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2-Cyclopentene-1-carboxylic acid, 4-oxo-, methyl ester (9CI) is a chemical compound characterized by the molecular formula C8H10O3. It is a methyl ester derivative of 2-cyclopentene-1-carboxylic acid, 4-oxo-, which is a cyclic unsaturated carboxylic acid. 2-Cyclopentene-1-carboxylicacid,4-oxo-,methylester(9CI) is known for its diverse industrial and pharmaceutical applications, including its role as a building block in organic synthesis and as a precursor for the production of other chemical compounds. Due to its potential hazards, it is crucial to handle this chemical with care and adhere to proper safety procedures.

59895-12-4

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59895-12-4 Usage

Uses

Used in Organic Synthesis:
2-Cyclopentene-1-carboxylic acid, 4-oxo-, methyl ester (9CI) is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for the formation of new molecules through chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyclopentene-1-carboxylic acid, 4-oxo-, methyl ester (9CI) serves as a precursor for the production of other chemical compounds. Its versatile structure enables the development of new drugs and therapeutic agents, contributing to the advancement of medicine and healthcare.
Used in Chemical Production:
2-Cyclopentene-1-carboxylic acid, 4-oxo-, methyl ester (9CI) is also utilized in the production of various chemical compounds for different industries. Its role as a precursor allows for the synthesis of compounds used in materials science, coatings, and other applications, further expanding its utility in the chemical industry.
Safety Precautions:
Due to the potential hazards associated with 2-Cyclopentene-1-carboxylic acid, 4-oxo-, methyl ester (9CI), it is essential to handle this chemical with caution. Proper safety procedures, including the use of personal protective equipment, should be followed to minimize risks and ensure the safe handling and storage of 2-Cyclopentene-1-carboxylicacid,4-oxo-,methylester(9CI).

Check Digit Verification of cas no

The CAS Registry Mumber 59895-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,9 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59895-12:
(7*5)+(6*9)+(5*8)+(4*9)+(3*5)+(2*1)+(1*2)=184
184 % 10 = 4
So 59895-12-4 is a valid CAS Registry Number.

59895-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-oxocyclopent-2-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 4-oxocyclopent-2-enecarboxylate

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:59895-12-4 SDS

59895-12-4Downstream Products

59895-12-4Relevant academic research and scientific papers

Photoinduced Rearrangement of Dienones and Santonin Rerouted by Amines

Zhang, Zhipeng,Ratnikov, Maxim,Spraggon, Glen,Alper, Phil B.

, p. 904 - 908 (2018)

The photoinduced rearrangement pathways of simple 2,5-dienones and the natural product santonin were found to be effectively rerouted by amines, giving rise to unprecedented products. Either cis olefins or cyclobutenes were obtained from 4,4-disubstituted 2,5-dienone upon irradiation (365 nm) in the presence of various amines depending on the solvent. Previously undescribed [4.4.0] and [5.3.0] fused-ring-containing products were obtained when santonin was irradiated (365 nm) in the presence of methylamine. The amines present in these reactions were incorporated into the products by means of amide-group formation.

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