524674-38-2 Usage
HCl salt form
It is the HCl salt form of the benzimidazole derivative.
Pharmaceutical use
It is commonly used in various pharmaceutical formulations and research studies.
Potential pharmacological properties
It has potential pharmacological properties.
Interaction with receptors
It is known for its ability to interact with specific receptors in the central nervous system.
Potential therapeutic effects
The interaction with specific receptors in the central nervous system may contribute to its potential therapeutic effects.
Unique chemical structure
It has a unique chemical structure.
Drug development
Its unique chemical structure makes it a valuable component in the development of new drugs for the treatment of various medical conditions.
Applications in pharmacology and medicine
It has potential applications in the field of pharmacology and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 524674-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,6,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 524674-38:
(8*5)+(7*2)+(6*4)+(5*6)+(4*7)+(3*4)+(2*3)+(1*8)=162
162 % 10 = 2
So 524674-38-2 is a valid CAS Registry Number.
524674-38-2Relevant academic research and scientific papers
Ligand regulation for manganese-catalyzed enantioselective epoxidation of olefins without acid
Xu, Daqian,Sun, Qiangsheng,Lin, Jin,Sun, Wei
, p. 13101 - 13104 (2020/11/09)
A novel manganese catalyst bearing an l-proline-derived N4 ligand has been developed for enabling acid-free asymmetric epoxidation of olefins with tert-butyl hydroperoxide as the oxidant. A variety of olefins that are well-matched in size with the ligand
The synthesis of chiral tridentate ligands from L-proline and their application in the copper(II)-catalyzed enantioselective Henry reaction
Xu, Daqian,Sun, Qiangsheng,Quan, Zhengjun,Sun, Wei,Wang, Xicun
, p. 954 - 963 (2017/07/11)
A series of chiral tridentate ligands derived from readily available enantiopure L-proline were designed and synthesized. The ligands together with Cu(OAc)2 were successfully used in asymmetric Henry reactions. Various structurally divergent aldehydes and nitromethane were converted into versatile β-nitro alcohols in MeOH at room temperature with very good yields (up to 85%) and enantioselectivities (up to 86%).
