Catalog No.:AA00ED38

5636-65-7 | 5-Methylhex-4-enoic acid

Name: Name:5-Methylhex-4-enoic acid
Brand: AABLOCKS
SKU: AA00ED38
Availability: InStock
Rating: 90 (10 reviews)

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1mg

2 weeks

$247.00 $173.00

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2mg

2 weeks

$268.00 $188.00

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100mg

95%

2 weeks

$281.00 $197.00

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250mg

95%

2 weeks

$459.00 $322.00

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95%

2 weeks

$1,086.00 $760.00

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97%

2 weeks

$3,825.00 $2,678.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00ED38

Chemical Name:

5-Methylhex-4-enoic acid

CAS Number:

5636-65-7

Molecular Formula:

C7H12O2

Molecular Weight:

128.1690

MDL Number:

MFCD03425847

SMILES:

OC(=O)CCC=C(C)C

Properties

BP:

237.28°C (estimate)

Form:

Liquid

MP:

-28°C

Refractive Index:

1.4504

Storage:

Room Temperature;

Computed Properties

Complexity:

121

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.7

Downstream Synthesis Route

5636-65-7

2610-95-9

[1]Coulombel,Lydie;Dunach,Elisabet[SyntheticCommunications,2005,vol.35,#1,p.153-160]

[2]Linstead;Rydon[JournaloftheChemicalSociety,1933,p.583]

5636-65-7

65890-48-4

[1]Goetz,DanielB.;Holstein,SarahA.;Varney,MichelleL.;Wiemer,DavidF.[Bioorganicandmedicinalchemistry,2020,vol.28,#16]

[2]Staudinger;Ruzicka[HelveticaChimicaActa,1924,vol.7,p.385]

[3]Julia,S.;Linstrumelle,G.[BulletindelaSocieteChimiquedeFrance,1966,p.3490-3498]

[4]Meinwald,J.;Ouderkirk,J.T.[JournaloftheAmericanChemicalSociety,1960,vol.82,p.480-483]

[5]ArtmanIII,GeraldD.;Waldman,JacobH.;Weinreb,StevenM.[Synthesis,2002,#14,p.2057-2063]

[6]Bauer,Adriano;DiMauro,Giovanni;Li,Jing;Maulide,Nuno[AngewandteChemie-InternationalEdition,2020,vol.59,#41,p.18208-18212][Angew.Chem.,2020,vol.132,#41,p.18365-18369,5]

22539-81-7

5636-65-7

[1]Wills,VeronicaS.;Metzger,JosephI.;Allen,Cheryl;Varney,MichelleL.;Wiemer,DavidF.;Holstein,SarahA.[BioorganicandMedicinalChemistry,2017,vol.25,#8,p.2437-2444]

[2]Kim,Junsu;Lee,DaHye;Kim,Jinho[AdvancedSynthesisandCatalysis,2021,vol.363,#20,p.4728-4733]

[3]Davies,Jacob;Angelini,Lucrezia;Alkhalifah,MohammedA.;Sanz,LaiaMalet;Sheikh,NadeemS.;Leonori,Daniele[Synthesis,2018,vol.50,#4,p.821-830]

[4]Linstead;Rydon[JournaloftheChemicalSociety,1933,p.583]

[5]Cocker,Wesley;Geraghty,NiallW.A.;McMurry,T.BrianH.;Shannon,PatrickV.R.[JournaloftheChemicalSociety.PerkintransactionsI,1984,#10,p.2245-2254]

22539-80-6

5636-65-7

[1]Julia,S.;Linstrumelle,G.[BulletindelaSocieteChimiquedeFrance,1966,p.3490-3498]

[2]Akhnazaryan,A.A.etal.[JournalofgeneralchemistryoftheUSSR,1964,vol.34,p.1417-1422][ZhurnalObshcheiKhimii,1964,vol.34,#5,p.1413-1419]

[3]Cocker,Wesley;Geraghty,NiallW.A.;McMurry,T.BrianH.;Shannon,PatrickV.R.[JournaloftheChemicalSociety.PerkintransactionsI,1984,#10,p.2245-2254]

[4]Linstead;Rydon[JournaloftheChemicalSociety,1933,p.583]

[5]Davies,Jacob;Angelini,Lucrezia;Alkhalifah,MohammedA.;Sanz,LaiaMalet;Sheikh,NadeemS.;Leonori,Daniele[Synthesis,2018,vol.50,#4,p.821-830]

[6]Kim,Junsu;Lee,DaHye;Kim,Jinho[AdvancedSynthesisandCatalysis,2021,vol.363,#20,p.4728-4733]

23089-87-4

5636-65-7

[1]Mori,Kenji;Sugai,Takeshi;Maeda,Yukari;Okazaki,Tomomi;Noguchi,Tadashi;Naito,Hiroshi[Tetrahedron,1985,vol.41,#22,p.5307-5312]

[2]CurrentPatentAssignee:BRACCOSPA-US5688487,1997,A

[3]Conley,R.T.;Nowak,B.E.[JournalofOrganicChemistry,1962,vol.27,p.3196-3201]

Literature

Title: Photosonochemical catalytic ring opening of alpha-epoxyketones.

Journal: Beilstein journal of organic chemistry 20070101

Title: Chiral N-alkyl-2,4,6-triphenylpyridiniums as enantioselective triplet photosensitizers. laser flash photolysis and preparative studies.

Journal: The Journal of organic chemistry 20020726

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SDS