Falimint

Base Information

• Chemical Name: Falimint
• CAS No.: 553-20-8
• Molecular Formula: C11H14 N2 O4
• Molecular Weight: 238.243
• Hs Code.: 2924299090
• European Community (EC) Number: 611-256-3
• UNII: I26A23734J
• DSSTox Substance ID: DTXSID20203819
• Nikkaji Number: J10.628C
• Wikidata: Q4073296
• Metabolomics Workbench ID: 49223
• Mol file: 553-20-8.mol

Synonyms:1-propoxy-2-acetamino-2-nitrobenzol;1-propoxy-2-acetamino-4-nitrobenzene;5'-nitro-2'-propoxyacetanilide;acetylaminonitropropoxybenzene;Falimint

Chemical Property of Falimint

Chemical Property:

• Vapor Pressure: 6.2E-07mmHg at 25°C
• Melting Point: 102.5°C
• Refractive Index: 1.5700 (estimate)
• Boiling Point: 410°Cat760mmHg
• PKA: 13.61±0.70(Predicted)
• Flash Point: 201.8°C
• PSA: 87.64000
• Density: 1.244g/cm³
• LogP: 3.51470
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 238.09535693
• Heavy Atom Count: 17
• Complexity: 277

Purity/Quality:

98%Min ^*data from raw suppliers

N-(5-NITRO-2-PROPOXYPHENYL)ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCOC1=C(C=C(C=C1)[N+](=O)[O-])NC(=O)C

Technology Process of Falimint

There total 7 articles about Falimint 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-acetamido-4-nitrophenol (97-60-9) + propyl bromide (106-94-5) → 2-Acetamino-4-nitropropoxybenzen (553-20-8)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; for 8h; Heating;

Reference yield:

2-amino-4-nitro-1-propoxybenzene (553-79-7) + acetyl chloride (75-36-5) → 2-Acetamino-4-nitropropoxybenzen (553-20-8)

Guidance literature:

Reference yield:

acetic acid-(2-propoxy-anilide) (55792-51-3) → 2-Acetamino-4-nitropropoxybenzen (553-20-8)

Guidance literature:

With water; nitric acid;

upstream raw materials:

acetic acid-(2-propoxy-anilide)

2-amino-4-nitro-1-propoxybenzene

acetic anhydride

acetyl chloride

Downstream raw materials:

2-amino-4-nitro-1-propoxybenzene

Refernces