N'-(4-aminophenyl)sulfonylethanimidamide

Base Information

• Chemical Name: N'-(4-aminophenyl)sulfonylethanimidamide
• CAS No.: 5768-68-3
• Molecular Formula: C8H11 N3 O2 S
• Molecular Weight: 213.26
• NSC Number: 31858
• DSSTox Substance ID: DTXSID50973275
• Mol file: 5768-68-3.mol

Synonyms:N'-(4-aminophenyl)sulfonylethanimidamide;5768-68-3;DTXSID50973275;NSC31858;NSC-31858;N-(4-Aminobenzene-1-sulfonyl)ethanimidamide

Chemical Property of N'-(4-aminophenyl)sulfonylethanimidamide

Chemical Property:

• Boiling Point: 433.7°Cat760mmHg
• Flash Point: 216.1°C
• Density: 1.41g/cm³
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 213.05719778
• Heavy Atom Count: 14
• Complexity: 310

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=NS(=O)(=O)C1=CC=C(C=C1)N)N
• Isomeric SMILES: C/C(=N/S(=O)(=O)C1=CC=C(C=C1)N)/N

Technology Process of N'-(4-aminophenyl)sulfonylethanimidamide

There total 4 articles about N'-(4-aminophenyl)sulfonylethanimidamide 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:

→ sulphacetamide (5768-68-3)

Guidance literature:

With hydrogenchloride; iron;

DOI:10.1021/ja01264a014

Reference yield:

N-(N-acetyl-sulfanilyl)-acetamidine → sulphacetamide (5768-68-3)

Guidance literature:

With hydrogenchloride; ethanol;

DOI:10.1021/ja01243a016

Reference yield:

p-acetylaminobenzenesulfonyl chloride (121-60-8) → sulphacetamide (5768-68-3)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous acetone; aq. NaOH solution

2: hydrogen chloride; ethanol

With hydrogenchloride; sodium hydroxide; ethanol; acetone;

DOI:10.1021/ja01243a016

upstream raw materials:

sulfanilamide

O-ethyl acetimidate

p-acetylaminobenzenesulfonyl chloride

Downstream raw materials:

sulphaacetamide