5369-19-7 | 3-(tert-Butyl)aniline

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$20.00	$14.00
10g	98%	in stock	$24.00	$17.00
25g	98%	in stock	$59.00	$41.00
100g	98%	in stock	$233.00	$163.00

Description

• Catalog Number: AB65569
• Chemical Name: 3-(tert-Butyl)aniline
• CAS Number: 5369-19-7
• Molecular Formula: C10H15N
• Molecular Weight: 149.2328
• MDL Number: MFCD00125078
• SMILES: Nc1cccc(c1)C(C)(C)C

Computed Properties

• Complexity: 123
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.7

Upstream Synthesis Route

3-(tert-Butyl)aniline, also known as N,N-di-tert-butylaniline, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable intermediate in various reactions and processes.In chemical synthesis, 3-(tert-Butyl)aniline serves as an important building block for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its tert-butyl group provides steric hindrance, which can influence the reactivity and selectivity of reactions it participates in.One key application of 3-(tert-Butyl)aniline is in the synthesis of dyes and pigments. The presence of the aniline moiety allows for the formation of vibrant and stable colorants through various coupling reactions. Additionally, the tert-butyl group can enhance the color strength and lightfastness of the final products.Furthermore, 3-(tert-Butyl)aniline is utilized in the production of polymers and polymer additives. Its compatibility with different polymerization processes enables the modification of polymer properties such as thermal stability, solubility, and mechanical strength. This compound can act as a chain transfer agent, allowing for control over molecular weight and branching in polymer chains.Overall, the versatility of 3-(tert-Butyl)aniline in chemical synthesis makes it a valuable component in the development of a wide range of functional materials with diverse applications in industries such as pharmaceuticals, textiles, and plastics.

Literature

• Enantioselective fluorescence sensing of chiral alpha-amino alcohols.

  The Journal of organic chemistry 20080606