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1(2H)-Pyridinecarboxylicacid,ethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57956-33-9

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57956-33-9 Usage

Derivation

Synthetic ester derived from nicotinic acid and ethanol.

Industry Applications

Commonly used in the pharmaceutical and cosmetic industries.

Function

Acts as a vasodilator and rubefacient.

Mechanism of Action

Increases blood flow to the skin, improving circulation and relieving symptoms of various skin conditions.

Topical Analgesic

Used in topical analgesic products for temporary relief from minor aches and pains.

Oral Health Products

Utilized in some over-the-counter oral health products for its reported anti-inflammatory and antiseptic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 57956-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,5 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57956-33:
(7*5)+(6*7)+(5*9)+(4*5)+(3*6)+(2*3)+(1*3)=169
169 % 10 = 9
So 57956-33-9 is a valid CAS Registry Number.

57956-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2H-pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-ethoxycarbonyl-1,2-dihydropyridine

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:57956-33-9 SDS

57956-33-9Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR PARASITE CONTROL

-

Page/Page column 55; 93, (2022/01/05)

The present invention relates in its broadest aspect to a compound of Formula I as provided herein, formulations comprising such a compound and corresponding uses thereof for the reduction of infestation with ectoparasites, in particular ectoparasites of the insect class, including fleas and mosquitoes and/or ectoparasites of the arachnid class, including ticks and mites, etc. Also provided herein are methods for preparing the formulations of the invention and methods for controlling ectoparasites using the compounds and/or formulations provided herein.

Reductive Heck coupling: An efficient approach toward the iboga alkaloids. Synthesis of ibogamine, epiibogamine and iboga analogs

Jana, Goutam Kumar,Sinha, Surajit

supporting information; experimental part, p. 1671 - 1674 (2012/04/11)

A mild and efficient synthetic route to the iboga scaffold by employing reductive-Heck type annulation is described. The utility of this process is demonstrated by the direct access to the ibogamine, epiibogamine and iboga-analogs. The cyclization precursors were readily obtained from 2-iodoaniline by heteroannulation reaction with suitable alkynes followed by iodination.

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