2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole

Base Information

• Chemical Name: 2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole
• CAS No.: 103089-75-4
• Molecular Formula: C14H10N2O3S
• Molecular Weight: 286.311
• DSSTox Substance ID: DTXSID00545461
• Wikidata: Q82422964
• Mol file: 103089-75-4.mol

Synonyms:103089-75-4;2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole;3-[(2-benzothiazolyl)methoxy]nitrobenzene;SCHEMBL10758257;DTXSID00545461;SWRYJOQVSHRUAJ-UHFFFAOYSA-N;AKOS008408646;3-[(2-benzthiazolyl)methoxy]nitrobenzene

Chemical Property of 2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 286.04121336
• Heavy Atom Count: 20
• Complexity: 350

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)N=C(S2)COC3=CC=CC(=C3)[N+](=O)[O-]

Technology Process of 2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole

There total 1 articles about 2-[(3-Nitrophenoxy)methyl]-1,3-benzothiazole 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:

2-amino-benzenethiol (137-07-5) → 3-[(2-benzothiazolyl)methoxy]nitrobenzene (103089-75-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 71 percent / CH₂Cl₂ / Ambient temperature

2: 84 percent / cesium carbonate, sodium carbonate, potassium iodide / acetone / Heating

With sodium carbonate; caesium carbonate; potassium iodide; In dichloromethane; acetone;

DOI:10.1021/jm00385a024

Reference yield: 90.0%

3-[(2-benzothiazolyl)methoxy]nitrobenzene (103089-75-4) → 3-[(2-benzothiazolyl)methoxy]aniline (103089-76-5)

Guidance literature:

With hydrogenchloride; iron; In ethanol; Ambient temperature;

DOI:10.1021/jm00385a024

Reference yield: 87.0%

3-[(2-benzothiazolyl)methoxy]nitrobenzene (103089-75-4) → <3-(2-benzthiazolylmethoxy)phenyl>hydroxyamine (104257-09-2)

Guidance literature:

With hydrazine hydrate; palladium on activated charcoal; In tetrahydrofuran; Ambient temperature;

DOI:10.1021/jm00385a024

upstream raw materials:

2-amino-benzenethiol

Downstream raw materials:

3-[(2-benzothiazolyl)methoxy]aniline

<3-(2-benzthiazolylmethoxy)phenyl>hydroxyamine

N-methyl-3-(2-benzthiazoylmethoxy)aniline

4-{[3-(2-benzthiazolylmethoxy)phenyl]amino}-4-oxo-butanoic acid