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methyl 4-(2-fluorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

292852-18-7

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292852-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292852-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,5 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 292852-18:
(8*2)+(7*9)+(6*2)+(5*8)+(4*5)+(3*2)+(2*1)+(1*8)=167
167 % 10 = 7
So 292852-18-7 is a valid CAS Registry Number.

292852-18-7Downstream Products

292852-18-7Relevant academic research and scientific papers

One-pot multicomponent synthesis hexahydroquinoline derivatives in Triton X-100 aqueous micellar media

Poor Heravi, Mohammad Reza,Mehranfar, Shadi,Shabani, Nemat

, p. 141 - 145 (2014)

A facile and efficient synthesis of hexahydroquinoline derivatives (5a-o) was reported via a four-component condensation reaction of aldehydes, dimedone, methyl aceto acetate and ammonium acetate in the presence of Triton X-100 in water at room temperature. The use of just 20 mol % of Triton X-100 in water solvent is sufficient. The FT-IR, 19F NMR, 1H NMR, 13C NMR spectra and elemental analysis confirm the structure of the compounds.

Cobalt triflate catalyzed one-pot synthesis of fluorophore 1,4-dihydropyridine derivatives via Hantzsch reaction

Bagdi, Prasanta Ray,Basha, R. Sidick,Lal, Mohan,Misra, Rajkumar,Khan, Abu T.

, p. 1589 - 1598 (2014/01/17)

A wide variety of 1,4-dihydropyridines have been synthesized through one-pot condensation of aromatic aldehydes, β-ketoesters, cyclic 1,3-diones and ammonium acetate using cobalt triflate as a catalyst through Hantzsch reaction. Some of the salient features of the present protocol are shorter reaction time, mild reaction conditions, good yields, non-aqueous work-up, reusability of the catalyst and non-requirement of column chromatographic separation.

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