| Identification | Back Directory | [Name]
Dimethyl glutaconate | [CAS]
5164-76-1 | [Synonyms]
Nsc30046
Diemthyl glutaconate
DIMETHYL GLUTACONATE
DIMETHYL 2-PENTENOATE
DiMethyl pent-2-enedioate
Glutaconic acid dimethyl ester
Dimethyl Glutaconate (~25% cis)
DiMethyl Glutaconate (~10% Cis)
DiMethyl glutaconate >=97.0% (GC)
Dimethyl glutaconate, E/Z mixture
2-Pentenedioic acid, dimethyl ester
(E)-2-Pentenedioic acid dimethyl ester
2-Pentenedioic acid,1,5-dimethyl ester
(Z)-2-pentenedioic acid dimethyl ester | [Molecular Formula]
C7H10O4 | [MDL Number]
MFCD00066240 | [MOL File]
5164-76-1.mol | [Molecular Weight]
158.15 |
| Chemical Properties | Back Directory | [Boiling point ]
192.8±15.0 °C(Predicted) | [density ]
1.124 g/mL at 20 °C (lit.) | [refractive index ]
n20/D 1.452 | [Fp ]
>100 °C | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Oil | [color ]
Colourless | [BRN ]
1724169 | [InChI]
1S/C7H10O4/c1-10-6(8)4-3-5-7(9)11-2/h3-4H,5H2,1-2H3/b4-3+ | [InChIKey]
SKCGFFOFYXLNCG-ONEGZZNKSA-N | [SMILES]
COC(=O)C\C=C\C(=O)OC | [NIST Chemistry Reference]
2-Pentenedioic acid, dimethyl ester(5164-76-1) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36 | [Safety Statements ]
26 | [WGK Germany ]
3 | [REACH Registrations]
Active | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Aquatic Chronic 3 |
| Hazard Information | Back Directory | [Uses]
Dimethyl glutaconate may be used in the synthesis of:
- dimethyl 3-[(Z)-1-propenyl]glutarate
- phenanthridinone derivatives
- substituted benzenes
| [General Description]
Dimethyl glutaconate, also known as dimethyl 2-pentenoate, is a diester. It reacts with salicaldehyde in the presence of piperidine to form a coumarin-fused electron deficient diene. | [Synthesis]
Methanol (10.0 kg, 3.1 kmol), pent-2-enoic acid (5.57 kg, 0.043 kmol), and concentrated sulfuric acid (72.0 g) were sequentially added to a 20 L enameled reactor equipped with a mechanical stirrer and a thermometer. The reaction mixture was heated to reflux for the reaction. After completion of the reaction, methanol was recovered by distillation under reduced pressure. After the temperature was lowered to 20 °C, the reaction solution was washed with aqueous sodium carbonate to neutralize the acid and subsequently dried. Finally, the product was purified by vacuum distillation to give 6.22 kg of colorless liquid dimethyl pent-2-enoate in 91.5% yield and 81.6% total yield. The product was analyzed by gas chromatography (GC) with a purity of 98.8% (22.4% cis-isomer and 76.4% trans-isomer). | [References]
[1] Chemical Communications, 2015, vol. 51, # 77, p. 14505 - 14508
[2] Patent: CN108358783, 2018, A. Location in patent: Paragraph 0032; 0035
[3] Tetrahedron, 1992, vol. 48, # 46, p. 10103 - 10114 |
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J & K SCIENTIFIC LTD.
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Energy Chemical
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China Langchem Inc.
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Sigma-Aldrich
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