00848
(1R,4S)-顺式-4-乙酰氧基-2-环戊烯-1-醇
≥98.0% (sum of enantiomers, GC)
别名:
(1S,4R)-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
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4350633
eCl@ss:
32035490
Quality Segment
assay
≥98.0% (sum of enantiomers, GC)
optical activity
[α]20/D −67±2°, c = 2.3% in chloroform
reaction suitability
reagent type: chrial catalyst
mp
49-51 °C
functional group
ester, hydroxyl
SMILES string
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+/m0/s1
InChI key
IJDYOKVVRXZCFD-NKWVEPMBSA-N
Application
(1R,4S)-cis-4-Acetoxy-2-cyclopenten-1-ol can be used as a reactant in the total synthesis of Bartlett′s brefeldin intermediate, spinosyn A analogs, (+)-7-deaza-5′-noraristeromycin, (±) strychnine and the Wieland-Gumlich aldehyde.
存储类别
11 - Combustible Solids
WGK
WGK 3
PPE（个人防护设备）
Eyeshields, Gloves, type N95 (US)
闪点 (F)
No data available
闪点 (°C)
No data available