341-58-2 | 2,2'-Bis(trifluoromethyl)benzidine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$9.00	$6.00
10g	98%	in stock	$12.00	$8.00
25g	98%	in stock	$27.00	$19.00
100g	98%	in stock	$79.00	$56.00
500g	98%	in stock	$283.00	$198.00

Description

• Catalog Number: AB59569
• Chemical Name: 2,2'-Bis(trifluoromethyl)benzidine
• CAS Number: 341-58-2
• Molecular Formula: C14H10F6N2
• Molecular Weight: 320.2330191999999
• MDL Number: MFCD00190155
• SMILES: Nc1ccc(c(c1)C(F)(F)F)c1ccc(cc1C(F)(F)F)N

Computed Properties

• Complexity: 345
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 8
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 4

Upstream Synthesis Route

In chemical synthesis, 2,2'-Bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine, also known as $name$, serves as a versatile building block due to its unique chemical properties. This compound is commonly utilized as a key intermediate in the production of high-performance polymers, specifically in the creation of polyimides and other specialty materials.$name$ plays a crucial role in the synthesis of novel polymers with exceptional thermal stability, mechanical strength, and chemical resistance. Its trifluoromethyl groups provide increased hydrophobicity and electron-withdrawing capabilities, contributing to the overall enhanced properties of the resulting polymers. Additionally, the rigid biphenyl backbone of $name$ imparts structural integrity and dimensional stability to the final polymer products.Furthermore, the presence of the diamine moiety in $name$ enables it to participate in various polymerization reactions, such as step-growth polymerizations, providing control over the molecular weight and chain architecture of the polymers. This versatility allows for the tailoring of polymer properties to meet specific application requirements in industries ranging from aerospace to electronics.Overall, the strategic incorporation of 2,2'-Bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine in chemical synthesis offers a valuable route to the development of advanced materials with a wide range of industrial applications.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501