175136-52-4 Usage
Chemical structure
An oxime derivative of 1H-benzo[d]imidazole, which is an organic compound containing a benzene ring fused with an imidazole ring and a phenyl group.
Therapeutic potential
The compound has potential therapeutic properties and is being studied for its possible use in treating various inflammatory and autoimmune conditions, as well as for its potential neuroprotective effects.
Anti-inflammatory activity
The compound is known for its ability to reduce inflammation, which may be beneficial in treating conditions such as rheumatoid arthritis and cardiovascular disorders.
Antioxidant activity
The compound exhibits antioxidant properties, which may help protect cells from damage caused by free radicals and oxidative stress, potentially slowing down the progression of neurodegenerative diseases.
Potential applications
The compound is being researched for its potential use in treating a range of conditions, including rheumatoid arthritis, neurodegenerative diseases (e.g., Alzheimer's, Parkinson's), and cardiovascular disorders.
Ongoing research
Further studies are being conducted to explore the full range of therapeutic applications for this compound and to determine its safety and efficacy in clinical settings.
Check Digit Verification of cas no
The CAS Registry Mumber 175136-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175136-52:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*5)+(1*2)=134
134 % 10 = 4
So 175136-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N3O2/c17-15-10-7-4-8-11-12(10)14-13(16(11)18)9-5-2-1-3-6-9/h1-3,5-6,17-18H,4,7-8H2/b15-10-
175136-52-4Relevant articles and documents
Synthesis of 1,5,6,7-tetrahydro-4H-benzimidazol-4-one derivatives from 2,6-bis(hydroxyimino)cyclohexan-1-one
Samsonov
, p. 66 - 73 (2017/03/16)
The reaction of 2,6-bis(hydroxyimino)cyclohexan-1-one with aldehydes and ammonia afforded 2-substituted 4-hydroxyimino-4,5,6,7-tetrahydro-1H-benzimidazol-1-ols which were hydrolyzed to 1-hydroxy- 2-R-1,5,6,7-tetrahydro-4H-benzimidazol-4-ones. The N-hydroxy group in the latter can readily by removed by the action of chloroacetone in the presence of a base (potassium carbonate or triethylamine); as a result, 2-substituted 1,5,6,7-tetrahydro-4H-benzimidazol-4-ones were obtained.
