1-AMINO-6-(2-NITROBENZENESULFONAMIDO)HEXANE HYDROCHLORIDE

Base Information

• Chemical Name: 1-AMINO-6-(2-NITROBENZENESULFONAMIDO)HEXANE HYDROCHLORIDE
• CAS No.: 95915-82-5
• Molecular Formula: C₁₂H₁₉N₃O₄S*ClH
• Molecular Weight: 337.827
• Mol file: 95915-82-5.mol

Synonyms:Benzenesulfonamide,N-(6-aminohexyl)-2-nitro-, monohydrochloride (9CI); Benzenesulfonamide,N-(6-aminohexyl)-o-nitro-, hydrochloride (7CI)

Chemical Property of 1-AMINO-6-(2-NITROBENZENESULFONAMIDO)HEXANE HYDROCHLORIDE

Chemical Property:

• Vapor Pressure: 1.87E-10mmHg at 25°C
• Melting Point: 162.0 to 167.0 °C
• Boiling Point: 502°C at 760 mmHg
• Flash Point: 257.4°C
• PSA: 126.39000
• LogP: 4.88940
• Solubility.: soluble in Methanol

Purity/Quality:

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

N-(6-Aminohexyl)-2-nitrobenzenesulfonamide Hydrochloride >95.0%(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-AMINO-6-(2-NITROBENZENESULFONAMIDO)HEXANE HYDROCHLORIDE

There total 3 articles about 1-AMINO-6-(2-NITROBENZENESULFONAMIDO)HEXANE HYDROCHLORIDE 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:

[6-(2-Nitrobenzenesulfonylamino)-hexyl]-carbamic acid t-butyl ester (191932-18-0) → N-(6-amino-hexyl)-2-nitro-benzenesulfonamide; hydrochloride (95915-82-5)

Guidance literature:

With hydrogenchloride; In methanol; for 1h;

DOI:10.1021/jo0507486

Reference yield:

1,6-Hexanediamine (124-09-4) → N-(6-amino-hexyl)-2-nitro-benzenesulfonamide; hydrochloride (95915-82-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 79 percent / CH₂Cl₂ / 20 °C

2: 57 percent / triethylamine / CH₂Cl₂ / 20 °C

3: 3.90 g / HCl / methanol / 1 h

With hydrogenchloride; triethylamine; In methanol; dichloromethane;

DOI:10.1021/jo0507486

Reference yield:

tert-butyl N-(6-aminohexyl)carbamate (51857-17-1) → N-(6-amino-hexyl)-2-nitro-benzenesulfonamide; hydrochloride (95915-82-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 57 percent / triethylamine / CH₂Cl₂ / 20 °C

2: 3.90 g / HCl / methanol / 1 h

With hydrogenchloride; triethylamine; In methanol; dichloromethane;

DOI:10.1021/jo0507486

upstream raw materials:

[6-(2-Nitrobenzenesulfonylamino)-hexyl]-carbamic acid t-butyl ester

1,6-Hexanediamine

tert-butyl N-(6-aminohexyl)carbamate

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