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TERT-BUTYL 6-FLUORO-3-OXO-2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE]-1'-CARBOXYLATE is a chemical compound characterized by its spiro-ring structure, which includes a piperidine and indene moiety. It is a tert-butyl ester derivative of a 6-fluoro-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylic acid. This unique structure and its properties make it a promising candidate for pharmaceutical research and drug discovery.

910442-55-6

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910442-55-6 Usage

Uses

Used in Pharmaceutical Research:
TERT-BUTYL 6-FLUORO-3-OXO-2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE]-1'-CARBOXYLATE is used as a building block for the synthesis of various bioactive molecules. Its unique structure and properties make it a valuable tool for drug discovery and development.
Used in Drug Discovery:
TERT-BUTYL 6-FLUORO-3-OXO-2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE]-1'-CARBOXYLATE is used as a valuable tool in drug discovery due to its potential to contribute to the development of new pharmaceutical compounds with therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 910442-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,4,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 910442-55:
(8*9)+(7*1)+(6*0)+(5*4)+(4*4)+(3*2)+(2*5)+(1*5)=136
136 % 10 = 6
So 910442-55-6 is a valid CAS Registry Number.

910442-55-6Upstream product

910442-55-6Downstream Products

910442-55-6Relevant academic research and scientific papers

A new synthesis of spiropyrrolidine-tetralones via an unexpected formal ring-contraction of 4-disubstituted piperidine to 3-disubstituted pyrrolidine

Bandarage, Upul K.,Davies, Robert J.

scheme or table, p. 6415 - 6417 (2011/01/03)

We have developed an efficient synthesis of novel racemic spiropyrrolidine-tetralones via an unexpected ring-contraction reaction of a 4-disubstituted piperidine to 3-disubstituted pyrrolidine. We suggest that intramolecular quaternization of the piperidi

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