86031-43-8 Usage
Methyl Ester Derivative
1H-Indene-5-carboxylic acid, 2,3-dihydro-, methyl ester is a methyl ester derivative of 1H-indene-5-carboxylic acid, which means it has a methyl group (CH3) attached to the carboxyl group (-COOH) of the parent compound.
Aromatic Hydrocarbon Indene
The compound is derived from the aromatic hydrocarbon indene, which is a six-membered ring with four double bonds and two additional carbon atoms.
Organic Synthesis
1H-INDENE-5-CARBOXYLIC ACID, 2,3-DIHYDRO-, METHYL ESTER is commonly used in organic synthesis, which involves the construction of complex organic molecules from simpler precursors.
Building Block for Pharmaceuticals and Agrochemicals
The compound serves as a building block for the production of various pharmaceuticals and agrochemicals, which are chemicals used in agriculture to protect crops from pests and diseases.
Biological and Pharmacological Properties
1H-INDENE-5-CARBOXYLIC ACID, 2,3-DIHYDRO-, METHYL ESTER has been studied for its potential biological and pharmacological properties, including its effects on the central nervous system.
New Materials and Polymers Development
The compound has been investigated for its potential use in the development of new materials and polymers, which could have a wide range of applications in various industries.
Diverse Applications
1H-INDENE-5-CARBOXYLIC ACID, 2,3-DIHYDRO-, METHYL ESTER has diverse applications in the fields of chemistry, pharmaceuticals, and materials science, making it an important compound for research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 86031-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,3 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86031-43:
(7*8)+(6*6)+(5*0)+(4*3)+(3*1)+(2*4)+(1*3)=118
118 % 10 = 8
So 86031-43-8 is a valid CAS Registry Number.
86031-43-8Relevant articles and documents
DIENAMINES AS DIELS-ALDER DIENES. A NOVEL BENZANNULATION SEQUENCE.
Snowden, Roger L.,Wust, Manfred
, p. 703 - 704 (1986)
Diels-Alder reaction between (E)-dienamines 1-7 and methyl propiolate followed by elimination of Me2NH from the intermediate cycloadducts III affords the aromatic methyl esters 8-14 in good yield.
Synthesis of substituted benzenes and phenols by ring-closing olefin metathesis
Yoshida, Kazuhiro,Takahashi, Hidetoshi,Imamoto, Tsuneo
experimental part, p. 8246 - 8261 (2009/09/29)
New synthetic approaches to substituted aromatic compounds are reported. Ring-closing olefin metathesis (RCM)/dehydration and RCM/tautomerization are the key processes in the synthesis of substituted benzenes 3 and phenols 6, respectively. Readily accessible 1,5,7-trien-4-ols 7, which are the precursors of benzenes, were prepared from β-halo-α, β-unsaturated aldehydes 11 or β-halo-α,β-unsaturated esters 19 by utilizing reliable transformations in which cross-coupling with vinylic metal reagents 12 and allylation with allylic metal reagents 13 were employed as carbon-carbon bond forming reactions. RCM of 7, followed by dehydration, afforded a wide variety of substituted benzenes 3. In addition, RCM of 1,5,7trien-4-ones 9, which were prepared by oxidation of 7, furnished various substituted phenols 6 by automatic tautomerization.
Syntheses of compounds active toward glutamate receptors: I. New preparative synthesis of aminoindandicarboxylic acid (AIDA)
Matveeva,Podrugina,Zefirova,Alekseev,Bachurin,Pellicciari,Zefirov
, p. 1764 - 1768 (2007/10/03)
A preparative procedure has been developed for the synhtesis of 1-aminoindan-1,5-dicarboxylic acid which is a new group I metabotropic glutamate receptor antagonist.
