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N-(1-Ethyl-piperidin-3-yl)-2-methoxy-5-nitro-benzamide is a complex organic compound with the molecular formula C16H22N2O4. It is characterized by a benzamide structure, where the benzene ring is substituted with a nitro group at the 5-position and a methoxy group at the 2-position. The amide group is connected to a 1-ethyl-piperidin-3-yl moiety, which adds to the molecule's complexity. N-(1-Ethyl-piperidin-3-yl)-2-methoxy-5-nitro-benzamide is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents, due to its structural features that may interact with biological targets. It is important to note that the specific applications, safety, and efficacy of N-(1-Ethyl-piperidin-3-yl)-2-methoxy-5-nitro-benzamide would be subject to further research and clinical studies.

4840-67-9

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4840-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4840-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4840-67:
(6*4)+(5*8)+(4*4)+(3*0)+(2*6)+(1*7)=99
99 % 10 = 9
So 4840-67-9 is a valid CAS Registry Number.

4840-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-ethylpiperidin-3-yl)-2-methoxy-5-nitrobenzamide

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

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More Details:4840-67-9 SDS

4840-67-9Relevant academic research and scientific papers

POTENTIAL NEUROLEPTICS OF THE ORTHOPRAMIDE SERIES; SYNTHESIS OF HETEROCYCLIC 5-AMINO-2-METHOXYBENZAMIDES AND OF SOME RELATED COMPOUNDS

Valenta, Vladimir,Holubek, Jiri,Svatek, Emil,Matousova, Oluse,Metysova, Jirina,Protiva, Miroslav

, p. 1297 - 1310 (2007/10/02)

2-Methoxy-5-nitrobenzoyl chloride was reacted with 2-(aminoethyl)-1-ethylpyrrolidine, 3-amino-1-ethylpiperidine, 4-amino-1-benzylpiperidine, 1-benzylpiperazine, and 1-amino-4-benzylpiperazine and gave the N-substituted 2-methoxy-5-nitrobenzamides VIa-VIe.Their reduction with hydrazine hydrate and Raney nickel in ethanol afforded the corresponding 5-amino-2-methoxybenzamides VIIa-VIIe.The amino amides VIIb and VIIc were transformed to methylamino compounds XIb and XIc via the 4-toluenesulfonamides VIIIb and VIIIc and the N-methyl-4-toluenesulfonamides Xb and Xc.The N-(1-benzyl-4-piperidinyl)amides VIc, VIIc, and XIc were found to be mild neuroleptics having antiapomorphine, some cataleptic and some ataxic activity.

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