AD

2-[(E)-{3,3'-Dichloro-4'-[(E)-{1-[(2,4-dimethylphenyl)amino]-1,3-dioxo-2-butanyl}diazenyl]-4-biphenylyl}diazenyl]-N-(2-methoxyphenyl)-3-oxobutanamide(CAS: 68610-86-6)

2-[(E)-{3,3'-Dichloro-4'-[(E)-{1-[(2,4-dimethylphenyl)amino]-1,3-dioxo-2-butanyl}diazenyl]-4-biphenylyl}diazenyl]-N-(2-methoxyphenyl)-3-oxobutanamide
CAS Number

Related Products

Other Suppliers for 2-[(E)-{3,3'-Dichloro-4'-[(E)-{1-[(2,4-dimethylphenyl)amino]-1,3-dioxo-2-butanyl}diazenyl]-4-biphenylyl}diazenyl]-N-(2-methoxyphenyl)-3-oxobutanamide

Basic Information

Molecular Formula
C35H32Cl2N6O5
Molecular Weight
687.58 g/mol
EINECS
271-878-2

Physical Properties

Density
1.26g/cm3 at 20℃

Chemical Identifiers

SMILES
CC1=CC(=C(C=C1)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)C3=CC(=C(C=C3)N=NC(C(=O)C)C(=O)NC4=CC=CC=C4OC)Cl)Cl)C
InChIKey
HKBCNTJSSROSSO-IZRQRQPJSA-N

Database References

FAQ

The compound is a solid with a high molecular weight, approximately 768.6 g/mol. It has a low solubility in water but is more soluble in organic solvents like dichloromethane. Chemically, it is highly reactive, particularly towards nucleophiles and reducing agents. It exhibits diazo chemistry and amide functionality, which contribute to its reactivity. The compound is prone to decomposition under basic conditions.
The compound is synthesized via a multi-step process involving diazotization, coupling, and amidation reactions. Key steps include the diazotization of a phenolic compound, followed by coupling with a diazo derivative to form the desired biphenyl structure. Amide formation is achieved through condensation with a suitable amine derivative. This process often requires careful control of pH and temperature to ensure high yield and selectivity.
This compound is primarily used in the pharmaceutical industry for its diazo and amide functionalities, which are useful in medicinal chemistry. It can also be found in the polymer industry for its potential as a monomer or additive. In the semiconductor industry, it may serve as a precursor or intermediate due to its chemical reactivity. Additionally, it could be used in sensor technology for its ability to respond to specific chemical environments.
When handling this compound, it is essential to use proper personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a fume hood to minimize exposure to air. Due to its diazo and amide functionalities, it is highly reactive and can decompose under basic conditions, so avoid contact with bases and moisture. Ensure that all spills are handled according to the Material Safety Data Sheet (MSDS) and local regulations.

Safety Notice

Please verify product specifications and safety data before use. Contact the supplier for detailed safety information.

Always follow proper handling procedures

Contact Information

Email

roadtrade@roadyes.com