223519-11-7 Usage
General Description
5-AMINO-3-BROMO-4-METHYL-1-CARBOXYLIC ACID METHYL ESTER is a chemical compound with the molecular formula C6H8BrNO3. It is a methyl ester derivative of 5-amino-3-bromo-4-methyl-1-carboxylic acid and is commonly used in organic synthesis as an intermediate for the preparation of various pharmaceuticals and agrochemicals. 5-AMINO-3-BROMO-4-METHYL-1-CARBOXYLIC ACID METHYL ESTER is known for its reactive nature and is often used in the production of diverse organic compounds through chemical reactions such as esterification, amidation, and nucleophilic substitutions. Its structural properties and reactivity make it a valuable building block for the creation of complex molecules in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 223519-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 223519-11:
(8*2)+(7*2)+(6*3)+(5*5)+(4*1)+(3*9)+(2*1)+(1*1)=107
107 % 10 = 7
So 223519-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10BrNO2/c1-5-7(10)3-6(4-8(5)11)9(12)13-2/h3-4H,11H2,1-2H3
223519-11-7Relevant articles and documents
SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE
-
, (2019/01/21)
The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr
Synthesis of substituted 4-(1H-indol-6-yl)-1H-indazoles as potential PDK1 inhibitors
Brzozowski, Martin,O'Brien, Nathan J.,Wilson, David J.D.,Abbott, Belinda M.
, p. 318 - 326 (2014/01/06)
The development of a preparative route to a series of novel 4-(1H-indol-6-yl)-1H-indazole compounds as potential PDK1 inhibitors is described. The synthetic strategy centres on the late-stage Suzuki cross-coupling of N-unprotected indazole and indole frag
