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3-Nitrophenyl piperidine-3-carboxylate hydrochloride (1:1) is a chemical compound with the molecular formula C12H16ClN2O4. It is a salt formed from the reaction of 3-nitrophenyl piperidine-3-carboxylic acid and hydrochloric acid. 3-nitrophenyl piperidine-3-carboxylate hydrochloride (1:1) is characterized by the presence of a nitro group (-NO2) attached to a phenyl ring, a piperidine ring, and a carboxylate group (-COO-). The hydrochloride salt form indicates that it contains a chloride ion (Cl-) to balance the positive charge from the protonated carboxylic acid group. 3-nitrophenyl piperidine-3-carboxylate hydrochloride (1:1) is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. It is important to handle 3-nitrophenyl piperidine-3-carboxylate hydrochloride (1:1) with care due to its potential reactivity and the presence of a nitro group, which can be a source of concern in terms of safety and stability.

94528-08-2

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94528-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94528-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94528-08:
(7*9)+(6*4)+(5*5)+(4*2)+(3*8)+(2*0)+(1*8)=152
152 % 10 = 2
So 94528-08-2 is a valid CAS Registry Number.

94528-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-nitrophenyl) piperidine-3-carboxylate,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Nitrophenyl 3-piperidinecarboxylate hydrochloride

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:94528-08-2 SDS

94528-08-2Downstream Products

94528-08-2Relevant academic research and scientific papers

γ-Aminobutyric acid uptake inhibition and anticonvulsant activity of nipecotic acid esters

Crider,Wood,Tschappat,Hinko,Seibert

, p. 1612 - 1616 (1984)

n-Alkyl esters of nipecotic acid were prepared by Fischer esterification, and the esters were evaluated against bicuculline-induced seizures in mice. Evaluation of the alkyl esters for inhibition of γ-aminobutyric acid uptake into mouse whole brain mini-slices revealed that the order of potency was proportional to chain length. The octyl ester inhibited γ-aminobutyric acid and β-alanine uptakes by apparently nonspecific mechanisms. A variety of phenyl esters of nipecotic acid were also synthesized utilizing either dicyclohexylcarbodiimide or 1,1'-carbonyldiimidazole as the condensing agent. Most of the phenyl esters were potent inhibitors of γ-aminobutyric acid uptake. The uptake inhibition appeared to involve specific and nonspecific (detergent-like) mechanisms. The m-nitrophenyl and p-nitrophenyl esters were particularly potent against bicuculline-induced seizures in mice.

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