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446041 Aldrich

(1S,4R)-cis-4-Acetoxy-2-cyclopenten-1-ol

≥99%

Synonym: (1R,3S)-(+)-cis-4-Cyclopentene-1,3-diol 1-acetate, (1R,3S)-4-Cyclopentene-1,3-diol 1-acetate, (1R,4S)-cis-4-Hydroxy-2-cyclopentenyl acetate

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Properties

Related Categories Alcohols, Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Organic Building Blocks More...
InChI Key   IJDYOKVVRXZCFD-RQJHMYQMSA-N
assay   ≥99%
optical activity   [α]20/D +68°, c = 2.3 in chloroform
mp   49-51 °C(lit.)

Description

Application

Building block for the synthesis of carbocyclic nucleosides and prostaglandins.

Packaging

1 g in glass bottle

Bottomless glass bottle. Contents are inside inserted fused cone.

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Chiral Diols - Technical Article

Enantiomerically pure C2-symmetrical alkanediols such as (2S,5S)-, and (2R,5R)-hexanediol are valuable building blocks for the synthesis of chiral ligands such as (2S,5S)-dimethylpyrrolidine or (2S,5...
Aldrich ChemFiles 2005, 5.4, 12.
Keywords: Asymmetric synthesis, Building blocks, Catalysis, Chemfiles, Hydrogenations, Ligands

Peer-Reviewed Papers
15

References

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