924668-99-5 Usage
Description
Methyl 5-fluoro-2-(MethylaMino)benzoate is a chemical compound with the formula C9H10FNO2. It is a fluoro-substituted benzoate ester with a methylamino group, and it is commonly used in medicinal chemistry for the synthesis of various pharmaceuticals. Methyl 5-fluoro-2-(MethylaMino)benzoate has been studied for its potential therapeutic effects, particularly in the field of neuroscience and neurological disorders. It is a white to off-white crystalline solid that is soluble in organic solvents and has a characteristic odor. Methyl 5-fluoro-2-(MethylaMino)benzoate is an important intermediate in the production of pharmaceuticals and is used in the research and development of new drugs.
Uses
Used in Pharmaceutical Industry:
Methyl 5-fluoro-2-(MethylaMino)benzoate is used as an intermediate for the synthesis of various pharmaceuticals for the treatment of neurological disorders.
Used in Medicinal Chemistry Research:
Methyl 5-fluoro-2-(MethylaMino)benzoate is used as a research compound for the development of new drugs with potential therapeutic effects in the field of neuroscience and neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 924668-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,6,6 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 924668-99:
(8*9)+(7*2)+(6*4)+(5*6)+(4*6)+(3*8)+(2*9)+(1*9)=215
215 % 10 = 5
So 924668-99-5 is a valid CAS Registry Number.
924668-99-5Relevant articles and documents
Benzopyrimidodiazepinone inhibitors of TNK2
Chen, Bailing,Feru, Frederic,Feutrill, John,Gero, Thomas W.,Gray, Nathanael S.,Groendyke, Brian J.,Li, Bin,Li, Zhengnian,Pang, Kevin,Powell, Chelsea E.,Scott, David A.,Szabo, Hilary
, (2020/01/22)
The SAR of a series of benzopyrimidodiazepinone inhibitors of TNK2 was developed, starting from the potent and selective compound XMD8-87. A diverse set of anilines was introduced in an effort to improve the in vivo PK profile and minimize the risk of quinone diimine formation.
Synthesis of xanthones, thioxanthones, and acridones by the coupling of arynes and substituted benzoates
Zhao, Jian,Larock, Richard C.
, p. 583 - 588 (2007/10/03)
The reaction of silylaryl triflates, CsF, and ortho-heteroatom-substituted benzoates affords a general and efficient way to prepare biologically interesting xanthones, thioxanthones, and acridones. This chemistry presumably proceeds by a tandem intermolecular nucleophilic coupling of the benzoate with an aryne and a subsequent intramolecular electrophilic cyclization.
