62952-40-3

Basic information

• Product Name: 1-Cyclohexene-1-carboxaldehyde, 3-oxo-
• CAS NO: 62952-40-3
• Molecular Formula: C7H8O2
• Molecular Weight: 124.139
• Mol File: 62952-40-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Cyclohexene-1-carboxaldehyde, 3-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexene-1-carboxaldehyde, 3-oxo-(62952-40-3)
• EPA Substance Registry System: 1-Cyclohexene-1-carboxaldehyde, 3-oxo-(62952-40-3)

Safety Data

• Hazardous Substances Data: 62952-40-3(Hazardous Substances Data)

Usage

Explanation

The molecular formula of 1-Cyclohexene-1-carboxaldehyde, 3-oxorepresents the number of carbon (C), hydrogen (H), and oxygen (O) atoms present in the compound.

Explanation

The compound features an aldehyde functional group (R-CHO) attached to the third carbon atom of a cyclohexene ring, which is a six-membered ring with alternating single and double bonds between carbon atoms.

Explanation

Due to its unique structure, 1-Cyclohexene-1-carboxaldehyde, 3-oxois used as a building block or intermediate in the synthesis of various organic compounds. It is also utilized in the creation of fragrances and flavorings for the food and cosmetic industries.
4. Antibacterial and antifungal properties

Explanation

The compound has been found to exhibit antibacterial and antifungal activities, which makes it a potential candidate for use in pharmaceutical applications, such as in the development of new drugs or treatments.

Explanation

1-Cyclohexene-1-carboxaldehyde, 3-oxois employed in various industrial processes, including the manufacturing of plastics, rubber, and pharmaceuticals, due to its versatile chemical properties and reactivity.

Explanation

The compound is soluble in organic solvents such as ethanol, acetone, and diethyl ether, which allows for its use in various chemical reactions and processes.

Explanation

1-Cyclohexene-1-carboxaldehyde, 3-oxois generally stable under normal temperature and pressure conditions, making it suitable for use in various applications without the need for special handling or storage requirements.

Explanation

As with many chemicals, 1-Cyclohexene-1-carboxaldehyde, 3-oxocan pose health risks if not handled properly. It may cause irritation to the eyes, skin, and respiratory system, and can be harmful if inhaled or absorbed through the skin. Proper safety measures should be taken when working with this compound.

Structure

Aldehyde with a carbonyl group on the third carbon of a cyclohexene ring

Applications

Synthesis of other organic compounds, production of fragrances and flavorings

Industrial uses

Production of plastics, rubber, and pharmaceuticals

Solubility

Soluble in organic solvents

Stability

Stable under normal conditions

Hazards

Potential irritant and harmful if inhaled or absorbed through the skin

Upstream product

• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 6749-63-9 3-hydroxy-1-methylenecyclohexane 
• 69814-26-2 3-oxocyclohexanecarbaldehyde 
• 76320-22-4 3-(hydroxymethyl)cyclohex-2-en-1-one 
• 58775-66-9 3-<(phenylthio)methyl>-2-cyclohexen-1-one 
• 675107-22-9 3-phenylsulfinylmethylcyclohex-2-en-1-one 
• 125991-67-5 3-Trimethylenedithiomethyl-2-cyclohexen-2-one 
• 201230-82-2 carbon monoxide 
• 56671-82-0 3-Iodocyclohex-2-enone 

Downstream Products

• 144918-16-1 3-Dimethoxymethyl-6-(1-hydroxy-1-methylethyl)-2-cyclohexen-1-one 
• 102574-06-1 (E)-3-Methyl-4-[3-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-cyclohex-2-en-(E)-ylidene]-but-2-enal 
• 102574-08-3 (Z)-3-Methyl-4-[3-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-cyclohex-2-en-(E)-ylidene]-but-2-enal 
• 102574-07-2 (E)-3-Methyl-4-[3-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-cyclohex-2-en-(Z)-ylidene]-but-2-enal 
• 102574-09-4 (Z)-3-Methyl-4-[3-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-cyclohex-2-en-(Z)-ylidene]-but-2-enal 
• 102586-39-0 [3-[(1E,3E)-2-Methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-dienyl]-cyclohex-2-en-(E)-ylidene]-acetaldehyde 
• 102574-05-0 [3-[(1E,3E)-2-Methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-dienyl]-cyclohex-2-en-(Z)-ylidene]-acetaldehyde 
• 102574-20-9 (E)-3-Methyl-4-[3-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-cyclohex-2-en-(E)-ylidene]-but-2-enenitrile 
• 102574-12-9 [3-[(1E,3E)-2-Methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-dienyl]-cyclohex-2-en-(E)-ylidene]-acetonitrile 
• 454442-10-5 3-[3-(cyano-ethylidene)-cyclohex-1-enyl]-2-methyl-acrylic acid ethyl ester 
• 454442-11-6 2-[3-(3-hydroxy-2-methyl-propenyl)-cyclohex-2-enylidene]-propionaldehyde 
• 454442-05-8 2-methyl-3-[3-(1-methyl-2-oxoethylidene)-cyclohex-1-enyl]-propenal 
• 675107-25-2 3-(tert-butyldimethylsiloxymethyl)-2-iodocyclohex-2-en-1-one 
• 675107-23-0 3-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohex-2-enol 

Relevant articles and documents

Synthetic approaches to phomactins: Novel oxidation of homoallylic alcohols using tetra-n-propylammonium perruthenate

Previous studies of a synthesis of phomactin A had resulted in the synthesis of a 15-methylenebicyclo[9.3.1]pentadecadiene. The next step in the synthesis was to be the epoxidation of this methylenecyclohexane that was hoped would lead to a 1-(hydroxymethyl)cyclohexene by rearrangement of the exocyclic epoxide, but the epoxidation was difficult to carry out regioselectively on advanced intermediates. However, oxidation of a 15-methylenebicyclo[9.3.1]pentadeca-3,7-dien-14-ol using tetra-n-propylammonium perruthenate and N-methylmorpholine-N-oxide led to conversion of this homoallylic alcohol into the corresponding 14-oxobicyclo[9.3.1]pentadeca-1(15),3,7-triene-15-carboxaldehyde in one step. Reduction of this using DIBAL-H gave a promising intermediate for a synthesis of a phomactin. The scope of this oxidation of homoallylic alcohols was briefly investigated.

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