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111054-55-8

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111054-55-8 Usage

Description

1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-hydroxy-, ethyl ester, also known as ethyl 3,4-dihydro-2-hydroxy-1H-pyridine-4-carboxylate, is an organic compound that is a carboxylic acid ester and a derivative of pyridine. It is characterized by its potential applications in various industries, including pharmaceuticals, agrochemicals, and the production of flavor and fragrance compounds.

Uses

Used in Pharmaceutical Synthesis:
1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-hydroxy-, ethyl ester is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic properties. It may contribute to the development of treatments for neurodegenerative diseases and certain types of cancer.
Used in Agrochemical Production:
In the agrochemical industry, 1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-hydroxy-, ethyl ester is used as a building block in the creation of various agrochemical products, potentially enhancing their effectiveness and performance.
Used in Flavor and Fragrance Compounds:
This chemical is also utilized in the production of flavor and fragrance compounds, where its unique properties can contribute to the development of novel and improved scents and tastes.
Safety Precautions:
It is important to handle 1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-hydroxy-, ethyl ester with caution, as it can be harmful if ingested or inhaled, and can cause skin and eye irritation. Proper safety measures should be taken during its use and storage to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 111054-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,5 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111054-55:
(8*1)+(7*1)+(6*1)+(5*0)+(4*5)+(3*4)+(2*5)+(1*5)=68
68 % 10 = 8
So 111054-55-8 is a valid CAS Registry Number.

111054-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-hydroxy-3,4-dihydro-2H-pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1(2H)-Pyridinecarboxylic acid,3,4-dihydro-2-hydroxy-,ethyl ester

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:111054-55-8 SDS

111054-55-8Downstream Products

111054-55-8Relevant articles and documents

Facile Access to 6-Methoxy-1,2,3,6-tetrahydro- and 4-Hydroxy-1,2,3,4-tetrahydropyridines by Electrochemical Haloalkoxylation-Dehydrohalogenation Sequence as a Key Operation

Torii, Sigeru,Inokuchi, Tsutomu,Akahosi, Fumihiko,Kubota, Minoru

, p. 242 - 245 (2007/10/02)

A facile procedure for the synthesis of N-ethoxycarbonyl-6-methoxy-1,2,3,6-tetrahydropyridines 6 and N-ethoxycarbonyl-4-hydroxy-1,2,3,4-tetrahydropyridines 7 from piperidines 1 is described.The electrochemical halomethoxylation of N-ethoxycarbonyl-1,2,3,4-tetrahydropyridines 4 (easily accessible from 1 by ethoxycarbonylation followed by electrooxidative methoxylation and acid-catalyzed elimination of methanol) in a CH3OH-NR4X (X=Cl, Br, I)-(Pt)-(Pt) system provides N-ethoxycarbonyl-3-halo-2-methoxypiperidines 5 in 74-90percent yields.Dehydrohalogenation of iodides 5 (X=I)with 1,8-diazabicycloundec-7-ene (DBU) in toluene gave the desired olefin 6, which was isomerized in aqueous acetic acid to afford the alcohol 7 in 34-55percent yields (from 5).The procedure is also applicable to the synthesis of seven membered derivatives 6f and 7f from 1f.

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