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Cyclohexanecarboxylic acid, 3-methyl-2-oxo-, ethyl ester, also known as ethyl 3-methyl-2-oxocyclohexanecarboxylate, is an organic compound with the chemical formula C10H16O3. It is a colorless liquid with a molecular weight of 184.23 g/mol. This ester is derived from cyclohexanecarboxylic acid, featuring a methyl group at the 3-position and an oxo group at the 2-position. The ethyl ester is formed by the esterification of the carboxylic acid group with ethanol. It is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can undergo further chemical transformations, making it a valuable building block in organic synthesis.

5183-61-9

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5183-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5183-61-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5183-61:
(6*5)+(5*1)+(4*8)+(3*3)+(2*6)+(1*1)=89
89 % 10 = 9
So 5183-61-9 is a valid CAS Registry Number.

5183-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Epoxy-4,5 hexene-2 (E) oate de methyle

1.2 Other means of identification

Product number -
Other names methyl (E)-4,5-epoxyhex-2-enoate

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:5183-61-9 SDS

5183-61-9Relevant academic research and scientific papers

Oxidative dearomatization/intramolecular Diels-Alder cycloaddition cascade for the syntheses of (±)-atisine and (±)-isoazitine

Liu, Xiao-Yu,Cheng, Hang,Li, Xiao-Huan,Chen, Qiao-Hong,Xu, Liang,Wang, Feng-Peng

, p. 1411 - 1417 (2012)

A convergent and efficient formal synthesis of (±)-atisine has been accomplished. The synthetic strategy is to efficiently construct the bicyclo[2.2.2]octane ring moiety by an oxidative dearomatization/intramolecular Diels-Alder cycloaddition cascade. The first total synthesis of another atisine-type C20-diterpenoid alkaloid, (±)-isoazitine, has also been achieved employing the same strategy.

Dynamic Kinetic Resolution of I-Substituted Cyclic β-Ketoesters via Asymmetric Hydrogenation: Constructing Chiral Cyclic β-Hydroxyesters with Three Contiguous Stereocenters

Yang, Dan,Wu, Xiong,Zheng, Xiao-Jie,Xie, Jian-Hua,Zhou, Qi-Lin

supporting information, p. 5153 - 5157 (2021/07/20)

An efficient asymmetric hydrogenation of racemic I-substituted cyclic β-ketoesters via dynamic kinetic resolution to provide chiral cyclic β-hydroxy esters with three contiguous stereocenters is reported. Using a chiral spiro iridium catalyst (R)-5 (Ir-SpiroSAP), a series of racemic I-Aryl/alkyl substituted cyclic β-ketoesters were hydrogenated to the corresponding chiral cyclic β-hydroxy esters in high yields (84-97%) with good to excellent enantioselectivities (69->99% ee) and cis,cis-selectivities (up to >99:1).

METHODS OF TREATING DISORDER

-

Page/Page column 29, (2008/06/13)

Compound of formula (I) and methods of treating disorders by administering a compound of formula (I) are described herein. Examples of disorders include neoplastic disorders, fat-cell related disorders, neurodegenerative disorders, and metabolic disorders

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