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CAS

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144282-55-3

1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144282-55-3 Structure

  • Basic information

    1. Product Name: 1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester
    2. Synonyms: 1-ethoxycarbonyl-4-methylenepiperidine;
    3. CAS NO:144282-55-3
    4. Molecular Formula: C9H15NO2
    5. Molecular Weight: 169.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144282-55-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester(144282-55-3)
    11. EPA Substance Registry System: 1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester(144282-55-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 144282-55-3(Hazardous Substances Data)

144282-55-3 Usage

Explanation

The compound is composed of 9 carbon atoms, 15 hydrogen atoms, 1 nitrogen atom, and 2 oxygen atoms.

Explanation

This name provides an alternative way to describe the compound's structure, emphasizing the presence of an ethyl ester group and a 4-oxo (or 4-methylene) functional group on the piperidine ring.

Explanation

The compound is classified as an ester due to the presence of an ester functional group (-COO-) formed by the combination of a carboxylic acid and an alcohol.

Explanation

1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, acting as a building block for creating more complex molecules.

Explanation

The compound is utilized as a building block in the creation of substances, including drugs for the treatment of central nervous system disorders, due to its chemical structure and properties.

Explanation

1-Piperidinecarboxylic acid, 4-methylene-, ethyl ester may also play a role in the development of insecticides and herbicides, as its chemical structure and properties make it valuable in the production and manipulation of diverse chemical and biological compounds.

Classification

Ester

Use as an intermediate

Synthesis of pharmaceuticals and agrochemicals

Application in central nervous system disorders

Drug development

Role in insecticides and herbicides

Development and production

Check Digit Verification of cas no

The CAS Registry Mumber 144282-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144282-55:
(8*1)+(7*4)+(6*4)+(5*2)+(4*8)+(3*2)+(2*5)+(1*5)=123
123 % 10 = 3
So 144282-55-3 is a valid CAS Registry Number.

144282-55-3SDS

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 ethyl 4-methylenepiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-ethoxycarbonyl-4-methylenepiperidine

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:144282-55-3 SDS

144282-55-3Relevant articles and documents

Development of a Robust Process for the Preparation of High-Quality 4-Methylenepiperidine Hydrochloride

Zhu, Fuqiang,Aisa, Haji A.,Zhang, Jian,Hu, Tianwen,Sun, Changliang,He, Yang,Xie, Yuanchao,Shen, Jingshan

, p. 91 - 96 (2018/02/06)

An efficient route for the preparation of 4-methylenepiperidine hydrochloride 1 was designed, and then a process feasible for large-scale production was developed with a total yield of 83.5% at a purity of 99.9%.

Tandem hydroformylation-hydrazone formation-Fischer indole synthesis: A novel approach to tryptamides

Schmidt, Axel M.,Eilbracht, Peter

, p. 2333 - 2343 (2007/10/03)

A novel one-pot synthesis of indole systems via tandem hydroformylation-hydrazone formation-Fischer indolization starting from allylic amides and aryl hydrazines is described. This tandem procedure directly leads to biologically interesting tryptamides and analogues. The Royal Society of Chemistry 2005.

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