446041
(1S,4R)-顺式-4-乙酰氧基-2-环戊烯-1-醇
≥99%
别名:
(1R,3S)-(+)-顺式-4-环戊烯-1,3-二醇1-乙酸酯, (1R,3S)-4-环戊烯-1,3-二醇-1-乙酸酯, (1R,4S)-顺式-4-羟基-2-环戊烯基乙酸酯
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关于此项目
经验公式（希尔记法）:
C7H10O3
化学文摘社编号:
分子量:
142.15
Beilstein:
4663992
MDL编号:
UNSPSC代码:
12352108
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
≥99%
表单
solid
旋光性
[α]20/D +68°, c = 2.3 in chloroform
mp
49-51 °C (lit.)
SMILES字符串
CC(=O)O[C@@H]1C[C@H](O)C=C1
InChI
1S/C7H10O3/c1-5(8)10-7-3-2-6(9)4-7/h2-3,6-7,9H,4H2,1H3/t6-,7+/m1/s1
InChI key
IJDYOKVVRXZCFD-RQJHMYQMSA-N
应用
(1S,4R)-cis-4-Acetoxy-2-cyclopenten-1-ol can be used as:
- A building block for the synthesis of biologically significant carbocyclic nucleosides and prostaglandins.
- A starting material in the synthesis of azasugar analogs.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Theil, F. et al.
Journal of the Chemical Society. Perkin Transactions 1, 255-255 (1996)
An improved preparation of highly enantiomerically enriched (R)-(+)-4-tert-butyldimethylsiloxy-2-cyclopenten-1-one
Myers AG, et al.
Tetrahedron Letters, 37(18), 3083-3086 (1996)
(4R)-(+)-tert-Butyldimethylsiloxy-2-Cyclopenten-1-one: 2-Cyclopenten-1-one, 4-[[(1, 1-dimethylethyl) dimethylsilyl] oxy]-,(R)-
Paquette LA,
Organic Syntheses, 73(18), 36-36 (1996)
Facile synthesis of 9-[(1′ R, 2′ S)-2′-hydroxy-3′-oxocyclopentan-1′-yl]-9-H-adenine possessing inhibitory activity against human recombinant S-adenosyl-l-homocysteine hydrolase
Kitade Y, et al.
Tetrahedron Letters, 42(3), 433-435 (2001)
Chemoenzymatic synthesis of carbocyclic nucleoside analogues with bicyclo [3.1. 0] hexyl residues
Theil F, et al.
Journal of the Chemical Society. Perkin Transactions 1, 255-258 (1996)
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