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(1R,4R)-4-(ethoxycarbonyl)cyclohexanecarboxylic acid is a chiral organic compound characterized by a cyclohexane ring with a carboxylic acid group and an ethyl ester functional group. Its (1R,4R) designation signifies the specific arrangement of the ethyl ester group on the chiral carbons, which is crucial for its potential applications in various fields.

15177-66-9

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15177-66-9 Usage

Uses

Used in Organic Synthesis:
(1R,4R)-4-(ethoxycarbonyl)cyclohexanecarboxylic acid is used as a building block in organic synthesis for the preparation of various pharmaceuticals and other organic compounds. Its unique structure and functional groups make it a valuable intermediate in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1R,4R)-4-(ethoxycarbonyl)cyclohexanecarboxylic acid is used as a key intermediate in the synthesis of specific drug molecules. Its chiral nature allows for the development of enantiomerically pure compounds, which can exhibit different biological activities and reduce potential side effects.
Used in Materials Science:
(1R,4R)-4-(ethoxycarbonyl)cyclohexanecarboxylic acid has potential applications in the development of new materials, such as polymers and coatings. Its carboxylic acid and ethyl ester functional groups can participate in various polymerization and cross-linking reactions, leading to the creation of novel materials with unique properties.
Used in Chemical Reactions:
The ethyl ester group of (1R,4R)-4-(ethoxycarbonyl)cyclohexanecarboxylic acid can undergo hydrolysis to form the corresponding carboxylic acid, which can then participate in further chemical reactions. This property allows for the modification and functionalization of the compound, expanding its utility in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 15177-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,7 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15177-66:
(7*1)+(6*5)+(5*1)+(4*7)+(3*7)+(2*6)+(1*6)=109
109 % 10 = 9
So 15177-66-9 is a valid CAS Registry Number.

15177-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxycarbonylcyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names Cyclohexan-trans-1.4-dicarbonsaeure-monoethylester

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:15177-66-9 SDS

15177-66-9Relevant academic research and scientific papers

Trans -4 - amino - cyclohexyl carboxylic acid ethyl ester hydrochloride of preparation method (by machine translation)

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Paragraph 0032; 0034; 0037; 0039; 0042; 0044, (2019/02/13)

The invention discloses a method for trans - 4 - amino - cyclohexyl carboxylic acid ethyl ester hydrochloride of the preparation method, which belongs to the field of organic chemistry, the method is to trans - 1, 4 - cyclohexyl dicarboxylic acid as a sta

Synthesis of 1,4-Cyclohexanedimethanol, 1,4-Cyclohexanedicarboxylic Acid and 1,2-Cyclohexanedicarboxylates from Formaldehyde, Crotonaldehyde and Acrylate/Fumarate

Hu, Yancheng,Zhao, Zhitong,Liu, Yanting,Li, Guangyi,Wang, Aiqin,Cong, Yu,Zhang, Tao,Wang, Feng,Li, Ning

, p. 6901 - 6905 (2018/06/04)

Valuable polyester monomers and plasticizers—1,4-cyclohexanedimethanol (CHDM), 1,4-cyclohexanedicarboxylic acid (CHDA), and 1,2-cyclohexanedicarboxylates—have been prepared by a new strategy. The synthetic processes involve a proline-catalyzed formal [3+1+2] cycloaddition of formaldehyde, crotonaldehyde, and acrylate (or fumarate). CHDM is produced after a subsequent hydrogenation step over a commercially available Cu/Zn/Al catalyst and a one-pot hydrogenation/oxidation/hydrolysis process yields CHDA, whereas 1,2-cyclohexanedicarboxylate is obtained by a Pd/C-catalyzed tandem decarbonylation/hydrogenation step.

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