59690-97-0 Usage
Description
10-Bromocarbamazepine, also known as 10-Bromo-5H-dibenzo[b,f]azepine-5-carboxamide, is a chemical compound derived from Carbamazepine, a well-known anticonvulsant medication. It possesses neuroprotective and neuroresearch properties, making it a valuable compound for various applications in the pharmaceutical and medical fields.
Uses
Used in Pharmaceutical Industry:
10-Bromocarbamazepine is used as an impurity in the production of Carbamazepine (C175840(P)), which is an essential medication for the treatment of pain associated with trigeminal neuralgia. Its presence in the manufacturing process helps in the development and formulation of effective anticonvulsant drugs.
Used in Neuroprotection:
10-Bromocarbamazepine serves as a neuroprotective agent, playing a crucial role in safeguarding the nervous system from damage or degeneration. Its neuroprotective properties make it a promising candidate for the development of treatments for various neurological disorders.
Used in Neuroresearch:
As a neuroresearch product, 10-Bromocarbamazepine is utilized in the study and understanding of the nervous system, its functions, and the underlying mechanisms of various neurological conditions. 10-Bromocarbamazepine aids researchers in their quest to develop new therapeutic strategies and improve existing treatments for neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 59690-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59690-97:
(7*5)+(6*9)+(5*6)+(4*9)+(3*0)+(2*9)+(1*7)=180
180 % 10 = 0
So 59690-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H11BrN2O/c16-12-9-10-5-1-3-7-13(10)18(15(17)19)14-8-4-2-6-11(12)14/h1-9H,(H2,17,19)
59690-97-0Relevant articles and documents
Synthetic method of oxcarbazepine
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Paragraph 0015, (2017/08/31)
The invention relates to a synthetic method of oxcarbazepine. According to the method, the oxcarbazepine is prepared from iminodibenzyl as a raw material through formyl chlorination, dihalogenated dehydrohalogenation, ammonification and hydrolyzation; a product obtained after formyl chlorination is iminodibenzyl-5-carbonyl chloride, wherein the dihalogenated dehydrohalogenation process specifically comprises the step that the iminodibenzyl-5-carbonyl chloride and a halogenating reagent react for 3-6 h at the temperature ranging from 80 DEG C to the reflux temperature in the presence of an organic solvent and an initiating agent to obtain a disubstituted halogenated product, then the disubstituted halogenated product reacts for 8-16 h at the reflux temperature to be subjected to dehydrohalogenation to obtain 10-halo-5H-dibenzoazepine-5-formyl chloride. The method has the advantages that starting materials are low in price and easy to obtain; the processing step is short; the yield is high; and the cost is low.