Interesting facts
              Exploring Isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate
Isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate is a fascinating compound that showcases the intricate relationships between structure, function, and versatility in the realm of organic chemistry. Here are some intriguing aspects to consider:
- Biodiversity and Applications: This compound represents a unique blend of a thiazole ring and a benzimidazole moiety, which are prominent in many biological systems. Compounds with similar structures often exhibit antimicrobial and anticancer properties, making them subjects of significant research.
- Pharmacological Potential: The underlying mechanisms of compounds like isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate are of particular interest in medicinal chemistry. Researchers explore their potential as therapeutic agents, especially in targeting specific enzymes or receptors in disease pathways.
- Research Developments: Ongoing studies often involve the exploration of this compound's derivatives, which can lead to improved efficacy or reduced side effects in pharmacotherapy. The ability to modulate chemical properties through tiny structural changes is a key principle in drug development.
- Synthesis and Challenges: The synthesis of thiazole and benzimidazole derivatives can be complex, often requiring multi-step reactions. Overcoming challenges during synthesis is a captivating aspect of research, driving innovation and development in synthetic methodologies.
The intricate design of isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate not only emphasizes the beauty of chemical compounds but also highlights the vast potential they hold in the scientific community. As researchers continue to probe its unique properties, this compound remains a promising candidate for future discoveries in medicinal chemistry.
Synonyms
          Cambendazole
          26097-80-3
          Cambendazol
          Camvet
          Camdan
          Cambendazolum
          NSC-377071
          DTXSID0046852
          Isopropyl 2-(4-triazolyl)-5-benzimidazolecarbamate
          079X63S3DU
          Carbamic acid, (2-(4-thiazolyl)-1H-benzimidazol-5-yl)-, 1-methylethyl ester
          DTXCID8026852
          Carbamic acid, [2-(4-thiazolyl)-1H-benzimidazol-5-yl]-, 1-methylethyl ester
          RefChem:917943
          5-Isopropoxycarbonylamino-2-(4-thiazoyl)benzimidazole
          propan-2-yl N-(2-(1,3-thiazol-4-yl)-1H-1,3-benzodiazol-5-yl)carbamate
          247-459-5
          Urokinase
          Novazole
          Noviben
          9039-53-6
          Cambenzole
          Bonlam
          Equiben
          CBDZ
          MK 905
          NSC 377071
          propan-2-yl N-[2-(1,3-thiazol-4-yl)-3H-benzimidazol-5-yl]carbamate
          Cambendazole (>90%)
          MFCD00864552
          Carbamic acid, N-[2-(4-thiazolyl)-1H-benzimidazol-6-yl]-, 1-methylethyl ester
          5-BENZIMIDAZOLECARBAMIC ACID, 2-(4-THIAZOLYL)-, ISOPROPYL ESTER
          NSC377071
          NCGC00181110-01
          N-(Thiazolyl-4)-2, benzimidazolyl-5, carbamate D'isopropyle
          Cambendazole 100 microg/mL in Acetonitrile
          NOE [French]
          2-(4-Thiazolyl)-5-Isopropoxycarbonylaminobenzimidazole
          isopropyl (2-(thiazol-4-yl)-1H-benzo[d]imidazol-5-yl)carbamate
          MK 905; NSC 377071; Novazole; Bonlam; Cambendazole; Cambenzole
          Urokinase from human urine
          Cambendazol [INN-Spanish]
          Cambendazolum [INN-Latin]
          Cambendazole [USAN:INN:BAN]
          EINECS 247-459-5
          BRN 0563292
          UNII-079X63S3DU
          Cambendazol?
          Camdan (TN)
          CAMBENDAZOLE [MI]
          N-(Thiazolyl-4)-2, benzimidazolyl-5, carbamate d'isopropyle [French]
          Urolinase from human urine
          Cambendazole (USAN/INN)
          CAMBENDAZOLE [INN]
          CAMBENDAZOLE [USAN]
          SCHEMBL44000
          CAMBENDAZOLE [MART.]
          Isopropyl 2-(4-thiazolyl)-5-benzimidazolecarbamate
          MLS004712049
          CAMBENDAZOLE [WHO-DD]
          CHEMBL290578
          orb1304281
          SCHEMBL2895694
          SCHEMBL29409263
          CAMBENDAZOLE [GREEN BOOK]
          EX-A752
          MSK5515
          BCP07866
          Cambendazol; Cambendazole; Novazole
          Tox21_112724
          AKOS037515510
          DB11380
          NCGC00181110-02
          AC-33587
          DA-33500
          SMR003475014
          TS-08767
          CAS-26097-80-3
          HY-107483
          CS-0028606
          NS00009532
          D03340
          Cambendazole, VETRANAL(TM), analytical standard
          F554509
          5-Isopropoxycarbonylamino-2-(4-thiazolyl)benzimidazole
          Q15726127
          isopropyl N-(2-thiazol-4-yl-1H-benzimidazol-5-yl)carbamate
          isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate
          Isopropyl 2-(1,3-thiazol-4-yl)-1H-benzimidazol-5-ylcarbamate #
          (Methylethyloxy)-N-(2-(1,3-thiazol-4-yl)benzimidazol-5-yl)methanamide
          propan-2-yl N-[2-(1,3-thiazol-4-yl)-1H-1,3-benzodiazol-6-yl]carbamate
              
Solubility of isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate
The solubility of isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate is influenced by several factors. This compound exhibits varying solubility profiles based on the solvent used.
Key Points about its Solubility:
In summary, the solubility of isopropyl N-(2-thiazol-4-yl-3H-benzimidazol-5-yl)carbamate can be effectively maximized by using appropriate solvents and adjusting environmental conditions, demonstrating the critical role that these factors play in the compound's behavior in solution.