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Dibenz[b,f]oxepin-10-carboxylic acid 53921-70-3 is a chemical compound belonging to the class of dibenzoxepin derivatives, characterized by its unique chemical structure and pharmacological properties. It is utilized in the pharmaceutical industry as a starting material for the synthesis of various drugs, particularly focusing on antipsychotic and antidepressant medications.

53921-70-3

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53921-70-3 Usage

Uses

Used in Pharmaceutical Industry:
Dibenz[b,f]oxepin-10-carboxylic acid 53921-70-3 is used as a starting material for the synthesis of various drugs, specifically targeting the development of antipsychotic and antidepressant medications. Its unique structure and properties make it a valuable asset in the creation of new pharmaceuticals aimed at treating mental health disorders.
Used in Mental Health Treatment:
Dibenz[b,f]oxepin-10-carboxylic acid 53921-70-3 is used as a potential therapeutic agent for conditions such as anxiety, bipolar disorder, and schizophrenia. Its pharmacological properties have been studied for their effects on mental health, indicating its potential in contributing to the treatment and management of these disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 53921-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,2 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53921-70:
(7*5)+(6*3)+(5*9)+(4*2)+(3*1)+(2*7)+(1*0)=123
123 % 10 = 3
So 53921-70-3 is a valid CAS Registry Number.

53921-70-3Relevant academic research and scientific papers

COUMPOUNDS MODULATING THE ACTIVITY OF GAPDH AND/OR IAMT

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Page 37, (2010/02/06)

Novel compounds and their use for modulationof L-Isoaspartyl (D-Aspartyl) 0-Metyltransferase and/or glyceraldehyde-3-phosphate dehydrogenase activity enable the prevention treatment or alleviation of diabetes, autoimmune diseases and neuro-degenerative diseases.. Compounds are of any of the formulae I - IV below:

Manganese(III)-Mediated Carbon-Carbon Bond Formation in the Reaction of Xanthenes with Active Methylene Compounds

Nishino, Hiroshi,Kamachi, Hironori,Baba, Harumi,Kurosawa, Kazu

, p. 3551 - 3557 (2007/10/02)

Oxidation of xanthenes with manganese(III) acetate in the presence of active methylene compounds such as 1,3-dicarbonyl compounds, malononitrile derivatives, acetone, and nitromethane selectively gives 9-substituted xanthene derivatives in good yields.A similar oxidation of thioxanthene also yields 2-(9-thioxanthenyl)-1,3-dicarbonyl compounds in 57-91 percent yields.The obtained 2-(9-xanthenyl)-1,3-dicarbonyl compounds are readily converted to 2-(9-xanthenylidene)-1,3-dicarbonyl derivatives using manganese(III) complexes or 2,3-dichloro-5,6-dicyano-1,4-benzoquinone.The mechanisms for the formation of 9-substituted xanthenes are discussed on the basis of the reaction intermediates, the electron-donating substituent effect on the xanthene ring system, effect of additives, and comparison with a reaction of radical-trapping reagents.

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