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1H-Pyrrole-1-carboxylic acid, 2,3-dihydro-, ethyl ester (9CI) is a pyrrole derivative, a class of heterocyclic organic compounds. This colorless liquid possesses a fruity odor and is widely recognized for its versatility in chemical reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and various organic compounds. Its applications extend to the preparation of perfumes and flavorings, highlighting its significance in both the chemical and fragrance industries.

68471-56-7

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68471-56-7 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrrole-1-carboxylic acid, 2,3-dihydro-, ethyl ester (9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its ability to participate in various chemical reactions, contributing to the development of new medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-Pyrrole-1-carboxylic acid, 2,3-dihydro-, ethyl ester (9CI) serves as an essential component in the production of agrochemicals, playing a crucial role in the synthesis of compounds that aid in crop protection and enhancement.
Used in Perfume Industry:
This pyrrole derivative is utilized as a raw material in the preparation of perfumes, capitalizing on its fruity odor to create unique and appealing fragrances.
Used in Flavoring Industry:
1H-Pyrrole-1-carboxylic acid, 2,3-dihydro-, ethyl ester (9CI) is employed in the creation of flavorings, where its fruity scent adds depth and complexity to various food and beverage products.
Used in Research and Development:
In the realm of scientific research and development, this chemical compound is harnessed for its potential to undergo a range of chemical reactions, facilitating the exploration and creation of novel chemical entities.
It is crucial to handle 1H-Pyrrole-1-carboxylic acid, 2,3-dihydro-, ethyl ester (9CI) with care due to its potential health hazards, ensuring proper safety measures are in place throughout its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 68471-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,7 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68471-56:
(7*6)+(6*8)+(5*4)+(4*7)+(3*1)+(2*5)+(1*6)=157
157 % 10 = 7
So 68471-56-7 is a valid CAS Registry Number.

68471-56-7SDS

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 2,3-dihydro-1H-pyrrole-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-ethoxycarbonyl-2,3-dihydropyrrole

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:68471-56-7 SDS

68471-56-7Relevant academic research and scientific papers

Extensive substrate profiling of cyclopentadecanone monooxygenase as Baeyer-Villiger biocatalyst reveals novel regiodivergent oxidations

Fink, Michael J.,Fischer, Thomas C.,Rudroff, Florian,Dudek, Hanna,Fraaije, Marco W.,Mihovilovic, Marko D.

, p. 9 - 16 (2012/02/05)

Cyclopentadecanone monooxygenase (CPDMO) is one of the latest additions to the established library of Baeyer-Villiger monooxygenases. Desymmetrizations of substituted cyclobutanones and -hexanones as well as kinetic resolutions of racemic cycloketones are efficiently catalyzed by CPDMO. Moreover the enzyme shows unprecedented preference in regiodivergent oxidations of terpenones and the bicyclic Geissman-Waiss lactone precursor giving access to the optical antipode of retronecine and other pyrrolizidine alkaloids.

An Expedient Synthesis of N-Acceptor-Substituted 2,3-Dihydropyrrols from the Corresponding 2-Pyrrolidinones

Bach, Thorsten,Brummerhop, Harm

, p. 312 - 315 (2007/10/03)

The title compounds 1 were prepared from the corresponding N-acceptor substituted 2-methoxypyrrolidines 3 by elimination with trimethylsilyl trifluoromethanesulfonate (TMSOTf) and N,N-di-iso-propyl ethyl amine (6 exampies, 57-84% yield). The enantiomerica

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