210883-65-1 Usage
Uses
Used in Pharmaceutical Industry:
(L)-2-(9H-fluoren-9-ylmethoxycarbonyl)-3-octylsulfanyl-propionic acid is used as a protecting group in peptide synthesis for the Fmoc group, which is crucial in the development of new pharmaceuticals. Its role in peptide synthesis allows for the creation of complex peptide structures with potential therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, (L)-2-(9H-fluoren-9-ylmethoxycarbonyl)-3-octylsulfanyl-propionic acid is used as a building block for the synthesis of more complex molecules. Its unique structure and functional groups make it a valuable component in the design and synthesis of novel organic compounds with potential applications in various industries.
Used in Biochemical Research:
(L)-2-(9H-fluoren-9-ylmethoxycarbonyl)-3-octylsulfanyl-propionic acid is also utilized in biochemistry for studying the interactions between peptides and other biomolecules. (L)-2-(9H-fluoren-9-ylmethoxycarbonyl)-3-octylsulfanyl-propionic acid's properties may provide insights into the development of new bioactive molecules or the understanding of biological processes at the molecular level.
Check Digit Verification of cas no
The CAS Registry Mumber 210883-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,8,8 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210883-65:
(8*2)+(7*1)+(6*0)+(5*8)+(4*8)+(3*3)+(2*6)+(1*5)=121
121 % 10 = 1
So 210883-65-1 is a valid CAS Registry Number.
210883-65-1Relevant academic research and scientific papers
Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction
Triola, Gemma,Brunsveld, Luc,Waldmann, Herbert
, p. 3646 - 3649 (2008/09/20)
(Chemical Equation Presented) Treatment of differently protected and unprotected cysteines with a variety of alkenes in the presence of a radical initiator (AIBN) afforded the corresponding S-alkylated cysteines in high yields and without racemization.
