p-Cyclopentyloxybenzoyl chloride

Base Information

Chemical Name:p-Cyclopentyloxybenzoyl chloride
CAS No.:63763-05-3
Molecular Formula:C12H13ClO2
Molecular Weight:224.687
Hs Code.:
DSSTox Substance ID:DTXSID601297103

Synonyms:p-cyclopentyloxybenzoyl chloride;63763-05-3;4-cyclopentyloxybenzoyl chloride;SCHEMBL1027693;UNERQANHKKJITO-UHFFFAOYSA-N;4-(Cyclopentyloxy)benzoyl chloride;DTXSID601297103;AKOS000346309

Suppliers and Price of p-Cyclopentyloxybenzoyl chloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of p-Cyclopentyloxybenzoyl chloride

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:224.0604073
Heavy Atom Count:15
Complexity:216

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C1)OC2=CC=C(C=C2)C(=O)Cl

Technology Process of p-Cyclopentyloxybenzoyl chloride

There total 3 articles about p-Cyclopentyloxybenzoyl chloride 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:

: 30762-02-8
4-(cyclopentyloxy)benzoic acid

: 63763-05-3
p-cyclopentyloxybenzoyl chloride

Guidance literature:

Reference yield:

: 99-76-3,156291-94-0
methyl 4-hydroxylbenzoate

: 63763-05-3
p-cyclopentyloxybenzoyl chloride

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / Inert atmosphere

2: sodium hydroxide; water / ethanol / 1 h / 25 °C

3: N,N-dimethyl-formamide; oxalyl dichloride / 1 h / Inert atmosphere

With oxalyl dichloride; di-isopropyl azodicarboxylate; water; N,N-dimethyl-formamide; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.ejmech.2017.08.004

Reference yield:

: 63763-04-2
C₁₃H₁₆O₃

: 63763-05-3
p-cyclopentyloxybenzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide; water / ethanol / 1 h / 25 °C

2: N,N-dimethyl-formamide; oxalyl dichloride / 1 h / Inert atmosphere

With oxalyl dichloride; water; N,N-dimethyl-formamide; sodium hydroxide; In ethanol;
DOI:10.1016/j.ejmech.2017.08.004