104682-00-0 Usage
Description
(1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid is a complex and specific chemical compound with a cyclopropane carboxylic acid backbone. It features a tert-butoxycarbonyl-protected amino group and a methoxycarbonylmethyl group, and its stereochemistry is precisely defined, which is crucial for its potential applications. (1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid may have unique properties due to its intricate structure, making it a promising candidate for various uses in fields such as organic synthesis and medicinal chemistry.
Uses
Used in Organic Synthesis:
(1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid is used as a key intermediate in organic synthesis for the creation of complex molecules. Its unique functional groups and stereochemistry allow for specific reactions that can lead to the formation of novel compounds with potential applications in various industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid is used as a building block for the development of new pharmaceuticals. Its specific stereochemistry and functional groups can be leveraged to design drugs with improved efficacy and selectivity, targeting various diseases and medical conditions.
Used in Pharmaceutical Development:
(1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid is utilized in pharmaceutical development as a precursor for the synthesis of potential drug candidates. Its unique structure and properties can contribute to the discovery of new therapeutic agents with specific mechanisms of action, offering innovative treatment options for patients.
Used in Research and Development:
In research and development settings, (1R,2S)-2-((S)-tert-Butoxycarbonylamino-methoxycarbonyl-methyl)-cyclopropanecarboxylic acid serves as a valuable tool for studying the effects of stereochemistry on molecular interactions and biological activity. Its complex nature allows scientists to explore new avenues in chemical and biological research, potentially leading to breakthroughs in various scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 104682-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104682-00:
(8*1)+(7*0)+(6*4)+(5*6)+(4*8)+(3*2)+(2*0)+(1*0)=100
100 % 10 = 0
So 104682-00-0 is a valid CAS Registry Number.