109839-13-6 Usage
Description
2H-Isoindole-1-carboxylic acid is a chemical compound with the molecular formula C9H7NO2. It is an organic compound and a derivative of isoindole, a bicyclic heterocyclic compound. 2H-Isoindole-1-carboxylic acid is significant in organic chemistry and serves as a building block for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it possesses anti-inflammatory and antitumor properties, which make it a promising candidate for the development of new drugs to treat a range of diseases. The unique chemical structure and properties of 2H-Isoindole-1-carboxylic acid render it a valuable compound for diverse chemical and pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
2H-Isoindole-1-carboxylic acid is used as a key intermediate in the synthesis of pharmaceuticals for its potential role in developing new drugs with anti-inflammatory and antitumor properties. Its incorporation into drug formulations can lead to the creation of novel therapeutics for the treatment of various diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 2H-Isoindole-1-carboxylic acid is utilized as a building block for the development of new agrochemicals. Its unique structure allows for the creation of compounds that can be used in pest control, crop protection, and other agricultural applications, thereby enhancing crop yields and quality.
Used in Organic Chemistry Research:
2H-Isoindole-1-carboxylic acid serves as a valuable compound in organic chemistry research. It is used as a starting material or a synthetic intermediate for the preparation of complex organic molecules, contributing to the advancement of organic synthesis and the discovery of new chemical entities with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 109839-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,3 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109839-13:
(8*1)+(7*0)+(6*9)+(5*8)+(4*3)+(3*9)+(2*1)+(1*3)=146
146 % 10 = 6
So 109839-13-6 is a valid CAS Registry Number.
109839-13-6Relevant articles and documents
Regioselectivity of Pyrrole Synthesis fromm Diethyl Aminomalonate and 1,3-Diketones: Further Observations
Paine, John B.,Brough, Jonathan R.,Buller, Kathy K.,Erikson, Erika E.
, p. 3986 - 3993 (2007/10/02)
1,3-Diketones 1 react with diethyl aminomalonate (2) in boiling acetic acid to afford ethyl 2-pyrrolecarboxylates 6.Considerable regioselectivity was noted for the following classes of diketone: 2-acylcyclohexanones 10a,b , 2-acylcyclopentanones 10c,d pyrroles 13a,b>, 1-phenyl-2-alkyl-1,3-alkanediones 17a-d , 3-phenyl-2,4-hexanedione (21a) , 1-phenyl-3-alkyl-2,4-alkanediones 24a,b , and 2,2-dimethyl-3,5-alkanediones 29a,b .The yields varied with the structural class, decreasing with increased steric hindrance.The product structure correlated with the structure of the enolized diketones in the case of the 2-acylcycloalkanones studied.
