42899-29-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(3,4,5,6,7,8-hexahydroquinolin-1(2H)-yl)ethanone is used as an intermediate for the production of pharmaceuticals. Its versatile chemical properties allow it to be a key component in the synthesis of a wide range of complex molecules, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(3,4,5,6,7,8-hexahydroquinolin-1(2H)-yl)ethanone is used as an intermediate in the production of various agrochemicals. Its ability to be transformed into different chemical structures makes it a valuable asset in the development of new products for agricultural applications.
Used in Fine Chemicals Industry:
1-(3,4,5,6,7,8-hexahydroquinolin-1(2H)-yl)ethanone is also utilized as an intermediate in the synthesis of fine chemicals. Its versatility in chemical transformations enables the creation of specialized compounds for use in various industries, such as fragrances, dyes, and other specialty applications.
Used in Medicinal Research:
1-(3,4,5,6,7,8-hexahydroquinolin-1(2H)-yl)ethanone has been studied for its potential medicinal properties. It is being investigated for its therapeutic effects in the treatment of various conditions, making it a promising candidate for future pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 42899-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42899-29:
(7*4)+(6*2)+(5*8)+(4*9)+(3*9)+(2*2)+(1*9)=156
156 % 10 = 6
So 42899-29-6 is a valid CAS Registry Number.
42899-29-6Relevant academic research and scientific papers
ENAMINE CHEMISTRY-XXV REDUCTION OF ENAMINONONES BY LiAlH4 AND NaBH4 SYNTHESIS OF α,β-UNSATURATED ALDEHYDES
Carlsson, S.,Lawesson, S.-O.
, p. 413 - 417 (2007/10/02)
Cyclohexanone, 2-methyl-cyclohexanone and 4-methyl-cyclohexanone, 1, were transformed into the enaminones 4a-4e by the following two routes: (A): Acylation of the enamines, 2, derived from 1 and secondary amines (pyrrolidine, morpholine and piperidine) by ethyl chloroformate, and (B): Condensation of 1 with diethyl oxalate, giving the β-ketoesters 3, followed by reaction with the secondary amines.Ethyl 2(-1-pyrrolidinyl)-1-cyclopentene-1-carboxylate. 4f, and methyl 3-(1-pyrrolidinyl)-2-buteonate, 4g, were prepared from ethyl 2-oxo-1-cyclopentanecarboxylate and ethyl 3-oxo-butanoate, respectively, by condensation with pyrrolidine.Reduction of 4a by LAH afforded 1-cyclohexen-1-carboxaldehyde, 5a, 1-cyclohexene-1-methanol, 6a, and 1-(1-cyclohexene-1-methyl)pyrrolidine, 7a, in yields depending on the molar ratio of LAH/4a.Reduction of 4f by LAH gave cyclopenten-1-methanol, 6b, 1-(1-cyclopentene-1-methyl)pyrrolidine, 7b, and ethyl-2(1-pyrrolidinyl)-1-cyclopentanecarboxylate, 8b.Compound 4g, when reduced with LAH, yielded methyl 3-(1-pyrrolidinyl) butanoate, 8c (main product) and 1-(2-butenyl)pyrrolidine, 7c (minor).Reduction of 4 by NaBH4 afforded exlusively the saturated β-aminoesters, 8, in high yields.The reductions with LAH and NaBH4 are rationalized in terms of the HSAB principle.
