Catalog No.:AA002ZZ5

30414-53-0 | Methyl 3-oxovalerate

Name: Name:Methyl 3-oxovalerate
Brand: AABLOCKS
SKU: AA002ZZ5
Availability: InStock
Rating: 90 (10 reviews)

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98%

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25g

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$16.00 $11.00

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100g

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500g

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA002ZZ5

Chemical Name:

Methyl 3-oxovalerate

CAS Number:

30414-53-0

Molecular Formula:

C6H10O3

Molecular Weight:

130.1418

MDL Number:

MFCD00011705

SMILES:

CCC(=O)CC(=O)OC

Properties

BP:

207.8°C at 760 mmHg

Form:

Liquid

MP:

-35 °C

Refractive Index:

n20/D 1.422(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

118

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

0.4

Upstream Synthesis Route

30414-53-0

3473-63-0

124703-78-2

[1]JournalofHeterocyclicChemistry,1992,vol.29,#5,p.1369-1370

[2]Patent:US5278175,1994,A,

30414-53-0

5734-67-8

[1]JournalofMedicinalChemistry,2014,vol.57,#6,p.2429-2439

30414-53-0

95-54-5

52099-72-6

[1]Patent:US5652246,1997,A,

30414-53-0

50405-45-3

[1]Heterocycles,2000,vol.53,#3,p.549-552

41340-36-7

30414-53-0

41340-25-4

[1]CroaticaChemicaActa,2016,vol.89,#4,

Downstream Synthesis Route

455-14-1

30414-53-0

749921-32-2

[1]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page74-75

[2]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page82-83

[3]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page83

[4]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page82

[5]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page81-82

[6]Bradbury;Allott;Dennis;Fisher;Major;Masek;Oldham;Pearce;Rankine;Revill;Roberts;Russell[JournalofMedicinalChemistry,1992,vol.35,#22,p.4027-4038]

30414-53-0

60789-54-0

129512-09-0

[1]Synthesis,1990,p.382-386

30414-53-0

3473-63-0

124703-78-2

[1]JournalofHeterocyclicChemistry,1992,vol.29,p.1369-1370

[2]Patent:US5278175,1994,A

30414-53-0

methyl(3R)-3-hydroxypentanoate

42558-50-9

[1]TetrahedronLetters,1986,vol.27,p.2657-2660

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[3]ChemistryLetters,1987,p.679-682

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[27]AdvancedSynthesisandCatalysis,2013,vol.355,p.209-219

[28]AdvancedSynthesisandCatalysis,2013,vol.355,p.209-219

[29]EuropeanJournalofInorganicChemistry,2017,vol.2017,p.2762-2773

30414-53-0

42558-50-9

[1]TetrahedronAsymmetry,1991,vol.2,p.569-592

[2]TetrahedronAsymmetry,1994,vol.5,p.675-690

[3]JournalofOrganicChemistry,2004,vol.69,p.7577-7581

[4]ChemicalCommunications,2019,vol.56,p.157-160

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[8]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5856-5858

[9]TetrahedronLetters,1995,vol.36,p.4801-4804

[10]JournaloftheAmericanChemicalSociety,1995,vol.117,p.4423-4424

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Literature

Title: 2-Ethyl 4-methyl 5-ethyl-3-methyl-1H-pyrrole-2,4-dicarboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20120201

Title: Dimethyl 3,5-diethyl-1H-pyrrole-2,4-dicarboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20110801

Title: Studies on the synthesis and biological activitiy of 6-ethyl-4-aryl-5-methoxycarbonyl-3,4-dihydropyrimidin-2(1H)-ones.

Journal: Arzneimittel-Forschung 20070101

Title: Synthesis of 4-aryl-3,4-dihydropyrimidin-2(1H)-thione derivatives as potential calcium channel blockers.

Journal: Bioorganic & medicinal chemistry 20061215

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