64191-13-5 Usage
General Description
(1S,2S)-(-)-2-Amino-1-cyclopentanecarboxylic acid is a chiral amino acid with a cyclopentane ring structure. It is a solid, white powder at room temperature and is a non-essential amino acid, meaning it can be synthesized by the body and does not need to be obtained from the diet. (1S,2S)-(-)-2-Amino-1-cyclopentanecarboxylic acid is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds. It also has potential applications in the field of medicinal chemistry and drug design, particularly for the development of new therapeutic agents. Additionally, it may also have uses in the field of biochemistry and as a research reagent in chemical and biological laboratories.
Check Digit Verification of cas no
The CAS Registry Mumber 64191-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64191-13:
(7*6)+(6*4)+(5*1)+(4*9)+(3*1)+(2*1)+(1*3)=115
115 % 10 = 5
So 64191-13-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c7-5-3-1-2-4(5)6(8)9/h4-5H,1-3,7H2,(H,8,9)/t4-,5-/m0/s1
64191-13-5Relevant articles and documents
Chiral ligand-controlled asymmetric conjugate amination of enoates with lithium mesitylmethyl(trimethylsilyl)amide
Sakai, Takeo,Doi, Hirohisa,Tomioka, Kiyoshi
, p. 8351 - 8359 (2007/10/03)
Lithium mesitylmethyl(trimethylsilyl)amide behaved as a nice amination agent in a chiral ligand-controlled conjugate addition reaction of tert-butyl cinnamate to give the conjugate amination product with 99% ee in 90% yield. Other acyclic and cyclic enoat
(S,S)-trans-cyclopentane-constrained peptide nucleic acids. A general backbone modification that improves binding affinity and sequence specificity
Pokorski, Jonathan K.,Witschi, Mark A.,Purnell, Bethany L.,Appella, Daniel H.
, p. 15067 - 15073 (2007/10/03)
Replacing the ethylenediamine portion of aminoethylglycine peptide nucleic acids (aegPNAs) with one or more (S,S)-trans-cyclopentane diamine units significantly increases binding affinity and sequence specificity to complementary DNA, making these modifie