5-Isopropyl-3-phenylisoxazole-4-carboxylic acid

Base Information

Chemical Name:5-Isopropyl-3-phenylisoxazole-4-carboxylic acid
CAS No.:92029-28-2
Molecular Formula:C₁₃H₁₃NO₃
Molecular Weight:231.251
Hs Code.:
European Community (EC) Number:816-932-3

Synonyms:5-isopropyl-3-phenylisoxazole-4-carboxylic acid;92029-28-2;3-phenyl-5-propan-2-yl-1,2-oxazole-4-carboxylic acid;3-phenyl-5-(propan-2-yl)-1,2-oxazole-4-carboxylic acid;AKOS013478934;CS-0258899;5-isopropyl-3-phenylisoxazole-4-carboxylicacid;EN300-717070;G48381;Z1201049952

Suppliers and Price of 5-Isopropyl-3-phenylisoxazole-4-carboxylic acid

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 4 raw suppliers

Chemical Property of 5-Isopropyl-3-phenylisoxazole-4-carboxylic acid

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:231.08954328
Heavy Atom Count:17
Complexity:274

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)C1=C(C(=NO1)C2=CC=CC=C2)C(=O)O

Technology Process of 5-Isopropyl-3-phenylisoxazole-4-carboxylic acid

There total 7 articles about 5-Isopropyl-3-phenylisoxazole-4-carboxylic 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:

: 1136-45-4
5-methyl-3-phenylisoxazol-4-carboxylic acid

: 92029-28-2
5-isopropyl-3-phenyl-isoxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, -78 deg C, 40 min

2: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, -78 deg C, 40 min

With n-butyllithium;
DOI:10.1021/jo00350a047

Reference yield:

: 16883-16-2
5-methyl-3-phenylisoxazole-4-carbonyl chloride

: 92029-28-2
5-isopropyl-3-phenyl-isoxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: CHCl₃ / 0 - 20 °C

2: thionyl chloride / CHCl₃ / 0 - 20 °C

3: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, from -78 deg C to RT, overnigh

4: 64 percent / 3 N aq. HCl / Heating

5: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, -78 deg C, 40 min

With hydrogenchloride; n-butyllithium; thionyl chloride; In chloroform;
DOI:10.1021/jo00350a047

Reference yield:

: 99298-89-2
5-Methyl-3-phenyl-isoxazole-4-carboxylic acid (2-hydroxy-1,1-dimethyl-ethyl)-amide

: 92029-28-2
5-isopropyl-3-phenyl-isoxazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / CHCl₃ / 0 - 20 °C

2: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, from -78 deg C to RT, overnigh

3: 64 percent / 3 N aq. HCl / Heating

4: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, -78 deg C, 40 min

With hydrogenchloride; n-butyllithium; thionyl chloride; In chloroform;
DOI:10.1021/jo00350a047