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4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, methyl ester

Base Information Edit
  • Chemical Name:4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, methyl ester
  • CAS No.:105623-34-5
  • Molecular Formula:C20H29NO5
  • Molecular Weight:363.454
  • Hs Code.:
  • Mol file:105623-34-5.mol
4-Isoxazolidinecarboxylic acid,
5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-,
methyl ester

Synonyms:

Suppliers and Price of 4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, methyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, methyl ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
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MSDS Files:
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Technology Process of 4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, methyl ester

There total 5 articles about 4-Isoxazolidinecarboxylic acid, 5-methyl-2-(phenylmethyl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-, 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:
Multi-step reaction with 4 steps
1: LAH
2: 18 percent / (COCl)2, DMSO, Et3N / CH2Cl2 / 15 h / -65 °C
3: 79 percent / diethyl ether / 1 h / 20 °C
4: 333 h / 20 °C
With lithium aluminium tetrahydride; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane;
Guidance literature:
Multi-step reaction with 3 steps
1: 18 percent / (COCl)2, DMSO, Et3N / CH2Cl2 / 15 h / -65 °C
2: 79 percent / diethyl ether / 1 h / 20 °C
3: 333 h / 20 °C
With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane;
Guidance literature:
Multi-step reaction with 3 steps
1: sodium cianoborohydride / methanol
2: 79 percent / diethyl ether / 1 h / 20 °C
3: 333 h / 20 °C
With sodium cyanoborohydride; In methanol; diethyl ether;
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