23434-88-0,MFCD17167032
Catalog No.:AA002N4Y

23434-88-0 | 1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$38.00   $27.00
- +
250mg
97%
in stock  
$57.00   $40.00
- +
1g
97%
in stock  
$137.00   $96.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002N4Y
Chemical Name:
1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-
CAS Number:
23434-88-0
Molecular Formula:
C17H23NO3
Molecular Weight:
289.3694
MDL Number:
MFCD17167032
SMILES:
O=C(N1CCCCC1)CCCCc1ccc2c(c1)OCO2
Properties
Computed Properties
 
Complexity:
341  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Pfeiffer;Loewe[JournalfurpraktischeChemie(Leipzig1954),1937,vol.<2>147,p.293,303]

[2]Koul,Surrinder;Koul,JawahirL.;Taneja,SubhashC.;Dhar,KanayaL.;Jamwal,DeshvirS.;Singh,Kuldeep;Reen,RashmeetK.;Singh,Jaswant[BioorganicandMedicinalChemistry,2000,vol.8,#1,p.251-268]

[1]Olofson,R.A.;Abbott,DuainE.[JournalofOrganicChemistry,1984,vol.49,#15,p.2795-2799]

[2]Ablordeppey,SethY.;Fischer,JamesB.;Glennon,RichardA.[BioorganicandMedicinalChemistry,2000,vol.8,#8,p.2105-2111]

[1]Sondengam,B.Lucas;Fomum,Z.Tanee;Charles,Georges;Akam,T.Mac[JournaloftheChemicalSociety.PerkintransactionsI,1983,p.1219-1222]

[2]Locationinpatent:experimentalpartSangwan,PayareL.;Koul,JawahirL.;Koul,Surrinder;Reddy,MallepallyV.;Thota,Niranjan;Khan,InshadA.;Kumar,Ashwani;Kalia,NitinP.;Qazi,GhulamN.[BioorganicandMedicinalChemistry,2008,vol.16,#22,p.9847-9857]

[3]Locationinpatent:experimentalpartCorrea,EdwinAndrés;Högestätt,EdwardD.;Sterner,Olov;Echeverri,Fernando;Zygmunt,PeterM.[BioorganicandMedicinalChemistry,2010,vol.18,#9,p.3299-3306]

[4]Locationinpatent:experimentalpartPedersen,MikaelE.;Metzler,Bjorn;Stafford,GaryI.;VanStaden,Johannes;Jaeger,AnnaK.;Rasmussen,HasseB.[Molecules,2009,vol.14,#9,p.3833-3843]

[5]Ribeiro,TatianaSantana;Freire-De-Lima,Leonardo;Previato,JoseOsvaldo;Mendonca-Previato,Lucia;Heise,Norton;DeLima,MarcoEdilsonFreire[BioorganicandMedicinalChemistryLetters,2004,vol.14,#13,p.3555-3558]

[6]Venkatasamy,Radhakrishnan;Faas,Laura;Young,AntonyR.;Raman,Amala;Hider,RobertC.[BioorganicandMedicinalChemistry,2004,vol.12,#8,p.1905-1920]

[7]Nakamura,Norio;Kiuchi,Fumiyuki;Tsuda,Yoshisuke[Chemicalandpharmaceuticalbulletin,1988,vol.36,#7,p.2647-2651]

[8]Jain,A.K.;Sharma,N.D.;Gupta,S.R.[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1986,vol.25,p.979]

[9]Ablordeppey,SethY.;Fischer,JamesB.;Glennon,RichardA.[BioorganicandMedicinalChemistry,2000,vol.8,#8,p.2105-2111]

[10]Locationinpatent:schemeortableMu,Li-Hua;Wang,Bo;Ren,Hao-Yang;Liu,Ping;Guo,Dai-Hong;Wang,Fu-Meng;Bai,Lin;Guo,Yan-Shen[BioorganicandMedicinalChemistryLetters,2012,vol.22,#9,p.3343-3348]

[11]Fokoue;Marques;Correia;Yamaguchi;Qu;Aires-De-Sousa;Scotti;Lopes;Kato[RSCAdvances,2018,vol.8,#38,p.21407-21413]

[12]CurrentPatentAssignee:CIPLALTD-WO2019/73491,2019,A1Locationinpatent:Page/Pagecolumn9;15

