124392-75-2 Usage
Uses
Used in Pharmaceutical Research:
2H-(1)Benzoxepino(5,4-c)pyrazole, 4,5-dihydro-9-methyl-3-(4-methylphenyl)-2-phenylis utilized as a subject of pharmaceutical research for its potential to contribute to the development of new drugs. Its unique molecular structure may offer novel interactions with biological targets, leading to the discovery of new therapeutic agents.
Used in Materials Science:
In the field of materials science, 2H-(1)Benzoxepino(5,4-c)pyrazole, 4,5-dihydro-9-methyl-3-(4-methylphenyl)-2-phenylmay serve as a building block for the synthesis of new materials with specialized properties. Its tricyclic nature and substituents could allow for the creation of materials with tailored characteristics for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 124392-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124392-75:
(8*1)+(7*2)+(6*4)+(5*3)+(4*9)+(3*2)+(2*7)+(1*5)=122
122 % 10 = 2
So 124392-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H22N2O/c1-17-8-11-19(12-9-17)25-21-14-15-28-23-13-10-18(2)16-22(23)24(21)26-27(25)20-6-4-3-5-7-20/h3-13,16H,14-15H2,1-2H3
124392-75-2Relevant articles and documents
Synthesis and Biological Activities of 8,9-Disubstituted 4,5-Dihydro-2H--benzoxepinopyrazoles and Related Compounds
Tripathi, Ravish C.,Tandon, V. K.,Khanna, J. M.,Saxena, Anil K.,Anand, Nitya
, p. 37 - 41 (2007/10/02)
Condensation of 2,3,4,5-tetrahydro-1-benzoxepin-5-ones (2a-d) with different benzaldehydes affords the benzylidine derivatives (3a-d) which on epoxidation followed by treatment with hydrazine hydrate and arylhydrazines furnish the title benzoxepinopyrazol