Dimethyl 3-hydroxyglutarate
Dimethyl 3-hydroxyglutarate Basic information
- Product Name:
- Dimethyl 3-hydroxyglutarate
- Synonyms:
-
- 3-hydroxyglutaric acid dimethyl ester
- Dimethyl 3-hydroxypentanedioate
- Pentanedioic acid, 3-hydroxy-, dimethyl ester
- NISTC7250557
- Glutaric acid, 3-hydroxy-, dimethyl ester
- Nsc30047
- Dimethyl 3-hydroxygl
- 3-Hydroxy-pentanedioic Acid DiMethyl Ester
- CAS:
- 7250-55-7
- MF:
- C7H12O5
- MW:
- 176.17
- Product Categories:
-
- C6 to C7
- Carbonyl Compounds
- Esters
- Building Blocks
- C6 to C7
- Carbonyl Compounds
- Chemical Synthesis
- Organic Building Blocks
- Aliphatics
- Mol File:
- 7250-55-7.mol
Dimethyl 3-hydroxyglutarate Chemical Properties
- Boiling point:
- 139-140 °C/8 mmHg (lit.)
- Density
- 1.192 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.442(lit.)
- Flash point:
- >230 °F
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform
- form
- Oil
- pka
- 12.60±0.20(Predicted)
- color
- Clear colourless to Pale Yellow
- BRN
- 1776666
- InChI
- InChI=1S/C7H12O5/c1-11-6(9)3-5(8)4-7(10)12-2/h5,8H,3-4H2,1-2H3
- InChIKey
- CUPGMRSSZADEIW-UHFFFAOYSA-N
- SMILES
- C(OC)(=O)CC(O)CC(OC)=O
- CAS DataBase Reference
- 7250-55-7(CAS DataBase Reference)
- NIST Chemistry Reference
- Glutaric acid, 3-hydroxy-, dimethyl ester(7250-55-7)
Safety Information
- Safety Statements
- 23-24/25
- WGK Germany
- 3
- HS Code
- 29181990
MSDS
- Language:English Provider:SigmaAldrich
Dimethyl 3-hydroxyglutarate Usage And Synthesis
Chemical Properties
Off-White to Pale Yellow Oil
Uses
Dimethyl 3-hydroxyglutarate was used in the synthesis of two chiral fragments representing C1-11 and C12-25 of the polyene macrolide pimaricin.
Uses
Glutaric Acid derivative
General Description
Enantioselective hydrolysis and ammonolysis of dimethyl-3-hydroxyglutarate has been studied using immobilized lipase B isolated from Candida antarctica.
Synthesis
1830-54-2
7250-55-7
To a stirred solution of dimethyl 3-oxoglutarate (17.7 mL, 120.6 mmol) in methanol (315 mL) at 0 °C was added sodium borohydride (3.9 g, 102.5 mmol) in batches. After the reaction mixture was brought to room temperature, the reaction was continued with stirring for 24 hours. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 5-6 by adding solid citric acid to quench the reaction. Subsequently, silica gel (about 1 g) was added to the reaction mixture and the solvent was removed by rotary evaporation. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:1) to afford dimethyl 3-hydroxyglutarate (19.98 g, 94% yield) as a colorless oil.
References
[1] Journal of the Brazilian Chemical Society, 2011, vol. 22, # 1, p. 172 - 175
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3650 - 3653
[3] Journal of Organic Chemistry, 1988, vol. 53, # 7, p. 1567 - 1569
[4] RSC Advances, 2016, vol. 6, # 27, p. 22737 - 22748
[5] Journal of the American Chemical Society, 2009, vol. 131, # 49, p. 17980 - 17985
Dimethyl 3-hydroxyglutarateSupplier
- Tel
- 025-58862853 18915922038
- sales@endesachem.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- 021-58099652-8005 13585536065
- bin.wu@shlschem.com
- Tel
- 025-83697070
- info@chemlin.com.cn
Dimethyl 3-hydroxyglutarate(7250-55-7)Related Product Information
- Dimethyl fumarate
- Dimethyl sebacate
- Dimethyl carbonate
- Diethyl 3-hydroxyglutarate
- Dimethyl sulfoxide
- N,N-Dimethylformamide
- Dimethyl ether
- 2-Ketoglutaric acid
- ETHANE
- Dimethyl phthalate
- Dimethyl Glutarate
- Glutaric acid
- MONOCROTALINE
- diethyl hydrogen 2-hydroxypropane-1,2,3-tricarboxylate
- TRIMETHYL CITRATE
- Tributyl citrate
- CITRIC ACID TRIALLYL ESTER
- AcidEster