所有图片(1)
About This Item
经验公式（希尔记法）:
C4H8O3
CAS号:
分子量:
104.10
Beilstein:
103177
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案
99%
表单
liquid
折射率
n20/D 1.409 (lit.)
沸点
129-130 °C (lit.)
密度
1.092 g/mL at 25 °C (lit.)
官能团
ether
SMILES字符串
COC1OCCO1
InChI
1S/C4H8O3/c1-5-4-6-2-3-7-4/h4H,2-3H2,1H3
InChI key
VRAYTNFBRROPJU-UHFFFAOYSA-N
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应用
2-Methoxy-1,3-dioxolane was used in the synthesis of :
- [4,5-bis(hydroxymethyl)-1,3-dioxolan-2-yl]nucleosides, potential inhibitors of HIV
- diastereoisomeric cyclic acetals
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Synthesis of highly substituted 2, 6-anti-configured tetrahydropyrans. First steps towards an efficient access to amphidinol 3 ring system.
Dubost C, et al.
Tetrahedron Letters, 46(23), 4005-4009 (2005)
Jonas Brånalt et al.
The Journal of organic chemistry, 61(11), 3599-3603 (1996-05-31)
The synthesis of 1,3-dioxolan-2-ylnucleosides and related chemistry is described. We have shown that 2-methoxy-1,3-dioxolane (6) reacts with silylated thymine and trimethylsilyl triflate to give the acyclic formate ester 1-[2-(formyloxy)ethyl]thymine (8) rather than 1-(1,3-dioxolan-2-yl)thymine (7). A tentative mechanism which could explain
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