6038-12-6 Usage
Description
(E)-Cyclooct-1-enecarbaldehyde, also known as 1-cyclooctene-1-carbaldehyde, is a chemical compound characterized by its molecular formula C8H12O. It features an aldehyde group and a cyclic structure with a carbon-carbon double bond in the cyclooctene ring. (E)-Cyclooct-1-enecarbaldehyde is recognized for its strong, fruity odor and is utilized in various industries due to its versatile chemical properties.
Uses
Used in Organic Synthesis:
(E)-Cyclooct-1-enecarbaldehyde is used as a building block in organic synthesis for the creation of diverse organic molecules. Its cyclic structure and reactive aldehyde group make it a valuable component in the synthesis of complex organic compounds.
Used in Fragrance and Flavor Industry:
(E)-Cyclooct-1-enecarbaldehyde is used as a key component in the production of fragrance and flavor compounds. Its strong, fruity odor makes it an ideal candidate for enhancing the scent and taste of various products in this industry.
Used in Pharmaceutical Manufacturing:
(E)-Cyclooct-1-enecarbaldehyde is employed in the manufacturing of pharmaceuticals, where its unique chemical structure contributes to the development of new drugs and medicinal compounds.
Used in Agrochemicals Production:
(E)-Cyclooct-1-enecarbaldehyde is also utilized in the production of agrochemicals, where it can be a part of the synthesis process for creating pesticides, herbicides, and other agricultural chemicals.
Used as a Flavoring Agent in Food Products:
Due to its strong, fruity odor, (E)-Cyclooct-1-enecarbaldehyde is often used as a flavoring agent in the food industry to add a pleasant taste and aroma to various food products.
Safety Precautions:
It is important to handle (E)-Cyclooct-1-enecarbaldehyde with care, as it may be irritating to the skin, eyes, and respiratory tract. Proper safety measures should be taken during its use and storage to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6038-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6038-12:
(6*6)+(5*0)+(4*3)+(3*8)+(2*1)+(1*2)=76
76 % 10 = 6
So 6038-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O/c10-8-9-6-4-2-1-3-5-7-9/h6,8H,1-5,7H2/b9-6+
6038-12-6Relevant articles and documents
-
Cope,A.C.,Burton,P.E.
, p. 5439 - 5445 (1960)
-
Pd-Catalyzed Carbonylation of Vinyl Triflates to Afford α,β-Unsaturated Aldehydes, Esters, and Amides under Mild Conditions
Zhang, Shaoke,Neumann, Helfried,Beller, Matthias
, p. 3528 - 3532 (2019/05/24)
An efficient and general protocol for the synthesis of α,β-unsaturated aldehydes, esters, and amides via carbonylation of vinyl triflates including derivatives of camphor, ketoisophorone, verbenone, and pulegone was developed. Crucial for these transformations is the use of a specific palladium catalyst containing a pyridyl-substituted dtbpx-type ligand. This procedure also allows for an easy access of dicarbonylated products from the corresponding ketones.
Palladium catalysts for the formylation of vinyl triflates to form α,β-unsaturated aldehydes
Neumann, Helfried,Sergeev, Alexey,Beller, Matthias
scheme or table, p. 4887 - 4891 (2009/02/08)
(Chemical Equation Presented) What a gas! Synthesis gas is the formylating agent in the efficient one-step title transformation promoted by a palladium catalyst with the bidentate ligand 1,2-bis(di-1-adamantylphosphinomethyl)benzene (see scheme). This method enables the conversion of six-to eight-membered-ring triflates into α,β-unsaturated aldehydes and the introduction of a formyl group into derivatives of elaborate natural compounds. Tf = trifluoromethanesulfonyl.
