270263-04-2 Usage
Uses
Used in Organic Synthesis:
FMOC-(S)-3-AMINO-5-HEXENOIC ACID is used as a building block in organic synthesis for the preparation of complex organic molecules, leveraging its unique structural features to facilitate the formation of desired chemical entities.
Used in Peptide and Peptidomimetic Synthesis:
In the field of peptide chemistry, FMOC-(S)-3-AMINO-5-HEXENOIC ACID is used as a component in the synthesis of peptides and peptidomimetics. Its incorporation allows for the creation of bioactive molecules with specific properties, such as enhanced stability or selectivity towards biological targets.
Used in Medicinal Chemistry:
FMOC-(S)-3-AMINO-5-HEXENOIC ACID is utilized in medicinal chemistry as a tool for the development of new drugs. Its ability to modify peptide properties makes it a valuable asset in the design of therapeutic agents with improved pharmacokinetics and pharmacodynamics.
Used in Drug Development:
In the pharmaceutical industry, FMOC-(S)-3-AMINO-5-HEXENOIC ACID is used as a key component in drug development. Its role in the synthesis of bioactive peptides and peptidomimetics contributes to the discovery of novel therapeutic agents with potential applications in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 270263-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,6 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 270263-04:
(8*2)+(7*7)+(6*0)+(5*2)+(4*6)+(3*3)+(2*0)+(1*4)=112
112 % 10 = 2
So 270263-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO4/c1-2-7-14(12-20(23)24)22-21(25)26-13-19-17-10-5-3-8-15(17)16-9-4-6-11-18(16)19/h2-6,8-11,14,19H,1,7,12-13H2,(H,22,25)(H,23,24)/t14-/m0/s1
270263-04-2Relevant academic research and scientific papers
Synthesis of a natural product-inspired eight-membered ring lactam library via ring-closing metathesis
Brown, Neil,Xie, Baohan,Markina, Nataliya,VanderVelde, David,Perchellet, Jean-Pierre H.,Perchellet, Elisabeth M.,Crow, Kyle R.,Buszek, Keith R.
scheme or table, p. 4876 - 4879 (2009/05/30)
We have prepared a novel speculative eight-membered lactam demonstration library based on the skeletal structure of the potent antitumor marine natural product octalactin A. The basic scaffold was readily constructed in a convergent fashion via ring-closing metathesis chemistry from the corresponding diene amides. A cursory examination of the biological properties of the library validates the relevance and significance of these structures.
