1-Aminoanthracene

Base Information

• Chemical Name: 1-Aminoanthracene
• CAS No.: 610-49-1
• Molecular Formula: C14H11 N
• Molecular Weight: 193.248
• Hs Code.: 2921499090
• European Community (EC) Number: 210-225-8
• NSC Number: 60017
• UNII: 8H6056DWN2
• DSSTox Substance ID: DTXSID00209859
• Nikkaji Number: J3.649H
• Wikipedia: Anthramine
• Wikidata: Q4117196
• Metabolomics Workbench ID: 56388
• ChEMBL ID: CHEMBL82321
• Mol file: 610-49-1.mol

Synonyms:1-aminoanthracene

Chemical Property of 1-Aminoanthracene

Chemical Property:

• Vapor Pressure: 7.12E-07mmHg at 25°C
• Melting Point: 114-118 °C(lit.)
• Refractive Index: 1.5850 (estimate)
• Boiling Point: 408.2°C at 760 mmHg
• PKA: 4.21±0.30(Predicted)
• Flash Point: 224.4°C
• PSA: 26.02000
• Density: 1.208g/cm³
• LogP: 4.15640
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 193.089149355
• Heavy Atom Count: 15
• Complexity: 225

Purity/Quality:

98%,99%, ^*data from raw suppliers

1-Aminoanthracene ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Polycyclic Aromatic Hydrocarbons
• Canonical SMILES: C1=CC=C2C=C3C(=CC2=C1)C=CC=C3N

Technology Process of 1-Aminoanthracene

There total 9 articles about 1-Aminoanthracene 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: 92.0%

1-amino-9,10-anthracenedione (82-45-1) → 1-aminoanthracene (610-49-1)

Guidance literature:

With sodium hydroxide; zinc; at 85 ℃; for 24.5h; Inert atmosphere;

Reference yield: 84.2%

→ 1-aminoanthracene (610-49-1)

Guidance literature:

Reference yield:

acetamide (60-35-5) + 1-hydroxyanthracene (610-50-4) → 1-aminoanthracene (610-49-1)

Guidance literature:

upstream raw materials:

acetamide

1-hydroxyanthracene

9,10-dihydro-[1]anthrylamine

1-nitroanthraquinone

Downstream raw materials:

4-phenylazo-[1]anthrylamine

1-hydroxyanthracene

1,2,3,4-tetrahydroanthracene

1,2,3,4,5,6,7,8-octahydroanthracene

Refernces

• 1、 -. "Preparation method and application of anthryl hydrogen bond molecular folding material". Paragraph 0034-0036. . Retrieved 2019/11/20.
• 2、 Ikedu, Satomi,Nishimura, Yoshinobu,Arai, Tatsuo. "Kinetics of hydrogen bonding between anthracene urea derivatives and anions in the excited state". experimental part. p. 8227 - 8233. Retrieved 2011/09/20.