所有图片(1)
经验公式（希尔记法）:
C10H22O2Si2
CAS号:
分子量:
230.45
Beilstein:
1367530
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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检测方案
≥95%
折射率
n20/D 1.435 (lit.)
bp
58-59 °C/2 mmHg (lit.)
密度
0.897 g/mL at 25 °C (lit.)
SMILES字符串
C[Si](C)(C)OC1=C(CC1)O[Si](C)(C)C
InChI
1S/C10H22O2Si2/c1-13(2,3)11-9-7-8-10(9)12-14(4,5)6/h7-8H2,1-6H3
InChI key
WOBRFSDEZREQAB-UHFFFAOYSA-N
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一般描述
Photocycloaddition of 2-cyclohexenones to 1,2-bis(trimethyl-siloxy)cyclobutene has been studied. It undergoes Aldol condensation reaction with carbonyl compounds. It reacts with Br2 to give cyclobutanedione.
应用
1,2-Bis(trimethylsiloxy)cyclobutene has been used in the synthesis of:
- functionalized decalins, required for the total synthesis of various sesquiterpenes and diterpenes
- angularly substituted bicyclo[4.3.0]nona-2,5-diones and bicyclo-[4.4.0]deca-2,5-diones
- 3-methoxyestra-1,3,5,8,14-pentaen-17-one
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Photoaddition with 1, 2-bis (trimethylsiloxy) cyclobutene: a versatile entry to the stereocontrolled total synthesis of various sesquiterpenes and diterpenes.
de Keukeleire D, et al.
Journal of Photochemistry, 28(2), 165-174 (1985)
Organic Syntheses, 7, 112-112 (1990)
A (Π2+ Π2) photocycloaddition reaction as a facile route to angularly substituted cis-hydrindanes and cis-decalanes.
Van Audenhove M, et al.
Tetrahedron Letters, 21(20), 1979-1982 (1980)
Journal of the American Chemical Society, 106, 1759-1759 (1984)
A very short synthesis of 3-methoxyestra-1, 3, 5, 8, 14-pentaen-17-one.
Burnell DJ and Wu Y-J.
Canadian Journal of Chemistry, 67(5), 816-819 (1985)
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