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About This Item
經驗公式(希爾表示法):
C13H15NO3
CAS號碼:
分子量::
233.26
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
99%
形狀
solid
光學活性
[α]20/D −102°, c = 1 in ethanol
光學純度
ee: 99% (HPLC)
mp
44-46 °C (lit.)
官能基
phenyl
SMILES 字串
CCC(=O)N1[C@@H](COC1=O)Cc2ccccc2
InChI
1S/C13H15NO3/c1-2-12(15)14-11(9-17-13(14)16)8-10-6-4-3-5-7-10/h3-7,11H,2,8-9H2,1H3/t11-/m1/s1
InChI 密鑰
WHOBYFHKONUTMW-LLVKDONJSA-N
一般說明
應用
(R)-(−)-4-Benzyl-3-propionyl-2-oxazolidinone can be used as a building block for the preparation of methyl 3-[(S)-3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-methyl-3-oxopropyl]benzoate by treating with strong base followed by the addition of methyl 3-bromomethyl benzoate.[2]
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
Oxazolidinone cross-alkylation during Evans? asymmetric alkylation reaction
Fresno N, et al.
Tetrahedron, 67(47), 9104-9111 (2011)
A Synthetic Route to β-Hydroxytyrosine-Derived Tetramic Acids: Total Synthesis of the Fungal Metabolite F-14329
Bruckner, S, et al.
Chemistry?A European Journal , 23(24), 5692-5695 (2017)
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