• 1. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
• 2. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
• 3. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 4. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 5. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147

Comprehensive Overview of tert-butyl N-[trans-3-aminocyclohexyl]carbamate (CAS No. 609788-04-7)

tert-butyl N-[trans-3-aminocyclohexyl]carbamate (CAS No. 609788-04-7) is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. This carbamate derivative is particularly valued for its role as a protecting group in peptide synthesis and as a versatile intermediate in the development of bioactive molecules. Its unique trans-3-aminocyclohexyl structure contributes to its stability and reactivity, making it a preferred choice for chemists and researchers.

In recent years, the demand for tert-butyl N-[trans-3-aminocyclohexyl]carbamate has surged due to its applications in drug discovery and medicinal chemistry. Researchers are increasingly exploring its potential in designing small molecule inhibitors and enzyme modulators, aligning with the growing interest in personalized medicine and targeted therapies. The compound's CAS No. 609788-04-7 is frequently searched in scientific databases, reflecting its relevance in cutting-edge research.

One of the key advantages of tert-butyl N-[trans-3-aminocyclohexyl]carbamate is its compatibility with solid-phase peptide synthesis (SPPS). This method is pivotal in producing peptides for therapeutic use, such as anticancer agents and antiviral drugs. The compound's tert-butyloxycarbonyl (Boc) group ensures efficient protection of amine functionalities, a critical step in multi-step synthetic routes. This feature has made it a staple in laboratories focusing on peptide-based therapeutics.

From an industrial perspective, tert-butyl N-[trans-3-aminocyclohexyl]carbamate is synthesized through optimized routes to ensure high purity and yield. Manufacturers emphasize green chemistry principles, such as reducing solvent waste and improving atom economy, to meet the increasing demand for sustainable chemical processes. These practices resonate with the global push toward environmentally friendly synthesis, a topic gaining traction in academic and industrial circles.

The compound's trans-3-aminocyclohexyl moiety also opens doors to applications in asymmetric catalysis and chiral auxiliaries. Its rigid cyclohexane backbone provides stereochemical control, which is essential for producing enantiomerically pure compounds. This aligns with the pharmaceutical industry's focus on chiral drugs, which often exhibit superior efficacy and safety profiles compared to their racemic counterparts.

In summary, tert-butyl N-[trans-3-aminocyclohexyl]carbamate (CAS No. 609788-04-7) is a multifaceted compound with significant implications in modern chemistry and drug development. Its role as a protecting group, synthetic intermediate, and chiral building block underscores its importance in both academic and industrial settings. As research continues to evolve, this compound is poised to remain a cornerstone in the advancement of bioactive molecule design and therapeutic innovation.

• 51857-17-1(NH2-C6-NH-Boc)
• 151476-40-3(tert-butyl N-(adamantan-1-yl)carbamate)
• 167081-25-6(tert-butyl N-[cis-4-hydroxycyclohexyl]carbamate)
• 132234-69-6(tert-butyl N-[endo-8-azabicyclo[3.2.1]octan-3-yl]carbamate)
• 111300-06-2(trans-4-(boc-amino)cyclohexanol)
• 73874-95-0(4-Boc-Aminopiperidine)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)