(R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER
- Product Name
- (R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER
- CAS No.
- 72657-23-9
- Chemical Name
- (R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER
- Synonyms
- R-(-)-Roche Ester;(S)-Methyl 3-hydroxy-2-;(-)-Methyl 2-methylhydracrylate;METHYL D-(R)-3-HYDROXYISOBUTYRATE;(-)-methyl d-β-hydroxyisobutyrate;(R)-(-)-METHYL B-HYDROXYISOBUTYRATE;Methyle(R)-(-)-β-hydroxyisobutyrate;METHYL (R)-(-)-3-HYDROXYISOBUTYRATE;(-)-METHYL D-BETA-HYDROXYISOBUTYRATE;Methyl-D-(R)-beta-hydroxyisobutyrate
- CBNumber
- CB9226746
- Molecular Formula
- C5H10O3
- Formula Weight
- 118.13
- MOL File
- 72657-23-9.mol
(R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER Property
- Boiling point:
- 76-77 °C12 mm Hg(lit.)
- Density
- 1.066 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.425
- Flash point:
- 178 °F
- storage temp.
- Sealed in dry,2-8°C
- solubility
- Chloroform (Sparingly), Methanol (Slightly)
- pka
- 14.40±0.10(Predicted)
- form
- Liquid
- color
- Clear colorless
- optical activity
- [α]19/D −26°, c = 4 in methanol
- BRN
- 3587507
- InChI
- InChI=1S/C5H10O3/c1-4(3-6)5(7)8-2/h4,6H,3H2,1-2H3/t4-/m1/s1
- InChIKey
- ATCCIZURPPEVIZ-SCSAIBSYSA-N
- SMILES
- C(OC)(=O)[C@H](C)CO
- CAS DataBase Reference
- 72657-23-9(CAS DataBase Reference)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H227Combustible liquid
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P370+P378In case of fire: Use … for extinction.
P403+P235Store in a well-ventilated place. Keep cool.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- 270148
- Product name
- Methyl (R)-(?)-3-hydroxy-2-methylpropionate
- Purity
- 99%
- Packaging
- 1g
- Price
- $39.83
- Updated
- 2025/07/31
- Product number
- 270148
- Product name
- Methyl (R)-(?)-3-hydroxy-2-methylpropionate
- Purity
- 99%
- Packaging
- 5g
- Price
- $144.44
- Updated
- 2025/07/31
- Product number
- H0703
- Product name
- Methyl (R)-(-)-3-Hydroxyisobutyrate
- Purity
- >99.0%(GC)
- Packaging
- 5g
- Price
- $141
- Updated
- 2025/07/31
- Product number
- H0703
- Product name
- Methyl (R)-(-)-3-Hydroxyisobutyrate
- Purity
- >99.0%(GC)
- Packaging
- 25g
- Price
- $470
- Updated
- 2025/07/31
- Product number
- H943558
- Product name
- (R)-3-HydroxyisobutyricAcidMethylEster
- Packaging
- 2g
- Price
- $65
- Updated
- 2021/12/16
(R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER Chemical Properties,Usage,Production
Chemical Properties
Clear Colorless Oil
Uses
Chiral derivative of 3-Hydroxyisobutyrate.
Uses
The (R)- and (S)-isomers are bifunctional building blocks for the synthesis of a wide variety of optically active molecules.
Synthesis
15484-46-5
72657-23-9
GENERAL PROCEDURE: The general procedure for the synthesis of (-)-methyl-D-BETA-hydroxyisobutyrate from methyl 2-(hydroxymethyl)acrylate is as follows: the Ene-reductase activity assay needs to be carried out in anaerobic conditions (Coy Laboratory, Grass Lake, MI) at ambient temperature. Preparation of reaction stock solutions consisted of dissolving each substrate (see below for details) in 50 mM Tris-HCl buffer (pH 7.5) supplemented with 200 μM NADP+, 100 mM glucose, and glucose dehydrogenase (GDH) from Thermoplasma acidophilum (2 units were used for the IVTT reaction and 5 (2 units for the IVTT reaction and 5 units for the purified enzyme reaction). Individual substrate concentrations were selected to ensure that vmax conditions or maximum solubility were achieved. At these substrate concentrations, adjust reaction times to achieve 10-50% substrate conversion. For OYE activity assays in IVTT experiments, 20 μL of reaction stock solution was mixed with 2-10 μL of IVTT reaction mixture and the total assay volume was adjusted to 30 μL with 50 mM Tris-HCl (pH 7.5).For assays of purified OYE1 variants, the enzyme (final concentration: 250 nM) was added to 500 μL of reaction stock solution. The reaction process was quenched by removing a 30 μL aliquot from the assay solution and mixing it thoroughly with 30 μL of ethyl acetate containing 1 mM cyclohexanone (as internal standard). Organic phase samples were collected and analyzed by gas chromatography (GC) (see below for specific protocol). Enantiomeric/diastereoisomeric excesses were calculated by integrating the peak areas of the products and substrates. The relative conversion rate of each substrate was calculated by dividing the measured conversion rate of the OYE1 variant by the corresponding rate of wild-type OYE1.
References
[1] Advanced Synthesis and Catalysis, 2015, vol. 357, # 8, p. 1775 - 1786
[2] Tetrahedron Asymmetry, 2009, vol. 20, # 2, p. 210 - 213
[3] Angewandte Chemie - International Edition, 2009, vol. 48, # 12, p. 2162 - 2165
[4] Advanced Synthesis and Catalysis, 2008, vol. 350, # 16, p. 2533 - 2543
[5] Advanced Synthesis and Catalysis, 2010, vol. 352, # 14-15, p. 2663 - 2666
(R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from (R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER manufacturers
- Product
- (R)-(-)-3-HYDROXY-2-METHYLPROPIONIC ACID METHYL ESTER 72657-23-9
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1Ton
- Release date
- 2022-10-19
- Product
- (R)-(-)-3-Hydroxy-2-Methylpropionic Acid Methyl Ester 72657-23-9
- Price
- US $6.20/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 10KG
- Release date
- 2021-09-24
- Product
- (R)-Roche ester 72657-23-9
- Price
- US $6.20/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 10kg
- Release date
- 2021-09-24