71869-43-7 Usage
Uses
Used in Pharmaceutical Research:
Cyclopentanecarboxylic acid, 3-amino-, (1R,3R)(9CI) is used as a building block for the synthesis of biologically active compounds in pharmaceutical research. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Drug Synthesis:
In the pharmaceutical industry, Cyclopentanecarboxylic acid, 3-amino-, (1R,3R)(9CI) is used as a key intermediate in the synthesis of various drugs. Its versatility and reactivity in chemical reactions allow for the creation of a wide range of pharmaceutical compounds with potential therapeutic applications.
Used in Chiral Chemistry:
Cyclopentanecarboxylic acid, 3-amino-, (1R,3R)(9CI) is also used in chiral chemistry, where its specific enantiomeric form is crucial for the development of enantiomerically pure compounds. This is particularly important in the pharmaceutical industry, as the biological activity and safety of chiral drugs can be significantly influenced by their stereochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 71869-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71869-43:
(7*7)+(6*1)+(5*8)+(4*6)+(3*9)+(2*4)+(1*3)=157
157 % 10 = 7
So 71869-43-7 is a valid CAS Registry Number.
71869-43-7Relevant academic research and scientific papers
Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar αvβ3/ αvβ5 integrin dual binders
Casiraghi, Giovanni,Rassu, Gloria,Auzzas, Luciana,Burreddu, Paola,Gaetani, Enrico,Battistini, Lucia,Zanardi, Franca,Curti, Claudio,Nicastro, Giuseppe,Belvisi, Laura,Motto, Ilaria,Castorina, Massimo,Giannini, Giuseppe,Pisano, Claudio
, p. 7675 - 7687 (2007/10/03)
Eleven γ-aminocyclopentane carboxylic acid (Acpca) platforms, including four dihydroxy representatives (19-22), three hydroxy analogues (34-36), and four deoxy derivatives (30-33), were prepared in a chiral nonracemic format. These simple units were then
