88340-85-6 Usage
Uses
Used in Organic Synthesis:
(2E,5Z)-2-[(DIMETHYLAMINO)METHYLENE]-5-[(2Z)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]CYCLOPENTANONE is used as a reactive intermediate in organic synthesis for [application reason]. Its conjugated carbon-carbon double bonds and various functional groups make it a promising candidate for the development of new organic compounds and materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2E,5Z)-2-[(DIMETHYLAMINO)METHYLENE]-5-[(2Z)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]CYCLOPENTANONE is used as a starting material for the development of new drugs for [application reason]. Its unique structure and functional groups may contribute to the discovery of novel therapeutic agents with potential applications in various medical fields.
Used in Chemical Research:
(2E,5Z)-2-[(DIMETHYLAMINO)METHYLENE]-5-[(2Z)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]CYCLOPENTANONE is utilized in chemical research as a model compound to study [application reason]. Its complex structure and functional groups provide opportunities for investigating various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 88340-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,4 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88340-85:
(7*8)+(6*8)+(5*3)+(4*4)+(3*0)+(2*8)+(1*5)=156
156 % 10 = 6
So 88340-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H26N2O/c1-21(2)17-8-6-7-9-18(17)23(5)19(21)13-12-15-10-11-16(20(15)24)14-22(3)4/h6-9,12-14H,10-11H2,1-5H3/b15-12-,16-14+,19-13-
88340-85-6Relevant academic research and scientific papers
POLYMETHINE DYES WITH HYDROCARBON BRIDGES. ENAMINO KETONES IN THE CHEMISTRY OF CYANINE DYES
Slominskii, Yu. L,Radchenko, I. D.,Popov, S. V.,Tolmachev, A. I.
, p. 1854 - 1860 (2007/10/02)
In the presence of bases alicyclic enamino ketones can react both with methyl- and with β-dialkylaminovinyl-substituted quaternary salts of nitrogen heterocycles.The reaction leads to the formation of merocyanines in which part of the chromophore extends
