71441-29-7

Basic information

• Product Name: N-ethyl-4-[(1E)-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl]benzamide
• CAS NO: 71441-29-7
• Molecular Formula: C₂₆H₃₃NO
• Molecular Weight: 375.5463
• Mol File: 71441-29-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 521.9°C at 760 mmHg
• Flash Point: 322.7°C
• Density: 1.006g/cm³
• Vapor Pressure: 5.43E-11mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: N-ethyl-4-[(1E)-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyl-4-[(1E)-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl]benzamide(71441-29-7)
• EPA Substance Registry System: N-ethyl-4-[(1E)-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl]benzamide(71441-29-7)

Safety Data

• Hazardous Substances Data: 71441-29-7(Hazardous Substances Data)

Upstream product

• 6287-86-1 p-ethoxycarbonylbenzaldehyde 
• 6683-46-1 1,1,4,4-Tetramethyl-1,2,3,4-tetrahydro-naphthalene 
• 78315-04-5 (E)-4-<2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-2-methylethenyl>benzoyl chloride 
• 75-04-7 ethylamine 
• 69251-25-8 5,6,7,8-tetrahydro-α,5,5,8,8-pentamethyl-2-naphthalene methanol 
• 69251-26-9 2-(bromoethyl)-5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene 
• 71441-09-3 AGN 190316 
• 71441-28-6 TTNPB 
• 69251-24-7 [1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-ethyl]-triphenylphosphonium bromide 
• 17610-21-8 1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)ethanone 

Relevant articles and documents

Arotinoids, a new class of highly active retinoids

The synthesis and biological activity of new aromatic retinoids are reported. The most active ones belong to a chemical class of compounds, which we have termed 'arotinoids'. For the compound p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl)]-benzoic acid ethyl ester, a therapeutic potency in the antipapilloma test was found which exceeds that of retinoic acid by a factor of 8000, while the concurrently observed toxic hypervitaminosis A effects are only increased by a factor of 800. The structural relationship of the arotinoids with retinoic acid is demonstrated; the arotinoids contain the retinoic acid carbon skeleton in a fixed cisoid geometric conformation.