61532-58-9 Usage
Chemical class
Benzimidazole
The compound belongs to the benzimidazole class, which is a group of heterocyclic compounds known for their various biological activities and potential applications.
Heterocyclic compound
Contains both benzimidazole and oxazolo rings
The compound is characterized by the presence of two heterocyclic rings, which contribute to its structural diversity and potential biological activity.
Morpholine group
Attached to the benzimidazole ring
The presence of a morpholine group in the compound provides unique properties, such as stability and the ability to form hydrogen bonds, which can be advantageous in drug design.
Potential applications
Pharmaceutical and agrochemical industries
Due to its unique properties and structural features, 2-(morpholin-4-ylmethyl)-2,3-dihydro[1,3]oxazolo[3,2-a]benzimidazole may have potential applications in the pharmaceutical and agrochemical industries.
Drug candidate
Potential for further research and development
The compound's structural diversity and potential biological activity make it a promising candidate for further research and development as a potential drug.
Check Digit Verification of cas no
The CAS Registry Mumber 61532-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,3 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61532-58:
(7*6)+(6*1)+(5*5)+(4*3)+(3*2)+(2*5)+(1*8)=109
109 % 10 = 9
So 61532-58-9 is a valid CAS Registry Number.
61532-58-9Relevant articles and documents
The -NH-(C=)-Br functionality of heteroaromatic compounds as a synthon for fused dihydrooxazoles
Cegla, Marek T.,Baran, Marzena,Czarny, Agnieszka,Zylewski, Marek,Potaczek, Joanna,Klenc, Jeff,Strekowski, Lucjan
experimental part, p. 720 - 723 (2011/07/31)
Fused dihydrooxazoles are produced by the reaction of 8-bromoteophylline (1), 6-bromo-2-pyridone (7), or 2-bromobenzimidazole (11) with an N-substituted N-(2,3-epoxypropyl)amine. The product derived from 1 undergoes rearrangement to a fused dihydrooxazine
