2,4,6-Trimethoxyaniline through various functional group transformations, chemists can tailor the properties of the resulting molecules for specific applications. This versatility makes 2,4,6-Trimethoxyaniline an essential building block in the pharmaceutical and agrochemical industries, where the development of new compounds with desired properties is paramount.Overall, 2,4,6-Trimethoxyaniline's significance in chemical synthesis lies in its ability to act as a versatile intermediate for the creation of diverse organic compounds, making it a valuable tool for synthetic chemists in the pursuit of novel materials and compounds.

Literature

• Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities.

  Planta medica 20100401