80825-32-7

Basic information

• Product Name: (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde
• Synonyms: (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde
• CAS NO: 80825-32-7
• Molecular Weight: 186.254
• Mol File: 80825-32-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde(80825-32-7)
• EPA Substance Registry System: (1R,2S)-2-phenylcyclohex-3-enecarbaldehyde(80825-32-7)

Safety Data

• Hazardous Substances Data: 80825-32-7(Hazardous Substances Data)

Upstream product

• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 107-02-8 acrolein 
• 100-52-7 benzaldehyde 
• 80735-94-0 1-Phenyl-3-buten-1-ol 

Downstream Products

• 36359-51-0 (+/-)-trans-2-phenylcyclohexanemethanol 
• 75649-64-8 (+/-)-trans-2-phenyl-cyclohex-3-enecarboxylic acid 
• 643-58-3 2-methylbiphenyl 
• 72316-03-1 (+/-)-cis-1-hydroxymethyl-2-phenyl-cyclohexene-⁽³⁾ 
• 36359-51-0 (+/-)-cis-2-phenylcyclohexanemethanol 
• 75649-64-8 (+/-)-cis-2-phenyl-cyclohexene-⁽³⁾-carboxylic acid-⁽¹⁾ 
• 98591-07-2 Acetyl-<2-phenyl-cyclohexen-(3)-yl>-carbinol 
• 93651-71-9 1-Acetoxy-1-(2-phenyl-cyclohex-3-enyl)-prop-2-in 
• 94327-45-4 1-(2-Phenyl-cyclohexyl)-propanol-⁽¹⁾ 
• 92581-09-4 Vinyl-<2-phenyl-cyclohexen-(3)-yl>-carbinol 
• 92650-77-6 1-<2-Phenyl-cyclohexyl>-propen-(1) 
• 80825-46-3 {6-[1-Ethoxy-meth-(E)-ylidene]-cyclohex-1-enyl}-benzene 
• 80825-41-8 {6-[1-Ethoxy-meth-(E)-ylidene]-cyclohex-2-enyl}-benzene 
• 80825-35-0 (6-Diethoxymethyl-cyclohex-2-enyl)-benzene 

Relevant articles and documents

Synthesis and anti-inflammatory activity of phenylbutenoid dimer analogs

Several phenylbutenoid dimer (PBD) analogs were synthesized and evaluated for their inhibitory activities against nitric oxide (NO) production and TNF-α release. The PBD analogs were synthesized via Diels - Alder and subsequent Schlosser reactions as key steps. Among the tested compounds, two analogs (8c, 8f) exhibited much stronger inhibitory activity against LPS-stimulated NO production and TNF-α release in RAW 264.7 cells than that of wogonin.