Naphthalene-1-carboxamidine

Base Information

• Chemical Name: Naphthalene-1-carboxamidine
• CAS No.: 14805-64-2
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.214
• Hs Code.: 2925290090
• DSSTox Substance ID: DTXSID20486483
• Wikidata: Q82327488
• Mol file: 14805-64-2.mol

Synonyms:NAPHTHALENE-1-CARBOXAMIDINE;14805-64-2;1-NAPHTHIMIDAMIDE;naphthalene-1-carboximidamide;1-naphthalenecarboximidamide;naphthamidine;ETHYL3-OXODECANOATE;SCHEMBL49654;DTXSID20486483;MELCHBVBYGSSOC-UHFFFAOYSA-N;MFCD04114413;AB18265;CS-0446989;FT-0734628;F18397;A808730

Chemical Property of Naphthalene-1-carboxamidine

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 154 °C
• Refractive Index: 1.63
• Boiling Point: 328.457 °C at 760 mmHg
• PKA: 11.60±0.30(Predicted)
• Flash Point: 152.445 °C
• PSA: 49.87000
• Density: 1.165 g/cm³
• LogP: 2.92390
• Storage Temp.: 2-8°C
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 170.084398327
• Heavy Atom Count: 13
• Complexity: 200

Purity/Quality:

97% ^*data from raw suppliers

Naphthalene-1-carboxamidine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C=CC=C2C(=N)N

Technology Process of Naphthalene-1-carboxamidine

There total 7 articles about Naphthalene-1-carboxamidine 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:

→ α-Naphthamidin (14805-64-2)

Guidance literature:

With methanol; nickel; at 60 ℃; under 22065.2 Torr; Hydrogenation;

Reference yield:

C13H13NO*BF4(1-)*H(1+) → α-Naphthamidin (14805-64-2)

Guidance literature:

With ammonia; In ethanol;

DOI:10.1021/jo01268a093

Reference yield:

→ α-Naphthamidin (14805-64-2)

Guidance literature:

With ammonia; aniline; at 140 ℃;

DOI:10.1039/jr9490000449

upstream raw materials:

hydrogen iodide

ammonium benzenesulfonate

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