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4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-

Base Information
  • Chemical Name:4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-
  • CAS No.:943130-42-5
  • Molecular Formula:C13H11NO3
  • Molecular Weight:229.235
  • Hs Code.:
  • Mol file:943130-42-5.mol
4-Isoxazolecarboxylic  acid,  5-cyclopropyl-3-phenyl-

Synonyms:4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-

Suppliers and Price of 4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-
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
  • American Custom Chemicals Corporation
  • 5-CYCLOPROPYL-3-PHENYLISOXAZOLE-4-CARBOXYLIC ACID 95.00%
  • 5MG
  • $ 505.90
Total 2 raw suppliers
Chemical Property of 4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-
Chemical Property:
  • PSA:63.33000 
  • LogP:2.91720 
Purity/Quality:

99% *data from raw suppliers

5-CYCLOPROPYL-3-PHENYLISOXAZOLE-4-CARBOXYLIC ACID 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl-

There total 4 articles about 4-Isoxazolecarboxylic acid, 5-cyclopropyl-3-phenyl- 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:
ethyl 5-cyclopropyl-3-phenyl-1,2-oxazole-4-carboxylate; With sodium hydroxide; water; In ethanol; at 80 ℃; for 3h;
With hydrogenchloride; In water; pH=1;
Guidance literature:
Multi-step reaction with 4 steps
1: sodium carbonate; hydroxylamine hydrochloride / water; ethanol / 2 h / 0 - 20 °C
2: N-chloro-succinimide / N,N-dimethyl-formamide / 0 - 20 °C
3: triethylamine / dichloromethane / 20 °C
4: lithium hydroxide monohydrate; water / ethanol / 50 °C
With N-chloro-succinimide; lithium hydroxide monohydrate; hydroxylamine hydrochloride; water; sodium carbonate; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 3 steps
1: N-chloro-succinimide / N,N-dimethyl-formamide / 0 - 20 °C
2: triethylamine / dichloromethane / 20 °C
3: lithium hydroxide monohydrate; water / ethanol / 50 °C
With N-chloro-succinimide; lithium hydroxide monohydrate; water; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;
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