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141104-65-6

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141104-65-6 Usage

General 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 commonly used in the pharmaceutical industry as a precursor for the synthesis of various drugs, particularly those targeting neurological disorders. It may also have potential applications in organic synthesis and medicinal chemistry. The properties and potential uses of 1H-Indene-2-carboxylicacid,2-amino-2,3-dihydro-,ethylester(9CI) make it an important compound for research and development in the field of drug discovery and chemical synthesis.

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.

141104-65-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-aminoindan-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2-amino-2,3-dihydro-1H-indene-2-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:141104-65-6 SDS

141104-65-6Upstream product

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

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