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2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is a complex chemical compound that is part of the isoquinolinone derivatives class. It is characterized by its white solid appearance and a molecular formula of C21H17NO. 2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is widely recognized for its potential biological activities and is extensively utilized in research and pharmaceutical applications. Its therapeutic properties are currently under investigation, with a focus on its potential as an enzyme and receptor inhibitor, as well as its possible applications in treating various medical conditions such as cancer, neurological disorders, and inflammation.

21868-93-9

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21868-93-9 Usage

Uses

Used in Pharmaceutical Research:
2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is used as a research compound for its potential biological activities, particularly in the development of new drugs. It is being studied for its ability to inhibit various enzymes and receptors, which could lead to the creation of novel therapeutic agents.
Used in Cancer Treatment:
In the field of oncology, 2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is being explored as a potential anticancer agent. Its application is based on the compound's ability to interact with cellular targets, which may inhibit tumor growth and progression.
Used in Neurological Disorders:
2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is also being investigated for its potential role in the treatment of neurological disorders. 2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one's interaction with specific receptors and enzymes could offer new avenues for managing conditions such as Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders.
Used in Inflammation Management:
In the context of inflammation, 2,3-diphenyl-3,4-dihydroisoquinolin-1(2H)-one is being studied for its potential to modulate the immune response and reduce inflammation. This could lead to new treatments for conditions such as arthritis, autoimmune diseases, and other inflammatory disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 21868-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21868-93:
(7*2)+(6*1)+(5*8)+(4*6)+(3*8)+(2*9)+(1*3)=129
129 % 10 = 9
So 21868-93-9 is a valid CAS Registry Number.

21868-93-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-3,4-dihydro-2H-benzo[1,4]thiazine

1.2 Other means of identification

Product number -
Other names 2,3-Diphenyl-3,4-dihydro-isocarbostyril

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21868-93-9 SDS

21868-93-9Downstream Products

21868-93-9Relevant academic research and scientific papers

Intramolecular Hydroamidation of ortho-Vinyl Benzamides Promoted by Potassium tert-Butoxide/N,N-Dimethylformamide

Chen, Zhen-Yu,Wu, Liang-Yu,Fang, Hai-Sheng,Zhang, Ting,Mao, Zhi-Feng,Zou, Yong,Zhang, Xue-Jing,Yan, Ming

supporting information, p. 3894 - 3899 (2017/10/07)

An intramolecular hydroamidation of ortho-vinyl benzamides had been developed. The reaction was promoted efficiently by potassium tert-butoxide and N,N-dimethylformamide without the need for strong oxidants or transition-metal catalysts. A series of dihyd

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