229323-07-3 Usage
General Description
(S)-3-aminomethyl-1-benzylpyrrolidine is a chemical compound that belongs to the class of pyrrolidine derivatives. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the (S)-enantiomer is the specific form being referred to in this case. (S)-3-AMINOMETHYL-1-BENZYLPYRROLIDINE has potential applications in medicinal chemistry and drug development, particularly in the synthesis of new pharmaceuticals. It can also be used as a building block in organic synthesis, enabling the creation of more complex compounds. Additionally, (S)-3-aminomethyl-1-benzylpyrrolidine may have potential biological activities and could be the subject of further research in the field of pharmacology and biochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 229323-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,3,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 229323-07:
(8*2)+(7*2)+(6*9)+(5*3)+(4*2)+(3*3)+(2*0)+(1*7)=123
123 % 10 = 3
So 229323-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2/c13-8-12-6-7-14(10-12)9-11-4-2-1-3-5-11/h1-5,12H,6-10,13H2/t12-/m0/s1
229323-07-3Relevant articles and documents
QUINOLONE ANTIBACTERIAL AGENTS
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Page/Page column 87; 88; 120, (2010/02/12)
Compounds of formula (I) wherein A is formula (II), formula (III) or formula (IV), and B is formula (V), formula (VI), or formula (VII), can be used in a variety of applications including use as antibacterial agents.
Enantio- and diastereocontrolled dopamine D1, D2, D3 and D4 receptor binding of N-(3-pyrrolidinylmethyl)benzamides synthesized from aspartic acid
Thomas, Christoph,Huebner, Harald,Gmeiner, Peter
, p. 841 - 846 (2007/10/03)
Subreceptor selectivity tuning of N-(3-pyrrolidinyl)benzamides leading to the selective dopamine D3 ligand ent1h and the derivatives 1g and 1e/ent1e which preferably recognize human D2 or D4 receptors, respectively, is described. Binding profiles were con
