24277-38-1 Usage
Description
(S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate is a complex organic compound with a specific stereochemistry (S)-configuration. It is characterized by its unique molecular structure, which includes a tert-butyl group, a methyl group, and a (tert-butoxycarbonyl)amino group attached to a pentanedioate backbone. (S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate is typically utilized as an intermediate in the synthesis of various pharmaceuticals and bioactive molecules due to its versatile functional groups and specific stereochemistry.
Uses
Used in Pharmaceutical Synthesis:
(S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate is used as an intermediate in the synthesis of Isodesmosine Chloride Hydrate (Synthetic) (I815051), which is a component of elastin. (S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate plays a crucial role in the development of new drugs targeting elastin-related diseases and conditions.
Used in Material Science:
In the field of material science, (S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate can be used as a building block for the development of novel polymers and materials with specific properties. Its unique structure and functional groups allow for the creation of materials with tailored characteristics, such as improved mechanical strength, flexibility, or responsiveness to environmental stimuli.
Used in Chemical Research:
As a complex organic molecule with a specific stereochemistry, (S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate is also valuable in chemical research. It can be employed as a model compound to study various aspects of organic chemistry, such as stereoselective reactions, conformational analysis, and the investigation of molecular interactions with other molecules or biological targets.
Used in Drug Delivery Systems:
Similar to gallotannin, (S)-1-tert-Butyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate can potentially be incorporated into drug delivery systems to improve the bioavailability and therapeutic outcomes of associated pharmaceuticals. Its unique structure and functional groups may allow for the development of targeted drug delivery systems, enhancing the efficacy and specificity of drug treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 24277-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,7 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24277-38:
(7*2)+(6*4)+(5*2)+(4*7)+(3*7)+(2*3)+(1*8)=111
111 % 10 = 1
So 24277-38-1 is a valid CAS Registry Number.
24277-38-1Relevant articles and documents
A study of polychlorinated leucine derivatives: Synthesis of (2S,4S)-5,5-dichloroleucine
Ardá, Ana,Jiménez, Carlos,Rodríguez, Jaime
, p. 3241 - 3243 (2007/10/03)
The first total synthesis of (2S,4S)-5,5-dichloroleucine has been achieved in 11 steps from L-pyroglutamic acid. A key step is the dichlorination process on the hydrazone of aldehyde 13 with CuCl2 in triethylamine.
