• 1. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210
• 2. An atom efficient route to N-aryl and N-alkyl pyrrolines by transition metal catalysis?
  Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
• 3. An insight into the role of side chains in the microstructure and carrier mobility of high-performance conjugated polymers?
  Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
• 4. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
• 5. Alumina grafted SBA-15 sustainable bifunctional catalysts for direct cross-coupling of benzylic alcohols to diarylmethanes?
  Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Diazinanes Piperazines N-alkylpiperazines

Compound CAS No. 114086-15-6: 2-Methyl-2,5-Diazabicyclo[2.2.1]Heptane; Dihydrobromide

The compound with CAS No. 114086-15-6, commonly referred to as 2-methyl-2,5-diazabicyclo[2.2.1]heptane; dihydrobromide, is a significant molecule in the field of organic chemistry and pharmacology. This compound belongs to the class of bicyclic amines, which are known for their unique structural properties and diverse applications in drug design and synthesis.

Bicyclic amines like 2-methyl-2,5-diazabicyclo[2.2.1]heptane have gained attention due to their ability to form stable structures that can mimic natural bioactive molecules. The dihydrobromide salt of this compound is particularly notable for its role in various chemical reactions and its potential in medicinal chemistry.

Recent studies have highlighted the importance of bicyclic amines in the development of novel therapeutic agents. For instance, researchers have explored the use of 2-methyl-2,5-diazabicyclo[2.2.1]heptane; dihydrobromide as a precursor in the synthesis of bioactive compounds with potential anti-inflammatory and analgesic properties. These findings underscore the compound's versatility and its growing relevance in modern drug discovery.

The synthesis of CAS No. 114086-15-6 involves a multi-step process that typically includes ring-closing reactions and subsequent bromination to form the dihydrobromide salt. The structural integrity of this compound is crucial for its stability and reactivity, making it an ideal candidate for further functionalization in organic synthesis.

Moreover, advancements in computational chemistry have enabled researchers to predict the pharmacokinetic properties of 2-methyl-2,5-diazabicyclo[2.2.1]heptane; dihydrobromide with greater accuracy. These computational models have provided insights into the compound's absorption, distribution, metabolism, and excretion (ADME) profiles, paving the way for its potential use in pharmaceutical formulations.

In conclusion, CAS No. 114086-15-6, or 2-methyl-2,5-diazabicyclo[2.2.1]heptane; dihydrobromide, represents a promising molecule with wide-ranging applications in organic synthesis and drug development. Its unique structural features and favorable chemical properties make it a valuable asset in contemporary research.

• 125224-64-8((1R,4R)-2-methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide)
• 127420-27-3((1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrochloride)
• 845866-61-7(2-ethyl-2,5-diazabicyclo[2.2.1]heptane)
• 125224-62-6((1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide)
• 134679-22-4((1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane)
• 444664-95-3(2-Isopropyl-2,5-diazabicyclo[2.2.1]heptane)
• 59436-24-7(Pyrrolo[1,2-a]pyrazine-2(1H)-propanamine, hexahydro- (9CI))
• 460365-24-6(2,5-Diazabicyclo[2.2.1]heptane,2-cyclohexyl-(9CI))
• 59436-77-0(2-Methyl-2,5-diazabicyclo[2.2.1]heptane)
• 767291-68-9(2,5-Diazabicyclo[2.2.1]heptane,2,5-dimethyl-,(1S,4S)-(9CI))