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Merck

459542

Sigma-Aldrich

(R)-(-)-4-苄基-3-丙酰基-2-噁唑烷酮

99%

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About This Item

经验公式(希尔记法):
C13H15NO3
分子量:
233.26
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

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

(R)-(−)-4-Benzyl-3-propionyl-2-oxazolidinone is used as a building block in organic synthesis for the preparation of oxazolidinone derivatives.

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.

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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