5-Chloro-2-propoxybenzoic acid

Base Information

• Chemical Name: 5-Chloro-2-propoxybenzoic acid
• CAS No.: 62176-15-2
• Molecular Formula: C₁₀H₁₁ClO₃
• Molecular Weight: 214.649
• Hs Code.: 2918999090
• DSSTox Substance ID: DTXSID80402240
• Mol file: 62176-15-2.mol

Synonyms:5-chloro-2-propoxybenzoic acid;62176-15-2;5-chloro-2-propoxybenzoicacid;SCHEMBL20522075;DTXSID80402240;HMS1604I01;BBL014095;MFCD02729272;STK500997;AKOS005061905;VS-04177;CS-0191508;E89654;EN300-100720;Z111427908

Chemical Property of 5-Chloro-2-propoxybenzoic acid

Chemical Property:

• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 214.0396719
• Heavy Atom Count: 14
• Complexity: 196

Purity/Quality:

98%min ^*data from raw suppliers

5-chloro-2-propoxybenzoicAcid ^*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)Cl)C(=O)O

Technology Process of 5-Chloro-2-propoxybenzoic acid

There total 1 articles about 5-Chloro-2-propoxybenzoic acid 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:

→ 5-Chloro-2-propoxy-benzoic acid (62176-15-2)

Guidance literature:

Ethylester d. 5-Chlor-salicylsaeure, 1) Propylhalogenid, 2) Verseif.;

Reference yield: 90.4%

methanol (67-56-1) + 5-Chloro-2-propoxy-benzoic acid (62176-15-2) → methyl 5-chloro-2-propoxybenzoate (75230-38-5)

Guidance literature:

With sulfuric acid; for 6h; Heating;

Reference yield:

5-Chloro-2-propoxy-benzoic acid (62176-15-2) → N-(5-Chloro-2-propoxy-benzoyl)-N'-cyclooctyl-guanidine; hydrochloride (75230-21-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 90.4 percent / H₂SO₄ / 6 h / Heating

2: 52.2 percent / Na, HCl / methanol / 5 h / Ambient temperature

With hydrogenchloride; sulfuric acid; sodium; In methanol;

Downstream raw materials:

4-(2-<5-chloro-2-propoxy-benzamido>-ethyl)-2-methoxy-benzoic acid

methyl 5-chloro-2-propoxybenzoate

N-(5-Chloro-2-propoxy-benzoyl)-N'-cyclooctyl-guanidine; hydrochloride

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