193693-60-6 Usage
Uses
Fmoc-L-beta-homoproline is used as an important organic intermediate in the fields of agrochemicals, pharmaceuticals, and dyestuff. Its application in these industries is primarily due to its ability to enhance the properties and performance of the final products.
Used in Pharmaceutical Industry:
Fmoc-L-beta-homoproline is used as a building block in peptide synthesis, allowing for the creation of complex and specific peptide sequences. This is crucial for the development of new drugs and therapeutic agents, as peptides can be tailored to target specific biological pathways and receptors.
Used in Drug Screening:
In the drug screening process, Fmoc-L-beta-homoproline is utilized to create a diverse library of peptide-based compounds. These compounds can then be screened for potential biological activity, leading to the discovery of new drug candidates with specific therapeutic properties.
Used in Agrochemical Industry:
Fmoc-L-beta-homoproline is employed as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its incorporation can improve the effectiveness and selectivity of these chemicals, leading to more efficient and environmentally friendly products.
Used in Dyestuff Industry:
In the dyestuff industry, Fmoc-L-beta-homoproline is used to synthesize novel dyes with unique color properties and improved stability. This allows for the development of new and innovative colorants for various applications, such as textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 193693-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,9 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 193693-60:
(8*1)+(7*9)+(6*3)+(5*6)+(4*9)+(3*3)+(2*6)+(1*0)=176
176 % 10 = 6
So 193693-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO4/c23-20(24)12-14-6-5-11-22(14)21(25)26-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-4,7-10,14,19H,5-6,11-13H2,(H,23,24)/t14-/m0/s1
193693-60-6Relevant articles and documents
Synthesis of N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-Protected (Fmoc) β-Amino Acids (= Homo-α-Amino Acids) by Direct Homologation
Ellmerer-Mueller, Ernst P.,Broessner, Dagmar,Maslouh, Najib,Tako, Andreas
, p. 59 - 65 (1998)
The successful application of the Arndt-Eistert protocol starting from commercially available N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-protected (Fmoc) α-amino acids leading to enantiomerically pure N-Fmoc-Protected β-amino acids in only two steps and with high yield is reported.
Convenient and simple synthesis of N-{[(9H-fluoren-9- yl)methoxy]carbonyl}-(Fmoc) protected β-amino acids (=homo-α-amino acids) employing Fmoc-α-amino acids and dicyclohexylcarbodiimide(DCC) mixtures
Ananda,Suresh Babu
, p. 418 - 423 (2007/10/03)
A simple approach for the homologation of α-amino acids to β-amino acids by the Arndt-Eistert method employing Fmoc-α-amino acid and N, N1- dicyclohexylcarbodiimide (DCC) mixture for the acylation of diazomethane, synthesizing the key intermediates Fmoc-α-amino acyldiazomethanes as crystalline solids is described.
