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101327-98-4

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101327-98-4 Usage

General Description

Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is a chemical compound with the molecular formula C8H13NO3. It is a derivative of piperidine and contains a methyl ester group. Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It can also be used as a reagent in organic synthesis reactions. Methyl 1-Methyl-2-oxopiperidine-3-carboxylate is a white, crystalline solid with a molecular weight of 171.19 g/mol. It is important to handle this compound with care, as it may be harmful 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.

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