(R)-(+)-α-Hydroxy-γ-butyrolactone - 98%, high purity , CAS No.56881-90-4

  • ≥98%
Item Number
R160929
Grouped product items
SKUSizeAvailabilityPrice Qty
R160929-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$148.90
R160929-250mg
250mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$333.90

Discover (R)-(+)-α-Hydroxy-γ-butyrolactone by Aladdin Scientific in 98% for only $148.90. Available - in Ligands at Aladdin Scientific. Tags: asymmetric synthesis, Chiral heterocyclic block.

Basic Description

Synonyms(R)-dihydro-3-hydroxyfuran-2(3H)-one | AS-61367 | (3R)-3-hydroxyoxolan-2-one | AKOS015909640 | SCHEMBL183974 | SG03T0K3QH | 2-HYDROXY-.GAMMA.-BUTYROLACTONE, (+)- | IDI1_015695 | T72635 | UNII-SG03T0K3QH | EN300-2009870 | Q27289197 | 2-HYDROXY-.GAMMA.-BUTY
Specifications & Purity≥98%
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
Product Description

Application:

(R)-(+)-α-Hydroxy-γ-butyrolactone can be used as a starting material to synthesize:

δ-Azaproline by reacting with benzyloxycarbonyl aminophthalimide via Mitsunobu reactions;

Homochiral (R)-2,4-dihydroxybutyramide seco-pseudonucleoside reagents;

Botryolide B via esterification and ring-closing metathesis reaction;

Pregnane derivatives containing γ-butyrolactones as potential glucocorticoid agonists;

Names and Identifiers

IUPAC Name (3R)-3-hydroxyoxolan-2-one
INCHI InChI=1S/C4H6O3/c5-3-1-2-7-4(3)6/h3,5H,1-2H2/t3-/m1/s1
InChi Key FWIBCWKHNZBDLS-GSVOUGTGSA-N
Canonical SMILES C1COC(=O)C1O
Isomeric SMILES C1COC(=O)[C@@H]1O
WGK Germany 3
PubChem CID 7157070
Molecular Weight 102.09
Beilstein 80588
Reaxy-Rn 80588

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SensitivityMoisture Sensitive
Refractive Index1.47
Specific Rotation[α]71.5° (C=1,CHCl3)
Flash Point(°F)>235.4 °F
Flash Point(°C)>113 °C
Boil Point(°C)133°C/10mmHg(lit.)

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 80588

Related Documents

References

1. Natalia N Dioubankova,Andrey D Malakhov,Dmitry A Stetsenko,Vladimir A Korshun,Michael J Gait.  (2002-12-20)  (R)-2,4-Dihydroxybutyramide seco-pseudonucleosides: new versatile homochiral synthons for synthesis of modified oligonucleotides..  Organic letters,  ((26)): (4607-4610).  [PMID:12489941]
2. Xiaohui Gou,Yifan Xue,Huiwen Zheng,Guobin Yang,Shuo Chen,Zhi Chen,Guohua Yuan.  (2020-07-17)  Gelatinases Cleave Dentin Sialoprotein Intracellularly..  Frontiers in physiology,  11  (686-686).  [PMID:32670089]

Solution Calculators