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66405-41-2

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66405-41-2 Usage

General Description

(4-OXO-CYCLOHEXYL)-ACETIC ACID METHYL ESTER is a chemical compound with the molecular formula C9H14O3. It is a methyl ester derivative of (4-oxo-cyclohexyl)-acetic acid, which is a cyclohexanecarboxylic acid derivative. (4-OXO-CYCLOHEXYL)-ACETIC ACID METHYL ESTER is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a building block in organic synthesis. (4-OXO-CYCLOHEXYL)-ACETIC ACID METHYL ESTER has potential applications in the pharmaceutical industry due to its ability to serve as a precursor for the synthesis of bioactive molecules. However, it is important to handle this compound with care as it may pose health risks and should be used in accordance with safe handling procedures and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 66405-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66405-41:
(7*6)+(6*6)+(5*4)+(4*0)+(3*5)+(2*4)+(1*1)=122
122 % 10 = 2
So 66405-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O3/c1-12-9(11)6-7-2-4-8(10)5-3-7/h7H,2-6H2,1H3

66405-41-2SDS

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 2-(4-oxocyclohexyl)acetate

1.2 Other means of identification

Product number -
Other names (4-Keto-cyclohexyl)essigsaeuremethylester

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:66405-41-2 SDS

66405-41-2Relevant articles and documents

A practical synthesis of a potent and selective diacylglycerol acyltransferase-1 (DGAT-1) inhibitor

Shin, Youngsook,Bergeron, Philippe,Fox, Brian M.,Kayser, Frank,McGee, Lawrence R.,McKendry, Sharon,McMinn, Dustin L.,Labelle, Marc,Cushing, Timothy D.

, p. 3047 - 3058 (2014)

A practical synthesis of a potent, selective, and orally efficacious diacylglycerol acyltransferase-1 (DGAT-1) inhibitor, is described. This synthesis is suitable for multi-kilogram scale with high regioselectivity and stereoselectivity. The synthesis inv

Continuous Synthesis of Aryl Amines from Phenols Utilizing Integrated Packed-Bed Flow Systems

Ichitsuka, Tomohiro,Kobayashi, Shū,Koumura, Nagatoshi,Sato, Kazuhiko,Takahashi, Ikko

supporting information, p. 15891 - 15896 (2020/07/13)

Aryl amines are important pharmaceutical intermediates among other numerous applications. Herein, an environmentally benign route and novel approach to aryl amine synthesis using dehydrative amination of phenols with amines and styrene under continuous-flow conditions was developed. Inexpensive and readily available phenols were efficiently converted into the corresponding aryl amines, with small amounts of easily removable co-products (i.e., H2O and alkanes), in multistep continuous-flow reactors in the presence of heterogeneous Pd catalysts. The high product selectivity and functional-group tolerance of this method allowed aryl amines with diverse functional groups to be selectively obtained in high yields over a continuous operation time of one week.

A biocatalytic/reductive etherification approach to substituted piperidinyl ethers

Kuethe, Jeffrey T.,Janey, Jacob M.,Truppo, Matthew,Arredondo, Juan,Li, Tao,Yong, Kelvin,He, Shuwen

, p. 4563 - 4570 (2014/06/10)

A synthetically useful protocol has been developed for the preparation of highly functionalized piperidinyl ethers. Biocatalytic reduction of cyclhexanones 7, 10, and 14 allows for the preparation of both cis- and trans diastereomers with an extremely high degree of stereochemical control. Reductive etherification of the corresponding trimethylsilylethers with 1-(benzyloxycarbonyl)-4-piperidinone 17 in the presence of triethylsilane and catalytic TMSO-Tf provides the desired piperidinyl ethers in good to excellent yields. Finally hygrogenolysis of the nitrogen protecting group leads to piperidinyl ethers in near quantitative yields. Application of the methodology to a range of piperidinyl ethers, including the core scaffolds of diphenylpyraline and ebastine, is also described.

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