1271910-76-9

Basic information

• Product Name: 4-(3,4-dimethoxyphenyl)-N-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)butanamide
• Synonyms: 4-(3,4-dimethoxyphenyl)-N-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)butanamide
• CAS NO: 1271910-76-9
• Molecular Weight: 423.596
• Mol File: 1271910-76-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(3,4-dimethoxyphenyl)-N-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3,4-dimethoxyphenyl)-N-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)butanamide(1271910-76-9)
• EPA Substance Registry System: 4-(3,4-dimethoxyphenyl)-N-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)butanamide(1271910-76-9)

Safety Data

• Hazardous Substances Data: 1271910-76-9(Hazardous Substances Data)

Upstream product

• 13575-74-1 4-(3,4-dimethoxyphenyl)butanoic acid 
• 116233-17-1 3-methyl-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylamine 
• 110-03-2 2,5-dimethyl-2,5-hexanediol 
• 6223-78-5 2,5-dichloro-2,5-dimethyl hexane 
• 6683-48-3 1,1,4,4,6-pentamethyl-1,2,3,4-tetrahydronaphthalene 
• 116233-16-0 1,2,3,4-tetrahydro-1,1,4,4,6-pentamethyl-7-nitronaphthalene 

Relevant articles and documents

Synthesis and effects of some novel tetrahydronaphthalene derivatives on proliferation and nitric oxide production in lipopolysaccharide activated Raw 264.7 macrophages

In this study, novel N-(3,5,5,8,8-pentamethyl-5,6,7,8- tetrahydronaphthalene-2-yl)-carboxamide (6-15) and 5,5,8,8-tetramethyl-5,6,7,8- tetrahydronaphthalene-2-carboxamide (16-32) derivatives were synthesized and their in vitro effects at 5 μM and 50 μM concentrations on proliferation and nitric oxide (NO) production in lipopolysaccharide (LPS) activated RAW 264.7 macrophage cells were determined. Compounds 12, 17, 24 and 26 were found to decrease nitrite levels in a dose-dependent manner in LPS-activated cells. At the tested concentrations, these compounds did not exhibit cytotoxic effects. Interestingly, compound 27 which contains nitroxide free radical was the most active compound in this series showing 59.2% nitrite inhibition in LPS-activated macrophage cells.