32178-63-5 Usage
General Description
8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid, also known as methoxytetrahydronaphthoic acid, is a chemical compound with the molecular formula C13H16O3. It is a carboxylic acid derivative of tetrahydronaphthalene, and the methoxy group at the 8th position gives it a unique chemical property. 8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID is often used as a building block in the synthesis of various pharmaceuticals and biologically active molecules. It has potential applications in medicinal chemistry and drug discovery, particularly for the development of new drugs for the treatment of various diseases and disorders. The compound's structural properties and biological activities make it a valuable and versatile chemical for research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 32178-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32178-63:
(7*3)+(6*2)+(5*1)+(4*7)+(3*8)+(2*6)+(1*3)=105
105 % 10 = 5
So 32178-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O3/c1-15-11-4-2-3-8-5-6-9(12(13)14)7-10(8)11/h2-4,9H,5-7H2,1H3,(H,13,14)
32178-63-5Relevant articles and documents
Huffman,Mole
, p. 501,502 (1971)
A new synthesis of 8-hydroxy-2-di-n-propylamino-tetralin (8-OH-DPAT)
Langlois,Gaudy
, p. 1723 - 1734 (2007/10/02)
A new synthesis method for 8-OH-DPAT, a specific agonist at the 5-HT(1A) serotonin receptor, is described. It employs the Curtius degradation of a tetralin carboxylic acid easily prepared from (2-methoxy benzyl) succinic acid by Friedel-Craft cyclisation.
Studies on Gibberellin Synthesis. Assembly of an Ethanophenanthrenoid Lactone and Conversion into a Gibbane Derivative
Mander, Lewis N.,Pyne, Stephen G.
, p. 1899 - 1911 (2007/10/02)
Diazoketone (13), prepared by standard methods from 5-formyl-8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (7), was cyclized in trifluoroacetic acid to dienone (1) which underwent intramolecular 1,4-conjugate addition to afford the ethanophena
