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Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester

Base Information
  • Chemical Name:Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester
  • CAS No.:179165-13-0
  • Molecular Formula:C22H23NO4
  • Molecular Weight:365.429
  • Hs Code.:
  • Mol file:179165-13-0.mol
Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester

Synonyms:

Suppliers and Price of Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester
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
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester
Chemical Property:
Purity/Quality:

99.90% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester

There total 4 articles about Benzoic acid, 4-[3-[4-(pentyloxy)phenyl]-5-isoxazolyl]-, methyl ester 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:
Guidance literature:
With hydroxylamine hydrochloride; In 1-methyl-pyrrolidin-2-one; at 60 ℃; for 30h;
DOI:10.1021/op0497862
Guidance literature:
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 65 - 70 °C
2: potassium tert-butylate / N,N-dimethyl-formamide / 4 h / 20 - 25 °C / Large scale
3: hydroxylamine hydrochloride / 1-methyl-pyrrolidin-2-one / 30 h / 60 °C
With hydroxylamine hydrochloride; potassium tert-butylate; potassium carbonate; In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide; 2: |Aldol Condensation;
DOI:10.1021/op0497862
Guidance literature:
Multi-step reaction with 2 steps
1: potassium tert-butylate / N,N-dimethyl-formamide / 4 h / 20 - 25 °C / Large scale
2: hydroxylamine hydrochloride / 1-methyl-pyrrolidin-2-one / 30 h / 60 °C
With hydroxylamine hydrochloride; potassium tert-butylate; In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide; 1: |Aldol Condensation;
DOI:10.1021/op0497862
upstream raw materials:

1-Bromopentane

4-pentyloxyacetophenone

Downstream raw materials:

C21H21NO4

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