1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl-

Base Information

• Chemical Name: 1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl-
• CAS No.: 54517-97-4
• Molecular Formula: C15H20N2O2S
• Molecular Weight: 292.402
• DSSTox Substance ID: DTXSID70480698
• Nikkaji Number: J450.807F
• Wikidata: Q82315673

Synonyms:54517-97-4;N-propyldansylamine;1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl-;SCHEMBL10002025;DTXSID70480698

Chemical Property of 1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl-

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 292.12454906
• Heavy Atom Count: 20
• Complexity: 403

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCNS(=O)(=O)C1=CC=CC2=C1C=CC=C2N(C)C

Technology Process of 1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl-

There total 1 articles about 1-Naphthalenesulfonamide, 5-(dimethylamino)-N-propyl- 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:

propylamine (107-10-8,42939-71-9) + 5-(dimethylamino)naphth-1-ylsulfonyl chloride (605-65-2) + 2-(N-tert-butoxycarbonylamino)ethanol (26690-80-2) + 3-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-2-(4-triisopropylsilanyloxy-phenyl)-benzo[b]thiophen-6-ol → 5-dimethylaminonaphthalene-1-sulfonic acid N-(propyl)amide (54517-97-4) + 5-dimethylamino-naphthalene-1-sulfonic acid [2-(4-{6-hydroxy-3-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-benzo[b]thiophen-2-yl}-phenoxy)-ethyl]-amide

Guidance literature:

Multistep reaction;

DOI:10.1016/S0040-4020(99)00684-5

Reference yield: 94.0%

5-dimethylaminonaphthalene-1-sulfonic acid N-(propyl)amide (54517-97-4) + (E)-1-(4-(bromomethyl)-phenyl)-2-phenyldiazene (145585-58-6) → N-(Azobenzene-4-ylmethyl)-5-dimethylaminonaphthalene-N-propyl-1-sulfonamide (426224-80-8)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 25 ℃; for 24h;

DOI:10.1039/b105497j

Reference yield: 56.0%

5-dimethylaminonaphthalene-1-sulfonic acid N-(propyl)amide (54517-97-4) + 3,5-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzylbromide (246140-08-9) → N-(3,5-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzyl)-N-propyl-(5'-dimethylaminonaphthalene-1'-sulfonic acid)amide

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 24h;

DOI:10.1002/chem.200601129

upstream raw materials:

propylamine

5-(dimethylamino)naphth-1-ylsulfonyl chloride

2-(N-tert-butoxycarbonylamino)ethanol

Downstream raw materials:

N-(Azobenzene-4-ylmethyl)-5-dimethylaminonaphthalene-N-propyl-1-sulfonamide

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