1,2-Dihydro-1,5,8-trimethylnaphthalene

Base Information

• Chemical Name: 1,2-Dihydro-1,5,8-trimethylnaphthalene
• CAS No.: 4506-36-9
• Molecular Formula: C13H16
• Molecular Weight: 172.27
• Hs Code.: 2902909090
• UNII: Y6D44B0088
• Nikkaji Number: J113.377B
• Mol file: 4506-36-9.mol

Synonyms:4506-36-9;1,5,8-Trimethyl-1,2-dihydronaphthalene;1,2-DIHYDRO-1,5,8-TRIMETHYLNAPHTHALENE;1,4,5-TRIMETHYL-5,6-DIHYDRONAPHTHALENE;Naphthalene, 1,2-dihydro-1,5,8-trimethyl-;Y6D44B0088;UNII-Y6D44B0088;1,5,8-Trimethyl-1,2-dihydronaphthalene #

Chemical Property of 1,2-Dihydro-1,5,8-trimethylnaphthalene

Chemical Property:

• Vapor Pressure: 0.0148mmHg at 25°C
• Boiling Point: 265.7°Cat760mmHg
• Flash Point: 110.2°C
• PSA: 0.00000
• Density: 0.946g/cm³
• LogP: 3.82380
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 172.125200510
• Heavy Atom Count: 13
• Complexity: 204

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1CC=CC2=C(C=CC(=C12)C)C

Technology Process of 1,2-Dihydro-1,5,8-trimethylnaphthalene

There total 2 articles about 1,2-Dihydro-1,5,8-trimethylnaphthalene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4,5,8-Trimethyl-1,2,3,4-tetrahydro-[1]naphthol (66324-66-1) → 1,5,8-trimethyl-1,2-dihydronaphthalene (4506-36-9)

Guidance literature:

With iodine;

DOI:10.1021/ja01130a032

Reference yield:

1,4,5-trimethylnaphthalene (2131-41-1) → 1,5,8-trimethyl-1,2-dihydronaphthalene (4506-36-9)

Guidance literature:

With ammonia; sodium; In diethyl ether;

Reference yield:

1,5,8-trimethyl-1,2-dihydronaphthalene (4506-36-9) → 1,4,5-trimethylnaphthalene (2131-41-1)

Guidance literature:

With palladium on activated charcoal;

DOI:10.1021/ja01130a032

upstream raw materials:

4,5,8-Trimethyl-1,2,3,4-tetrahydro-[1]naphthol

1,4,5-trimethylnaphthalene

Downstream raw materials:

1,4,5-trimethylnaphthalene