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1(2H)-Pyridinecarboxylic acid, 2-ethenyl-3,4-dihydro-4-oxo-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335265-99-1

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335265-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335265-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,2,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 335265-99:
(8*3)+(7*3)+(6*5)+(5*2)+(4*6)+(3*5)+(2*9)+(1*9)=151
151 % 10 = 1
So 335265-99-1 is a valid CAS Registry Number.

335265-99-1Relevant articles and documents

CYCLIC AMINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Page 47, (2008/06/13)

A compound of formula (I) wherein R represents a radical selected from i) ii) iii) iv) where the substituents R1, R2, R3, R4, R4, R7 and the indices m, n and p are as defined in the description; or pharmaceutically acceptable salts and solvates

Synthesis of Bridged Azabicyclic Structures via Ring-Closing Olefin Metathesis

Neipp, Christopher E.,Martin, Stephen F.

, p. 8867 - 8878 (2007/10/03)

A new strategy for the facile synthesis of azabicyclo[m.n.1]alkenes (m = 3-5; n = 3, 2) has been developed that involves the ring-closing metathesis (RCM) reaction of cis-2,6-dialkenyl-N-acyl piperidine derivatives. The requisite 2,6-dialkenylpiperidines may be readily prepared in six steps starting from glutarimide (11) or three steps from 4-methoxypyridine (25). In one example that establishes the practical utility of the procedure, the functionalized 8-azabicyclo [3.2.1] octane 32, which is a potential intermediate for the syntheses of various tropane alkaloids, was prepared. Additionally, a new route for the construction of the bridged tetrahydro-β-carboline ring system 5 has been developed that features the ring-closing metathesis of the enyne 45 to construct the bridging ring in 46. This concise route to 46 also features a potentially general and useful procedure for the one-step preparation of a terminal alkyne from an ester function. Selective oxidation of the vinyl group in 46 afforded the unsaturated aldehyde 47, which may serve as a useful intermediate in syntheses of several Sarpagine alkaloids.

A ring-closing olefin metathesis approach to bridged azabicyclic structures

Neipp, Christopher E,Martin, Stephen F

, p. 1779 - 1782 (2007/10/03)

A facile and general entry to functionalized bridged bicyclic nitrogen heterocycles has been developed that involves the ring-closing metathesis (RCM) of cis-2,6-dialkenyl-N-acyl piperidines that were readily prepared from glutarimide or 4-methoxypyridine

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