93623-54-2

Upstream product

• 95-68-1 2,4-Xylidine 
• 39842-01-8 2,4-dimethylphenylisothiocyanate 
• 463-71-8 thiophosgene 
• 75-15-0 carbon disulfide 

Downstream Products

• 21789-36-6 2,4-dimethylbenzonitrile 
• 39842-01-8 2,4-dimethylphenylisothiocyanate 
• 97-37-0 N,N'-di-(2,4-dimethyl-phenyl)-guanidine 
• 1017535-51-1 1-acetyl-1,3-di-(o,p-dimethylphenyl)urea 
• 1158080-98-8 C₁₈H₁₈N₂OS 
• 63520-50-3 1,3-bis(2,4-dimethylphenyl)carbodiimide 
• 1158081-04-9 C₁₈H₂₀N₄O 
• 1011794-21-0 3-(2',4'-dimethylphenyl)-2-(2',4'-dimethylphenylimino)-4-methyl-3H-thiazole 
• 13278-55-2 N-(2,4-dimethyl-phenyl)-N'-methyl-thiourea 

Relevant academic research and scientific papers

Novel non-peptidic small molecule inhibitors of secreted aspartic protease 2 (SAP2) for the treatment of resistant fungal infections

Targeting secreted aspartic protease 2 (SAP2), a kind of virulence factor, represents a new strategy for antifungal drug discovery. In this report, the first-generation of small molecule SAP2 inhibitors was rationally designed and optimized using a structure-based approach. In particular, inhibitor 23h was highly potent and selective and showed good antifungal potency for the treatment of resistant Candida albicans infections.

A facile method for the preparation of carbodiimides from thioureas and (Boc)2O

A concise method for the preparation of carbodiimides from thioureas using di-tert-butyl dicarbonate [(Boc)2O] as the dehydrosulfurizative reagent has been developed. Using DMAP as the catalyst, a variety of symmetric and asymmetric 1,3-diaryl thioureas were converted into the corresponding carbodiimides efficiently in a short time.

Synthesis and conformational features of sym N,N′,N″- triarylguanidines

A one pot reaction involving sym N,N′-diarylthiourea and the respective arylamine in the presence of aq. KOH in nitrobenzene at ≥105°C afforded sym N,N′,N″-triarylguanidine in fair to good yield and the products have been characterized. Sym N,N′,N″-tri(4-tolyl)guanidine possesses (7) anti-anti conformation, sym N,N′,N″-tri(2-tolyl) guanidine (8) and sym N,N′,N″-tris(2,4-xylyl)guanidine (11) each possess anti-anti αβα conformation whereas sym N,N′,N″-tris(2-anisyl)guanidine possesses (9) syn-anti αββ conformation as determined by single crystal X-ray diffraction data. The observed conformations appear to result from a subtle balance between steric factor associated with the aryl substituent and multiple electronic factors namely n-π conjugation/negative hyperconjugation and non-covalent interactions in the crystal lattice. Indian Academy of Sciences.