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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选择尺寸
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
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4663992
Assay:
≥99%
Form:
solid
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
SMILES string
CC(=O)O[C@@H]1C[C@H](O)C=C1
InChI key
IJDYOKVVRXZCFD-RQJHMYQMSA-N
assay
≥99%
form
solid
optical activity
[α]20/D +68°, c = 2.3 in chloroform
mp
49-51 °C (lit.)
Quality Level
Application
(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.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Synthesis of base-modified noraristeromycin derivatives and their inhibitory activity against human and Plasmodium falciparum recombinant S-adenosyl-L-homocysteine hydrolase
Kitade Y, et al.
Tetrahedron, 58(7), 1271-1277 (2002)
Myers, A.G. et al.
Tetrahedron Letters, 37, 3083-3083 (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)
Theil, F. et al.
Journal of the Chemical Society. Perkin Transactions 1, 255-255 (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)
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