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CAS

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101327-98-4

Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is a chemical compound with the molecular formula C8H13NO3, belonging to the piperidine derivatives and featuring a methyl ester group. This white, crystalline solid has a molecular weight of 171.19 g/mol and is commonly utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a reagent in organic synthesis reactions.

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  • 101327-98-4 Structure

  • Basic information

    1. Product Name: Methyl 1-Methyl-2-oxopiperidine-3-carboxylate
    2. Synonyms: Methyl 1-Methyl-2-oxopiperidine-3-carboxylate;1-Methyl-2-oxo-3-piperidinecarboxylic acid methyl ester
    3. CAS NO:101327-98-4
    4. Molecular Formula: C8H13NO3
    5. Molecular Weight: 171.19372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101327-98-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 1-Methyl-2-oxopiperidine-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 1-Methyl-2-oxopiperidine-3-carboxylate(101327-98-4)
    11. EPA Substance Registry System: Methyl 1-Methyl-2-oxopiperidine-3-carboxylate(101327-98-4)

  • 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: 101327-98-4(Hazardous Substances Data)

101327-98-4 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex molecular structures, enhancing the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is employed as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can improve crop protection and yield.
Used in Organic Synthesis:
Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is used as a reagent in organic synthesis reactions, facilitating the formation of new compounds and contributing to the advancement of organic chemistry research and development.
It is crucial to handle Methyl 1-Methyl-2-oxopiperidine-3-carboxylate with care due to its potential harmful effects if ingested, inhaled, or absorbed through the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 101327-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101327-98:
(8*1)+(7*0)+(6*1)+(5*3)+(4*2)+(3*7)+(2*9)+(1*8)=84
84 % 10 = 4
So 101327-98-4 is a valid CAS Registry Number.

101327-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-?Piperidinecarboxylic acid, 1-?methyl-?2-?oxo-?, methyl ester

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

1.5 Emergency phone number

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

More Details:101327-98-4 SDS

101327-98-4Downstream Products

101327-98-4Relevant articles and documents

Bifunctional iminophosphorane superbases: Potent organocatalysts for enantio- and diastereoselective Michael addition reactions

Farley, Alistair J.M.,Jakubec, Pavol,Goldys, Anna M.,Dixon, Darren J.

, p. 5206 - 5212 (2018)

Bifunctional iminophosphorane (BIMP) organocatalysts catalyze the enantio- and diastereoselective Michael additions of high pKa cyclic malonamate ester pro-nucleophiles to nitroalkenes with reactivity profiles of up to 3 orders of magnitude greater than tertiary amine bifunctional Br?nsted base/(thio)urea organocatalysts. The unrivalled performance of the BIMPs allows reaction times of challenging reactions to be slashed from weeks to minutes and has enabled new flow chemistry applications using polystyrene-supported versions contained within a flow reactor.

α-HYDROXYLATION OF β-DICARBONYL COMPOUNDS

Andriamialiosa, R. Z.,Langlois, N.,Langlois, Y.

, p. 3563 - 3566 (2007/10/02)

Various β-dicarbonyl compounds can be hydroxylated as their silyl enol ethers by m-chloroperbenzoic acid (MCPBA).

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