Benzoic acid, 3-chloro-4-(2-propenyloxy)-

Base Information

• Chemical Name: Benzoic acid, 3-chloro-4-(2-propenyloxy)-
• CAS No.: 65650-44-4
• Molecular Formula: C10H9ClO3
• Molecular Weight: 212.633
• ChEMBL ID: CHEMBL1315741
• DSSTox Substance ID: DTXSID50472177
• Mol file: 65650-44-4.mol

Synonyms:3-Chloro-4-prop-2-enoxybenzoic acid;Benzoic acid, 3-chloro-4-(2-propenyloxy)-;65650-44-4;MLS001074422;SCHEMBL8460563;CHEMBL1315741;DTXSID50472177;HMS2211A17;HMS3335F20;AKOS000346206;SMR000673536;A1-05348

Chemical Property of Benzoic acid, 3-chloro-4-(2-propenyloxy)-

Chemical Property:

• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 212.0240218
• Heavy Atom Count: 14
• Complexity: 217

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCOC1=C(C=C(C=C1)C(=O)O)Cl

Technology Process of Benzoic acid, 3-chloro-4-(2-propenyloxy)-

There total 2 articles about Benzoic acid, 3-chloro-4-(2-propenyloxy)- 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: 81.2%

methyl 4-(allyloxy)-3-chlorobenzoate (65650-43-3) → 4-(allyloxy)-3-chlorobenzoic acid (65650-44-4)

Guidance literature:

With water; sodium hydroxide; In tetrahydrofuran; ethanol; at 20 ℃; for 1h;

Reference yield: 51.9%

aclofenac (22131-79-9) → 4-allyloxy-3-chloro-benzaldehyde (58236-91-2) + 4-(allyloxy)-3-chlorobenzoic acid (65650-44-4) + (4-allyloxy-3-chlorophenyl)methanol (144478-99-9)

Guidance literature:

With (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(III) chloride; iodosylbenzene; In dichloromethane; for 20h; Ambient temperature;

DOI:10.1016/S0040-4039(00)61242-X

upstream raw materials:

aclofenac

methyl 4-(allyloxy)-3-chlorobenzoate