5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide

Base Information

• Chemical Name: 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide
• CAS No.: 62274-07-1
• Molecular Formula: C14H14N2O4S
• Molecular Weight: 306.342
• DSSTox Substance ID: DTXSID70604751
• Wikidata: Q82502773
• Mol file: 62274-07-1.mol

Synonyms:62274-07-1;5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide;SCHEMBL11370419;DTXSID70604751;AJAFTQHAPYNWRI-UHFFFAOYSA-N;3-methylamino-4-phenoxy-5-sulfamylbenzaldehyde

Chemical Property of 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 306.06742811
• Heavy Atom Count: 21
• Complexity: 442

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC1=C(C(=CC(=C1)C=O)S(=O)(=O)N)OC2=CC=CC=C2

Technology Process of 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide

There total 4 articles about 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide 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:

3-methylamino-4-phenoxy-5-sulfamylbenzyl alcohol (62273-28-3) + dichromic acid (13530-68-2) → 3-methylamino-4-phenoxy-5-sulfamylbenzaldehyde (62274-07-1)

Guidance literature:

With pyridine; In dichloromethane; acetone;

Reference yield:

3-methylamino-4-phenoxy-5-sulfamylbenzyl alcohol (62273-28-3) → 3-methylamino-4-phenoxy-5-sulfamylbenzaldehyde (62274-07-1)

Guidance literature:

With pyridine; chromium(VI) oxide; In dichloromethane; acetone;

Reference yield:

3-amino-4-phenoxy-5-sulfamylbenzyl alcohol (62273-23-8) → 3-methylamino-4-phenoxy-5-sulfamylbenzaldehyde (62274-07-1)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / N,N,N,N,N,N-hexamethylphosphoric triamide

2: pyridine; chromium(VI) oxide / dichloromethane; acetone

With pyridine; chromium(VI) oxide; sodium hydrogencarbonate; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; acetone;

upstream raw materials:

3-methylamino-4-phenoxy-5-sulfamylbenzyl alcohol

3-amino-4-phenoxy-5-sulfamylbenzyl alcohol

dichromic acid

Downstream raw materials:

5-Cyclopentylaminomethyl-3-methylamino-2-phenoxy-benzenesulfonamide