58851-76-6

Basic information

• Product Name: 5,8-dihydronaphthalene-1,4-diyl diacetate
• CAS NO: 58851-76-6
• Molecular Formula: C₁₄H₁₄O₄
• Molecular Weight: 246.2586
• Mol File: 58851-76-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 385.6°C at 760 mmHg
• Flash Point: 194.8°C
• Density: 1.202g/cm³
• Vapor Pressure: 3.77E-06mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 5,8-dihydronaphthalene-1,4-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 5,8-dihydronaphthalene-1,4-diyl diacetate(58851-76-6)
• EPA Substance Registry System: 5,8-dihydronaphthalene-1,4-diyl diacetate(58851-76-6)

Safety Data

• Hazardous Substances Data: 58851-76-6(Hazardous Substances Data)

Upstream product

• 6271-40-5 4a,5,8,8a-tetrahydro-1,4-naphthoquinone 
• 108-24-7 acetic anhydride 
• 35043-92-6 cis-5,8,9,10-tetrahydronaphtho-1,4-quinone 
• 6295-28-9 5,8-dihydronaphthalene-1,4-dione 
• 3090-45-7 5,8-dihydro-1,4-naphthalenediol 
• 106-51-4 p-benzoquinone 

Downstream Products

• 5697-00-7 1,4-diacetoxynaphthalene 
• 7475-24-3 5,6,7,8-tetrahydronaphthalene-1,4-diacetate 
• 14569-45-0 5,8-diacetoxy-1,4-naphthoquinone 
• 1785-65-5 2-acetoxy-1,4-naphthoquinone 
• 58851-77-7 6-acetyloxy-1a,2,7,7a-tetrahydronaphtho[2,3-b]oxiren-3-yl acetate 
• 13623-10-4 5,6,7,8-tetrahydronaphthalene-1,4-diol 
• 571-60-8 1,4-Dihydroxynaphthalene 
• 41426-37-3 4-isopropyloxynaphth-1-ol 

Relevant articles and documents

Synthesis of anthracyclinone precursor: 5,12-dihydroxy-1,3,4- trihydronaphthacene-2,6,11-quinone

Two practical and efficient approaches for preparing large quantities of 5,12-dihydroxy-1,3,4-trihydronaphthacene-2,6,11-quinone 9 are described. Both synthetic approaches involve a simple route with a fewer number of steps and utilize readily available and inexpensive starting materials. Large-scale production of this precursor may prove to be useful for further research involving the synthesis of antineoplastic anthracyclines and development of their analogs with increased activity and decreased toxicity.