412947-54-7 Usage
Description
Methyl 3-amino-4-iodobenzoate is an organic compound that serves as a crucial intermediate in various chemical and pharmaceutical processes. It is characterized by its unique molecular structure, which features a benzene ring with an amino group at the 3-position and an iodine atom at the 4-position, attached to a methyl ester group. methyl 3-amino-4-iodobenzoate is known for its versatile reactivity and potential applications in different industries.
Uses
Used in Organic Synthesis:
Methyl 3-amino-4-iodobenzoate is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows for a range of chemical reactions, making it a valuable building block in the creation of complex molecules.
Used in Pharmaceuticals:
In the pharmaceutical industry, methyl 3-amino-4-iodobenzoate is used as a starting material for the development of new drugs. Its versatile chemical properties enable the synthesis of a wide array of pharmaceutical compounds, contributing to the advancement of medical treatments.
Used in Agrochemicals:
Methyl 3-amino-4-iodobenzoate is also utilized in the agrochemical sector, where it serves as a vital component in the production of various agrochemical products. Its application in this industry helps improve the efficiency and effectiveness of agricultural chemicals.
Used in Dyestuff:
In the dyestuff industry, methyl 3-amino-4-iodobenzoate is employed as a raw material for the synthesis of dyes and pigments. Its unique molecular structure contributes to the development of novel colorants with improved properties, such as enhanced color strength and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 412947-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,9,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 412947-54:
(8*4)+(7*1)+(6*2)+(5*9)+(4*4)+(3*7)+(2*5)+(1*4)=147
147 % 10 = 7
So 412947-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8INO2/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4H,10H2,1H3
412947-54-7Relevant articles and documents
Preparation of 3-substituted-2-pyridin-2-ylindoles: regioselectivity of Larock's indole annulation with 2-alkynylpyridines
Roschangar, Frank,Liu, Jianxiu,Estanove, Emilie,Dufour, Marine,Rodríguez, Sonia,Farina, Vittorio,Hickey, Eugene,Hossain, Azad,Jones, Paul-James,Lee, Heewon,Lu, Bruce Z.,Varsolona, Richard,Schr?der, Jürgen,Beaulieu, Pierre,Gillard, James,Senanayake, Chris H.
, p. 363 - 366 (2008/09/17)
A regioselective Larock approach to 3-substituted-2-pyridin-2-ylindoles from 2-alkynylpyridines and 2-iodoanilines is described herein. The unexpectedly high regioselectivity can be rationalized by a combination of steric, coordinative and electronic effects.
1,1,1-TRIFLUORO-4-PHENYL-4-METHYL-2-(1H-PYRROLO
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Page/Page column 189, (2010/02/11)
Compounds of Formula (IA), IB), IC), and (ID) wherein R1, R2, R3, R4, R5, and R6 are as respectively defined herein for Formula (IA), (IB), (IC), and (ID), or a tautomer, prodrug, solvate, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.
Stereoselective synthesis of (E)-3-(methoxycarbonyl)methylene-1,3-dihydroindol-2-ones by palladium-catalyzed oxidative carbonylation of 2-ethynylanilines
Gabriele, Bartolo,Salerno, Giuseppe,Veltri, Lucia,Costa, Mirco,Massera, Chiara
, p. 4607 - 4613 (2007/10/03)
A direct synthesis of (E)-3-(methoxycarbonyl)methylene-1,3-dihydroindol-2-ones 2 by palladium-catalyzed oxidative carbonylation of 2-ethynylanilines 1 is reported. Reactions were carried out in MeOH as the solvent at 50-70°C in the presence of catalytic a
