99282-79-8 Usage
Description
2-(Carboxymethyl-amino)-4-chloro-benzoic acid is a chemical compound that features a benzoic acid core with a carboxymethyl-amino group and a chlorine atom attached to the benzene ring. This structure endows the compound with unique properties, such as the potential to act as a chelating agent due to the carboxymethyl-amino group, and additional reactivity due to the chlorine atom. It is widely recognized for its applications in the synthesis of pharmaceuticals and agrochemicals, as well as in metal extraction and purification processes.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-(Carboxymethyl-amino)-4-chloro-benzoic acid is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a diverse range of compounds with potential therapeutic and pesticidal properties.
Used in Metal Extraction and Purification Processes:
As a potential chelating agent, 2-(Carboxymethyl-amino)-4-chloro-benzoic acid is used in metal extraction and purification processes. Its ability to form bonds with metal ions makes it a valuable tool in these applications, enhancing the efficiency of metal recovery and purification.
Used in Organic Synthesis:
The chlorine atom in 2-(Carboxymethyl-amino)-4-chloro-benzoic acid provides the compound with additional reactivity, making it a useful intermediate in organic synthesis. This allows for further functionalization and the development of new compounds with a variety of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 99282-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99282-79:
(7*9)+(6*9)+(5*2)+(4*8)+(3*2)+(2*7)+(1*9)=188
188 % 10 = 8
So 99282-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClNO4/c10-5-1-2-6(9(14)15)7(3-5)11-4-8(12)13/h1-3,11H,4H2,(H,12,13)(H,14,15)
99282-79-8Relevant articles and documents
N-heterocyclic carbene-catalyzed enantioselective annulation of indolin-3-ones with bromoenals
Ni, Qijian,Song, Xiaoxiao,Raabe, Gerhard,Enders, Dieter
supporting information, p. 1535 - 1538 (2014/06/09)
N-Heterocyclic carbene-catalyzed reactions of indolin-3-ones with 2-bromoenals opened an asymmetric access to 3,4-dihydropyrano[3,2-b]indol-2(5 H)-ones in good yields and with good to excellent enantioselectivities. This protocol tolerates a broad substrate scope. In addition, a possible mechanism for the annulation reaction is presented. More NHC-organocatalysis: N-Heterocyclic carbene-catalyzed reactions of indolin-3-ones with 2-bromoenals opened an asymmetric access to 3,4-dihydropyrano[3,2-b]indol-2(5 H)-ones in good yields and with good to excellent enantioselectivities. This protocol tolerates a broad substrate scope. In addition, a possible mechanism for the annulation reaction is presented.
BENZYL-SUBSTITUTED TETRACYCLIC HETEROCYCLIC COMPOUNDS AS PDE5 INHIBITORS
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Page/Page column 107, (2010/04/03)
The present invention pertains to Benzyl-substituted tetracyclic heterocyclic compounds, as well as the resulting pharmaceutical compositions, and their use in the treatment or prophylaxis of diseases alleviated by inhibition of type 5 phosphodiesterases. Furthermore, the present invention pertains to the methods of manufacturing these Benzyl-substituted tetracyclic heterocyclic compounds.
An improved synthesis of 1-acetyl-1H-indol-3-yl acetates
Rodriguez-Dominguez, Juan C.,Balbuzano-Deus, Alexander,Lopez-Lopez, Miguel A.,Kirsch, Gilbert
, p. 273 - 275 (2008/03/14)
(Chemical Equation Presented) An efficient two steps procedure for the synthesis of 1-acetyl-1H-indol-3-yl acetates, starting from 2-chlorobenzoic acids, was developed and in general, moderate to good yields were obtained.
