71869-43-7 Usage
General Description
Cyclopentanecarboxylic acid, 3-amino-, (1R,3R)- (9CI) is a chemical compound with the molecular formula C6H11NO2. It is an amino acid derivative, specifically an enantiomer of 3-aminocyclopentanecarboxylic acid. Cyclopentanecarboxylic acid, 3-amino-, (1R,3R)- (9CI) exists as a white crystalline solid and is commonly used in pharmaceutical research as a building block for the synthesis of various biologically active compounds. It is important to note that the (1R,3R)- designation indicates that this compound has two chiral centers, with the (1R,3R)-enantiomer being one of the possible stereoisomers. As with all amino acids, it plays an essential role in the structure and function of proteins within living organisms.
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 articles and documents
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
Synthesis of analogues of GABA. IV. Three unsaturated derivatives of 3-aminocyclopentane-1-carboxylic acid
Allan,Twitchin
, p. 599 - 604 (2007/10/02)
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