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(1r,4r)-Ethyl 4-formylcyclohexanecarboxylate is an organic chemical compound with a decomposable structure. It is characterized by its chemical formula C11H16O3 and a molar mass of 196.238g/mol. (1r,4r)-ethyl 4-formylcyclohexanecarboxylate belongs to the esters group and features a cyclohexane ring attached to a carboxylic ester function and an aldehyde group. It is typically used in the production of other useful chemicals or substances in various industrial applications. Proper safety guidelines should be followed for handling and storage to minimize health and environmental risks.

104802-53-1

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104802-53-1 Usage

Uses

Used in Chemical Production:
(1r,4r)-Ethyl 4-formylcyclohexanecarboxylate is used as an intermediate in the synthesis of various chemicals for industrial applications. Its unique structure allows for the creation of a wide range of products, making it a valuable component in chemical manufacturing processes.
Used in Pharmaceutical Industry:
(1r,4r)-Ethyl 4-formylcyclohexanecarboxylate is used as a building block in the development of pharmaceutical compounds. Its versatile structure can be incorporated into drug molecules, potentially leading to the discovery of new medications with improved efficacy and reduced side effects.
Used in Material Science:
(1r,4r)-Ethyl 4-formylcyclohexanecarboxylate is used as a component in the formulation of advanced materials, such as polymers and composites. Its incorporation can enhance the properties of these materials, leading to improved performance in various applications, including electronics, automotive, and aerospace industries.

Check Digit Verification of cas no

The CAS Registry Mumber 104802-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104802-53:
(8*1)+(7*0)+(6*4)+(5*8)+(4*0)+(3*2)+(2*5)+(1*3)=91
91 % 10 = 1
So 104802-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O3/c1-2-13-10(12)9-5-3-8(7-11)4-6-9/h7-9H,2-6H2,1H3

104802-53-1SDS

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 (1R,4R)-Ethyl 4-formylcyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-formylcyclohexane-1-carboxylate

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:104802-53-1 SDS

104802-53-1Upstream product

104802-53-1Relevant academic research and scientific papers

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

supporting information, 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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