270148
Methyl (R)-(−)-3-hydroxy-2-methylpropionate
99%
Synonym(s):
(−)-Methyl D-β-hydroxyisobutyrate, (R)-(−)-3-Hydroxy-2-methylpropionic acid methyl ester
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Assay
99%
form
liquid
optical activity
[α]19/D −26°, c = 4 in methanol
optical purity
ee: 99% (GLC)
refractive index
n20/D 1.425 (lit.)
bp
76-77 °C/12 mmHg (lit.)
density
1.066 g/mL at 25 °C (lit.)
functional group
ester
hydroxyl
SMILES string
COC(=O)[C@H](C)CO
InChI
1S/C5H10O3/c1-4(3-6)5(7)8-2/h4,6H,3H2,1-2H3/t4-/m1/s1
InChI key
ATCCIZURPPEVIZ-SCSAIBSYSA-N
Related Categories
Application
Methyl (R)-(-)-3-hydroxy-2-methylpropionate may be used in the preparation of (S)-(4-benzyloxy-3-methylbut-1-ynyl)triethylsilane. It may also be used as a starting material in the total synthesis of (-)-discodermolide, (-)-stemoamide and (-)-stemospironine.
The (R)- and (S)-isomers are bifunctional building blocks for the synthesis of a wide variety of optically active molecules.
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
176.0 °F - closed cup
Flash Point(C)
80 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tetrahedron Letters, 34, 5939-5939 (1993)
Distinct binding and cellular properties of synthetic (+)-and (-)-discodermolides.
Chemistry & Biology, 1(1), 67-71 (1994)
Total Synthesis of (-)-Stemospironine.
Organic Letters, 3(17), 2721-2724 (2001)
Recent progress in the chemistry of the Stemona alkaloids.
Natural Product Reports, 17(1), 117-127 (2000)
Journal of the Chemical Society. Perkin Transactions 1, 759-759 (1993)
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