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tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate

Base Information
  • Chemical Name:tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate
  • CAS No.:168134-60-9
  • Molecular Formula:C20H36O3Si2
  • Molecular Weight:380.675
  • Hs Code.:
tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate

Synonyms:tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate

Suppliers and Price of tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

Safty Information:
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Technology Process of tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate

There total 1 articles about tert-butyldimethylsilyl (2S)-(O-tert-butyldimethylsilyl)mandelate 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 1H-imidazole; In N,N-dimethyl-formamide; for 84h; Ambient temperature;
DOI:10.1016/0957-4166(95)00201-Y
Guidance literature:
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1016/0957-4166(95)00201-Y
Guidance literature:
Multi-step reaction with 2 steps
1: 237 mg / aq. NaOH / 1.75 h
2: 4 percent / diisopropylcarbodiimide; 4-(dimethylamino)pyridine / tetrahydrofuran / 2 h / 20 °C
With dmap; sodium hydroxide; diisopropyl-carbodiimide; In tetrahydrofuran; 1: Hydrolysis / 2: Esterification;
DOI:10.1021/jo981580+
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