21089-44-1

Basic information

• Product Name: 2-(carboxy-diphenyl-methyl)disulfanyl-2,2-diphenyl-acetic acid
• CAS NO: 21089-44-1
• Molecular Formula: C₂₈H₂₂O₄S₂
• Molecular Weight: 486.6019
• Mol File: 21089-44-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 626.1°Cat760mmHg
• Flash Point: 332.4°C
• Density: 1.347g/cm³
• CAS DataBase Reference: 2-(carboxy-diphenyl-methyl)disulfanyl-2,2-diphenyl-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(carboxy-diphenyl-methyl)disulfanyl-2,2-diphenyl-acetic acid(21089-44-1)
• EPA Substance Registry System: 2-(carboxy-diphenyl-methyl)disulfanyl-2,2-diphenyl-acetic acid(21089-44-1)

Safety Data

• Hazardous Substances Data: 21089-44-1(Hazardous Substances Data)

Usage

Explanation

This is the scientific name of the compound, which describes its chemical structure.

Explanation

The compound is commonly referred to as Bucillamine, which is a simpler name used in discussions and research.

Explanation

Bucillamine is classified as a pharmaceutical compound, meaning it has potential therapeutic effects and can be used in the development of medications.

Explanation

Bucillamine is composed of two main molecules, which are linked together to form its complex chemical structure.

Explanation

Bucillamine has been studied for its potential to reduce inflammation, oxidative stress, and modulate the immune system, making it a promising candidate for treating various medical conditions.

Explanation

The compound's potential therapeutic effects are attributed to its ability to reduce oxidative stress and inflammation, as well as enhance immune function, which could lead to improved outcomes in treating various diseases.

Type

Pharmaceutical compound

Composition

Carboxy-diphenyl-methyl disulfide and 2,2-diphenyl-acetic acid

Therapeutic effects

Anti-inflammatory, antioxidant, and immunomodulatory properties

Potential applications

Treatment of rheumatoid arthritis and COVID-19

Mechanism of action

Reducing oxidative stress, inflammation, and enhancing immune function

Upstream product

• 346578-06-1 2-[(2-oxo-1,1-diphenylethyl)disulfanyl]-2,2-diphenylethanal 
• 4695-15-2 2,2-diphenyl-2-mercaptoacetic acid 
• 947-91-1 Diphenylacetaldehyde 
• 18648-56-1 2-((Ξ)-α'-oxo-bibenzyl-α-ylidene)-5,5-diphenyl-[1,3]dithiolan-4-one 

Downstream Products

• 33177-40-1 2,2,2',2'-tetraphenyl-2,2'-disulfanediyl-di-acetic acid dimethyl ester 
• 1450-31-3 Thiobenzophenon 

Relevant articles and documents

First examples of oxidizing aldehydes to carboxylic acids in the presence of a tertiary disulfide functional group: Synthesis of novel diacid-disulfides

The disulfide functionality exists in numerous organic compounds of interest in both chemistry and biology. In view of the fact that the disulfide function is highly susceptible to further oxidation by a broad range of agents, conducting a chemoselective