141104-65-6 Usage
Description
1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) is a chemical compound with the molecular formula C13H15NO2. It is an ethyl ester derivative of 1H-Indene-2-carboxylic acid, containing an amino group and a 2,3-dihydro-1H-indene ring structure. 1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) is known for its potential applications in the pharmaceutical industry and organic synthesis.
Used in Pharmaceutical Industry:
1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) is used as a precursor for the synthesis of various drugs, particularly those targeting neurological disorders. Its unique structure and functional groups make it a valuable building block for the development of new therapeutic agents.
Used in Organic Synthesis:
1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) is also used in organic synthesis for the preparation of complex organic molecules. Its versatile structure allows for various chemical reactions, making it a useful intermediate in the synthesis of a wide range of compounds.
Used in Medicinal Chemistry:
Due to its potential applications in drug discovery and chemical synthesis, 1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) is an important compound for research and development in the field of medicinal chemistry. Its properties and potential uses contribute to the advancement of new drug candidates and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 141104-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141104-65:
(8*1)+(7*4)+(6*1)+(5*1)+(4*0)+(3*4)+(2*6)+(1*5)=76
76 % 10 = 6
So 141104-65-6 is a valid CAS Registry Number.
141104-65-6Relevant articles and documents
Synthesis of indan-based unusual α-amino acid derivatives under phase-transfer catalysis conditions
Kotha, Sambasivarao,Brahmachary, Enugurthi
, p. 1359 - 1365 (2000)
Conformationally constrained cyclic a-amino acid derivatives were synthesized under solid-liquid phase-transfer catalysis conditions. This methodology involves the bis-alkylation of ethyl isocyanoacetate with various a,a'-dibromo-o-xylene derivatives [a,a'-dibromo-o-xylene 5, 2,3-bis(bromomethyl)-l,4-dimethoxybenzene 6, l,2-bis(bromomethyl)-4,5-dibromobenzene 7,2,3-bis(bromomethyl)naphthalene 8, l,8-bis(bromomethyl)-naphthalene 9, 6,7-bis(bromomethyl)-2,2-dimethyl-lJ/phenalene-l,3(2H)-dione 10,2,3-bis(bromomethyl)-l,4-anthraquinone 11,6,7-bis(bromomethyl)quinoxaline 12, 3,4-bis(bromomethyl)furan 13, l,2,4,5-tetrakis(bromomethyl)benzene 28, and hexakis(bromomethyl)benzene 30] using potassium carbonate as a base and tetrabutylammonium hydrogensulfate as a phase-transfer catalyst to give corresponding isonitrile derivatives, which upon hydrolysis with HC1 in ethanol gave amino esters. Using this method electron-deficient as well as electron-rich and halogen-substituted indan-based a-amino acids were prepared. The preparation of bis-indan as well as tris-indan a-amino esters is also described.
Organic crystal engineering with piperazine-2,5-diones. 1. Crystal packing of piperazinediones derived from substituted 2-aminoindan-2- carboxylic acids
Williams, Lawrence J.,Jagadish,Lyon, Scott R.,Kloster, Robin A.,Carducci, Michael D.,Mash, Eugene A.
, p. 14281 - 14300 (2007/10/03)
We have postulated that molecules engineered to participate in three chemically distinct and linearly independent intermolecular interactions will self-assemble in a predictable fashion. Six prototypes for molecules capable of manifesting such interaction