606122-74-1

Basic information

• Product Name: (4-oxocyclohexyl)acetaldehyde
• Synonyms: (4-oxocyclohexyl)acetaldehyde
• CAS NO: 606122-74-1
• Molecular Weight: 140.182
• Mol File: 606122-74-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4-oxocyclohexyl)acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (4-oxocyclohexyl)acetaldehyde(606122-74-1)
• EPA Substance Registry System: (4-oxocyclohexyl)acetaldehyde(606122-74-1)

Safety Data

• Hazardous Substances Data: 606122-74-1(Hazardous Substances Data)

Upstream product

• 90199-14-7 2-(4-Keto-cyclohexen-⁽¹⁾-yl)-ethylalkohol 
• 135761-76-1 2-(1,4-dioxaspiro[4.5]decan-8-yl)ethanol 
• 62141-26-8 ethyl 1,4-dioxaspiro[4.5]dec-8-ylacetate 
• 51656-91-8 ethyl 1,4-dioxaspiro[4,5]dec-8-ylideneacetate 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 32863-01-7 4-(2-hydroxyethyl)cyclohexan-1-one 

Downstream Products

• 1357255-94-7 2-(4-hydroxycyclohexyl)acetaldehyde 
• 141223-48-5 4-<(2Z)-3-(methoxycarbonyl)-2-propenyl>cyclohexan-1-one 
• 141223-49-6 4-<(2E)-3-(methoxycarbonyl)-2-propenyl>cyclohexan-1-one 

Relevant articles and documents

Chemoenzymatic preparation of functionalized bicyclo[3.2.1]octenone and practical utilization

A practical route for the synthesis of both enantiomers of a functionalized bicyclo[3.2.1]octenone, which is potentially useful as a versatile chiral building block, has been developed from 1,4-cyclohexanedione monoethylene acetal by employing proline-cat

Synthesis of polycyclic cyclobutane derivatives by tandem intramolecular Michael-aldol reaction under two complementary conditions: TBDMSOTf-Et3N and TMSI-(TMS)2NH

The treatment of αβ-unsaturated esters having a ketone function at an appropriate position with either TBDMSOTf in the presence of Et3N or TMSI in the presence of (TMS)2NH provided, via a tandem intramolecular Michael-aldol reaction sequence, several different types of cyclobutane derivatives. The two reaction conditions were complementary. Tricyclo[4.2.1.03,8]nonanes 34 and 55, tricyclo[5.1.104,8]nonane 40, tricyclo[5.4.0.03,7]undecane 51, tetracyclo[5.4.0.03,7.09,11]undecane 45, and the bicyclo[3.2.0]heptanes 56, 57, and 58, which have structures either partially or completely similar to those of endiandric acids A (1a), B (1b), and C (2), trihydroxydecipiadiene (3), lintenone (4), italicene (5), and filifolone (6), were stereoselectively synthesized by the tandem reaction.