Sodium;naphthalene

Base Information

• Chemical Name: Sodium;naphthalene
• CAS No.: 3481-12-7
• Molecular Formula: C₁₀H₈*Na
• Molecular Weight: 151.163
• Mol file: 3481-12-7.mol

Synonyms:

Chemical Property of Sodium;naphthalene

Chemical Property:

• PSA: 0.00000
• LogP: 2.42090
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 151.05236954
• Heavy Atom Count: 11
• Complexity: 80.6

Purity/Quality:

99%, ^*data from raw suppliers

SODIUM NAPHTHALIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC=C2C=CC=CC2=C1.[Na+]

Technology Process of Sodium;naphthalene

There total 3 articles about Sodium;naphthalene 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:

naphthalene (91-20-3,71998-51-1,72931-45-4) → naphthalene radical anion sodium salt (3481-12-7,13269-57-3,116346-73-7)

Guidance literature:

With sodium; In tetrahydrofuran; for 24h;

DOI:10.1021/jo00150a003

Reference yield:

naphthalene (91-20-3,71998-51-1,72931-45-4) + sodium (7440-23-5) → naphthalene radical anion sodium salt (3481-12-7,13269-57-3,116346-73-7)

Guidance literature:

In tetrahydrofuran; Inert atmosphere; Schlenk technique;

DOI:10.1021/ic301675t

Reference yield:

naphthalene (91-20-3,71998-51-1,72931-45-4) → naphthalene radical anion sodium salt (3481-12-7,13269-57-3,116346-73-7)

Guidance literature:

In tetrahydrofuran; for 3h; Ambient temperature;

upstream raw materials:

naphthalene

sodium

Downstream raw materials:

sodium formate

naphthalene

Isobutane

2,2-dimethyl-propanol-1

Refernces

• 1、 Sartor, Steven M.,McCarthy, Blaine G.,Pearson, Ryan M.,Miyake, Garret M.,Damrauer, Niels H.. "Exploiting Charge-Transfer States for Maximizing Intersystem Crossing Yields in Organic Photoredox Catalysts". supporting information. p. 4778 - 4781. Retrieved 2018/04/17.
• 2、 Mondal, Pravat,Argade, Narshinha P.. "Formal Synthesis of Bioactive Indole Alkaloids Eburnamonine, Eburnaminol, and Vindeburnol". . p. 1849 - 1856. Retrieved 2017/04/06.