881909-58-6 Usage
General Description
Methyl 4-amino-3-(benzyloxy)-5-bromobenzenecarboxylate is a chemical compound that is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceutical products. It is a derivative of benzoic acid, containing a bromine atom and an amino group, as well as a methoxy group attached to a benzene ring. Methyl 4-amino-3-(benzyloxy)-5-bromobenzenecarboxylate is commonly used in the production of medications for the treatment of various medical conditions, including cancer and infectious diseases. Its unique chemical structure makes it valuable for the development of new pharmaceuticals with enhanced therapeutic properties. Additionally, it may also have potential applications in other industries, such as agrochemicals and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 881909-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,9,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 881909-58:
(8*8)+(7*8)+(6*1)+(5*9)+(4*0)+(3*9)+(2*5)+(1*8)=216
216 % 10 = 6
So 881909-58-6 is a valid CAS Registry Number.
881909-58-6Relevant articles and documents
NOVEL HYDROXYETHYLAMINE AND KETONE COMPOUNDS HAVING ASP2 INHIBITORY ACTIVITY
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, (2008/06/13)
The present invention relates to novel hydroxyethylamine and ketone compounds having Asp2 (β-secretase, BACE1 or Memapsin-2) inhibitory activity, processes for their preparation, to compositions containing them and to their use in the treatment of disease
Synthesis of 3,5,7-substituted indoles via heck cyclisation
Charrier, Nicolas,Demont, Emmanuel,Dunsdon, Rachel,Maile, Graham,Naylor, Alan,O'Brien, Alistair,Redshaw, Sally,Theobald, Pam,Vesey, David,Walter, Daryl
, p. 3071 - 3074 (2007/10/03)
Traditional strategies in indole chemistry do not allow high yielding access to some substitution patterns such as 3,5,7-trisubstituted indoles. We report in this article the efficient synthesis of this type of indole. The Heck cyclisation strategy we use