37618-00-1

Usage

Uses

Used in Pharmaceutical Industry:
Gossypol is utilized as a pharmaceutical agent for its potential anti-cancer properties, targeting a variety of cancer types. Its mechanism of action involves the inhibition of cancer cell growth, making it a candidate for further research and development in oncology.
Used in Fertility Regulation:
In the area of fertility regulation, Gossypol serves as an anti-fertility agent, with potential applications in contraceptive development. Its ability to impact fertility makes it a subject of interest for reproductive health research.
Used in Anti-microbial Applications:
Within the anti-microbial sector, Gossypol is employed for its potential to combat microbial infections. Its anti-microbial properties position it as a candidate for use in treatments aimed at reducing the spread of infectious diseases.
Used in Anti-inflammatory Treatments:
Gossypol is also considered for use in anti-inflammatory treatments, given some research suggesting it may possess anti-inflammatory effects. This potential use highlights its versatility in the medical field, offering possibilities for managing inflammation-related conditions.

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 119-67-5 o-carboxybenzaldehyde 
• 16859-59-9 3-hydroxy-1(3H)-isobenzofuranone 
• 1829-28-3 ethyl 2-iodobenzoate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 35849-09-3 o-bromobenzaldehyde dimethyl acetal 
• 114574-44-6 2-(3,4-dimethoxy-α-hydroxybenzyl)benzaldehyde dimethylacetal 
• 88-65-3 2-bromobenzoic-acid 

Downstream Products

• 51439-85-1 2-(3,4-dimethoxybenzoyl)benzoic acid 
• 856118-64-4 1-(3,4-dimethoxyphenyl)-3-(thiophen-2-yl)benzo[c]thiophene 
• 188559-96-8 4-(3,4-Dimethoxy-phenyl)-9-hydroxy-3H-naphtho[2,3-c]furan-1-one 
• 1401614-38-7 C₂₀H₁₆O₃S 
• 1401613-21-5 4-(3,4-dimethoxyphenyl)naphtho[2,3-b]thiophene 
• 1401613-60-2 C₃₀H₃₆O₆S 
• 1401614-08-1 2-(3,4-dimethoxybenzoyl)phenyl(thiophene-2-yl)methanone 
• 1401613-30-6 9-(3,4-dimethoxyylphenyl)-2-methylanthracene 
• 1401613-71-5 C₃₃H₄₀O₆ 
• 1401614-14-9 2-(3,4-dimethoxybenzoyl)phenyl(p-tolyl)methanone 

Relevant academic research and scientific papers

Synthesis and characterization of benzannelated thienyl oligomers

An array of 1,3-diarylbenzo[c]thiophenes have been synthesized by the ring-opening of lactones followed by thionation using Lawesson's reagent with concurrent intramolecular cyclization. Photophysical studies of the various benzo[c]thiophene analogues are presented. The results of a cyclic voltammetric investigation of the benzo[c]thiophenes are also reported.

Synthesis of 1,3-diaryl benzo[c]thiophenes

An array of 1,3-diarylbenzo[c]thiophenes has been synthesized via the ring opening of lactones followed by thionation using Lawesson's reagent.

Efficient Synthesis of 3-Arylphthalides

A convenient method for the synthesis of 3-arylphthalodes (3a-q) involving condensation of phthalaldehydric acids (1a,b) with aromatic substrates (2a-k) in the presence of TFA is described.

A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans

The 9-aryl-4-oxynaphthofuran-1(3H)-one system is generally synthesized in two steps from α-aryl-o-toluic acid derivatives. The method involves a tandem conjugate addition-Dieckmann type condensation between α-lithiated α-aryl-o-toluic acid derivatives and

Indane-1,3-dione, Phthalimidine and Phthalide Derivatives as Alkylating Agents

The title compounds gave carbocations in acid media.The electrophilic aromatic substitution of those carbocations was studied.