(2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one

Base Information

• Chemical Name: (2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one
• CAS No.: 1353119-32-0
• Molecular Formula: C₁₅H₉FO₃
• Molecular Weight: 256.233
• DSSTox Substance ID: DTXSID701171269
• ChEMBL ID: CHEMBL1345096
• Mol file: 1353119-32-0.mol

Synonyms:(2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one;1353119-32-0;(Z)-2-(3-fluorobenzylidene)-6-hydroxybenzofuran-3(2H)-one;620545-88-2;MLS001215086;(2Z)-2-[(3-fluorophenyl)methylidene]-6-hydroxy-1-benzofuran-3-one;SMR000543181;cid_939330;CHEMBL1345096;BDBM76675;DTXSID701171269;HMS2861A09;MFCD04158995;STK923972;AKOS000270816;LS-05762;CS-0269131;EN300-36426;MLS-0327762.0002;(2Z)-2-(3-fluorobenzylidene)-6-hydroxy-coumaran-3-one;F2106-0006;Z119968780;(2Z)-2-[(3-Fluorophenyl)methylene]-6-hydroxy-3(2H)-benzofuranone;(2Z)-2-[(3-fluorophenyl)methylidene]-6-hydroxy-3-benzofuranone;(2Z)-2-[(3-fluorophenyl)methylidene]-6-oxidanyl-1-benzofuran-3-one;2-[(3-fluorophenyl)methylidene]-6-hydroxy-2,3-dihydro-1-benzofuran-3-one;(2Z)-2-[(3-fluorophenyl)methylidene]-6-hydroxy-2,3-dihydro-1-benzofuran-3-one

Chemical Property of (2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 256.05357231
• Heavy Atom Count: 19
• Complexity: 393

Purity/Quality:

99% ^*data from raw suppliers

(Z)-2-(3-Fluorobenzylidene)-6-hydroxybenzofuran-3(2H)-one 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)F)C=C2C(=O)C3=C(O2)C=C(C=C3)O
• Isomeric SMILES: C1=CC(=CC(=C1)F)/C=C\2/C(=O)C3=C(O2)C=C(C=C3)O

Technology Process of (2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one

There total 5 articles about (2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one 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: 74.4%

2-chloro-1-(2,4-dihydroxyphenyl)ethanone (25015-92-3) + 3-Fluorobenzaldehyde (456-48-4) → 6-hydroxy-3'-fluoroaurone (1353119-32-0,620545-88-2)

Guidance literature:

With potassium hydroxide; In ethanol; at 20 ℃;

Reference yield: 74.4%

2-chloro-1-(2,4-dihydroxyphenyl)ethanone (25015-92-3) + 3-Fluorobenzaldehyde (456-48-4) → (Z)-2-(3-fluorophenyl)methylene-5-hydroxy-3(2H)-benzofuranone (1353119-32-0,620545-88-2)

Guidance literature:

With potassium hydroxide; In methanol; water; at 20 ℃;

DOI:10.1002/jhet.2497

Reference yield: 68.7%

6-hydroxybenzofuran-3-one (6272-26-0) + 3-Fluorobenzaldehyde (456-48-4) → 6-hydroxy-3'-fluoroaurone (1353119-32-0,620545-88-2)

Guidance literature:

With potassium hydroxide; In water; at 25 ℃;

DOI:10.1002/bkcs.12215

upstream raw materials:

2-chloro-1-(2,4-dihydroxyphenyl)ethanone

3-Fluorobenzaldehyde

recorcinol

6-hydroxybenzofuran-3-one