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Ethyl (1-benzyl-4-oxo-3-piperidinyl)acetate is a complex organic compound with the chemical formula C16H21NO3. It is a derivative of piperidine, a heterocyclic amine, and features a benzyl group attached to the nitrogen atom. The molecule contains a 4-oxo group, indicating the presence of a carbonyl group, and an acetate group, which is an ester derived from acetic acid. Ethyl (1-benzyl-4-oxo-3-piperidinyl)acetate is characterized by its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its role as an intermediate in various chemical reactions. Its structure and properties make it a valuable component in the development of new drugs and other chemical products.

6947-75-7

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6947-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6947-75-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6947-75:
(6*6)+(5*9)+(4*4)+(3*7)+(2*7)+(1*5)=137
137 % 10 = 7
So 6947-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO3/c1-2-20-16(19)10-14-12-17(9-8-15(14)18)11-13-6-4-3-5-7-13/h3-7,14H,2,8-12H2,1H3

6947-75-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(1-benzyl-4-oxopiperidin-3-yl)acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:6947-75-7 SDS

6947-75-7Relevant academic research and scientific papers

Synthesis and biological evaluation of 3,7-diazabicyclo[4.3.0]nonan-8-ones as potential nootropic and analgesic drugs

Martini, Elisabetta,Di Cesare Mannelli, Lorenzo,Bartolucci, Gianluca,Bertucci, Carlo,Dei, Silvia,Ghelardini, Carla,Guandalini, Luca,Manetti, Dina,Scapecchi, Serena,Teodori, Elisabetta,Romanelli, Maria Novella

supporting information; experimental part, p. 2512 - 2516 (2011/06/24)

A series of cis and trans 3,7-diazabicyclo[4.3.0]nonan-8-ones has been synthesized and tested for their ability to revert scopolamine-induced amnesia in the mouse passive-avoidance test. The racemates of the most potent compounds 4 and 7 were separated and tested, but no enantioselectivity was found for the nootropic activity. Compounds 4 and 7 and their enantiomers displayed interesting antihyperalgesic activity in two models of neuropathic pain (streptozotocin-induced and oxalilplatin-induced neuropathy) in comparison with pregabalin.

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