169044-96-6 Usage
Description
2-Amino-5-bromo-4-methoxy-benzoic acid methyl ester is a chemical compound with the formula C9H9BrNO4. It is a methyl ester of 2-Amino-5-bromo-4-methoxy-benzoic acid, characterized by its white to pale yellow solid appearance and sparing solubility in water, while being soluble in organic solvents. 2-Amino-5-bromo-4-methoxy-benzoic acid methyl ester is recognized for its potential as a building block in the synthesis of pharmaceutical and agrochemical products, making it a valuable intermediate for the production of a diverse array of useful compounds.
Uses
Used in Organic Synthesis:
2-Amino-5-bromo-4-methoxy-benzoic acid methyl ester is used as a key intermediate in organic synthesis for the creation of various chemical compounds. Its unique structure allows for versatile reactions, facilitating the development of new molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Amino-5-bromo-4-methoxy-benzoic acid methyl ester is utilized as a starting material for the synthesis of potential drug candidates. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the discovery and development of new medications.
Used in Agrochemical Development:
2-Amino-5-bromo-4-methoxy-benzoic acid methyl ester is also employed in the agrochemical sector as a precursor for the synthesis of compounds with pesticidal or herbicidal properties. Its integration into these products can enhance their effectiveness in agricultural applications.
Each of these uses highlights the compound's versatility and importance in the synthesis of a wide range of products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 169044-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169044-96:
(8*1)+(7*6)+(6*9)+(5*0)+(4*4)+(3*4)+(2*9)+(1*6)=156
156 % 10 = 6
So 169044-96-6 is a valid CAS Registry Number.
169044-96-6Relevant articles and documents
The Enantioselective Synthesis of Eburnamonine, Eucophylline, and 16′-epi-Leucophyllidine
Hayashida, Kohei,Korch, Katerina M.,Ngamnithiporn, Aurapat,Reimann, Christopher E.,Saito, Daisuke,Stoltz, Brian M.
supporting information, p. 17957 - 17962 (2021/07/12)
A synthetic approach to the heterodimeric bisindole alkaloid leucophyllidine is disclosed herein. An enantioenriched lactam building block, synthesized through palladium-catalyzed asymmetric allylic alkylation, served as the precursor to both hemispheres. The eburnamonine-derived fragment was synthesized through a Bischler–Napieralski/hydrogenation approach, while the eucophylline-derived fragment was synthesized by Friedl?nder quinoline synthesis and two sequential C?H functionalization steps. A convergent Stille coupling and phenol-directed hydrogenation united the two monomeric fragments to afford 16′-epi-leucophyllidine in 21 steps from commercial material.
Imidazo[1,5-a]quinazoline-5(4H)-ketone derivative as well as preparation method and application thereof
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, (2020/08/22)
The invention relates to an imidazo[1,5-a]quinazoline-5(4H)-ketone derivative as well as a preparation method and application thereof. The imidazo[1,5-a]quinazoline-5(4H)-ketone derivative disclosed by the invention can be used for preparing a BET protein
NOVEL BENZYLAMINO SUBSTITUTED QUINAZOLINES AND DERIVATIVES AS SOS1 INHIBITORS
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Page/Page column 87, (2018/07/29)
The present invention encompasses compounds of formula (I), wherein the groups R1 to R7 have the meanings given in the claims and specification, their use as inhibitors of SOS1, pharmaceutical compositions which contain compounds of this kind and their use as medicaments/medical uses, especially as agents for treatment and/or prevention of oncological diseases.
