93750-30-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-METHOXYPHENOXY)PROPYLAMINE is used as an intermediate in the synthesis of medications for its ability to contribute to the development of new pharmaceutical compounds.
Used in Agriculture:
2-(4-METHOXYPHENOXY)PROPYLAMINE is used as an intermediate in the production of agrochemicals, playing a role in the creation of substances that can enhance crop protection and yield.
Used in Material Science:
2-(4-METHOXYPHENOXY)PROPYLAMINE is used in the synthesis of polymers, contributing to the development of new materials with specific properties for various applications.
Used as a Research Reagent:
In chemical laboratories, 2-(4-METHOXYPHENOXY)PROPYLAMINE is used as a research reagent to support various scientific investigations, aiding in the advancement of chemical knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 93750-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93750-30:
(7*9)+(6*3)+(5*7)+(4*5)+(3*0)+(2*3)+(1*0)=142
142 % 10 = 2
So 93750-30-2 is a valid CAS Registry Number.
93750-30-2Relevant academic research and scientific papers
Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors
Carocci, Alessia,Catalano, Alessia,Lovece, Angelo,Lentini, Giovanni,Duranti, Andrea,Lucini, Valeria,Pannacci, Marilou,Scaglione, Francesco,Franchini, Carlo
experimental part, p. 6496 - 6511 (2010/10/02)
A series of phenoxyalkyl and phenylthioalkyl amides were prepared as melatoninergic ligands. Modulation of affinity of the newly synthesized compound by applying SARs around the terminal amide moiety, the alkyl chain, and the methoxy group on the aromatic ring provides compounds with nanomolar affinity for both melatonin receptor subtypes. Affinity towards MT1 and MT2 receptors were modulated also exploiting chirality. The investigation of intrinsic activity revealed that all the tested compounds behave as full or partial agonists.
