3-Fluoro-N-hydroxy-benzamidine

Base Information

• Chemical Name: 3-Fluoro-N-hydroxy-benzamidine
• CAS No.: 54872-79-6
• Molecular Formula: C7H7FN2O
• Molecular Weight: 154.144
• Hs Code.: 2925290090
• DSSTox Substance ID: DTXSID00399204
• Mol file: 54872-79-6.mol

Synonyms:3-Fluoro-N-hydroxy-benzamidine;3-fluoro-N'-hydroxybenzenecarboximidamide;54872-79-6;3-fluoro-N'-hydroxybenzimidamide;N-Hydroxy-3-fluoro-benzamidine;DTXSID00399204;WPJZGPLKRBIDGD-UHFFFAOYSA-N;3-FLUORO-N'-HYDROXYBENZAMIDINE;AKOS016906256;3-fluoro-N-hydroxybenzenecarboximidamide;s11392;3-fluoro-N-hydroxybenzene-carboximidamide

Chemical Property of 3-Fluoro-N-hydroxy-benzamidine

Chemical Property:

• PSA: 58.61000
• LogP: 1.62050
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 154.05424101
• Heavy Atom Count: 11
• Complexity: 161

Purity/Quality:

97% ^*data from raw suppliers

3-Fluoro-N-hydroxy-benzamidine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)F)C(=NO)N

Technology Process of 3-Fluoro-N-hydroxy-benzamidine

There total 7 articles about 3-Fluoro-N-hydroxy-benzamidine 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: 100.0%

m-Fluorobenzonitrile (403-54-3) → 3-fluoro-N'-hydroxybenzenecarboximidamide (54872-79-6,1319746-46-7)

Guidance literature:

With hydroxylamine monohydrate; In ethanol; at 90 ℃; for 1h; Sealed tube;

DOI:10.1016/j.ejmech.2018.10.015

Reference yield: 99.0%

→ 3-fluoro-N'-hydroxybenzenecarboximidamide (54872-79-6,1319746-46-7)

Guidance literature:

Reference yield: 96.0%

m-Fluorobenzonitrile (403-54-3) → 3-fluoro-N-hydroxybenzene-1-carboximidamide (54872-79-6)

Guidance literature:

m-Fluorobenzonitrile; With hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine; In ethanol; at 70 ℃; for 48h;

With sodium hydroxide; In dichloromethane; water; pH=9 - 10;

upstream raw materials:

3-fluorobenzene-1-carbothioamide

m-Fluorobenzonitrile

3-fluorobromobenzene

3-Cyanobenzaldehyde

Downstream raw materials:

5-ferrocenyl-3-(3-fluorophenyl)-1,2,4-oxadiazole

3-(3-fluoro-phenyl)-5-(2-nitro-3-methylphenyl)-1,2,4-oxadiazole

3-(3-fluorophenyl)-5-(3-indazolyl)-1,2,4-oxadiazole