110-89-4   
C15H18O6 
  23434-88-0 

[1]Kiuchi,Fumiyuki;Nakamura,Norio;Saito,Makiko;Komagome,Kazue;Hiramatsu,Hirokuni;Takimoto,Noriaki;Akao,Nobuaki;Kondo,Kaoru;Tsuda,Yoshisuke[ChemicalandPharmaceuticalBulletin,1997,vol.45,#4,p.685-696]

94-62-2    23434-88-0   
(E)-5-(benzod1,3dioxol-5-yl)-1-(piperidin-1-yl)pent-4-en-1-one 

[1]Das,Biswanath;Kashinatham;Madhusudhan[TetrahedronLetters,1998,vol.39,#7,p.677-678]

Literature

Title: Synthesis and inhibitory effect of piperine derivates on monoamine oxidase.

Journal: Bioorganic & medicinal chemistry letters 20120501

Title: In vitro TRPV1 activity of piperine derived amides.

Journal: Bioorganic & medicinal chemistry 20100501

Title: Piperine analogs as potent Staphylococcus aureus NorA efflux pump inhibitors.

Journal: Bioorganic & medicinal chemistry 20081115

Title: Madhusudhan P, et al. Tetrahydropiperine, the first natural aryl pentanamide from Piper longum. Biochem Syst Ecol. 2001 May;29(5):537-538.

Title: Koul S, et al. Structure-activity relationship of piperine and its synthetic analogues for their inhibitory potentials of rat hepatic microsomal constitutive and inducible cytochromeP450 activities. Bioorg Med Chem. 2000 Jan;8(1):251-68.

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SDS
Related Products of 23434-88-0
Tags:23434-88-0 Molecular Formula|23434-88-0 MDL|23434-88-0 SMILES|23434-88-0 1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-
Catalog No.: AA002N4Y
23434-88-0,MFCD17167032
23434-88-0 | 1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-
Pack Size: 100mg
Purity: 97%
in stock
$38.00 $27.00
Pack Size: 250mg
Purity: 97%
in stock
$57.00 $40.00
Pack Size: 1g
Purity: 97%
in stock
$137.00 $96.00
Quantity
- +
Add to Card
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Technical Information
Catalog Number: AA002N4Y
Chemical Name: 1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-
CAS Number: 23434-88-0
Molecular Formula: C17H23NO3
Molecular Weight: 289.3694
MDL Number: MFCD17167032
SMILES: O=C(N1CCCCC1)CCCCc1ccc2c(c1)OCO2
Properties
Complexity: 341  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.2  
Downstream Synthesis Route
110-89-4    1029101-17-4    23434-88-0 

[1]Pfeiffer;Loewe[JournalfurpraktischeChemie(Leipzig1954),1937,vol.<2>147,p.293,303]

[2]Koul,Surrinder;Koul,JawahirL.;Taneja,SubhashC.;Dhar,KanayaL.;Jamwal,DeshvirS.;Singh,Kuldeep;Reen,RashmeetK.;Singh,Jaswant[BioorganicandMedicinalChemistry,2000,vol.8,#1,p.251-268]

23434-88-0    90670-01-2 

[1]Olofson,R.A.;Abbott,DuainE.[JournalofOrganicChemistry,1984,vol.49,#15,p.2795-2799]

[2]Ablordeppey,SethY.;Fischer,JamesB.;Glennon,RichardA.[BioorganicandMedicinalChemistry,2000,vol.8,#8,p.2105-2111]

94-62-2    23434-88-0 

[1]Sondengam,B.Lucas;Fomum,Z.Tanee;Charles,Georges;Akam,T.Mac[JournaloftheChemicalSociety.PerkintransactionsI,1983,p.1219-1222]

[2]Locationinpatent:experimentalpartSangwan,PayareL.;Koul,JawahirL.;Koul,Surrinder;Reddy,MallepallyV.;Thota,Niranjan;Khan,InshadA.;Kumar,Ashwani;Kalia,NitinP.;Qazi,GhulamN.[BioorganicandMedicinalChemistry,2008,vol.16,#22,p.9847-9857]

[3]Locationinpatent:experimentalpartCorrea,EdwinAndrés;Högestätt,EdwardD.;Sterner,Olov;Echeverri,Fernando;Zygmunt,PeterM.[BioorganicandMedicinalChemistry,2010,vol.18,#9,p.3299-3306]

[4]Locationinpatent:experimentalpartPedersen,MikaelE.;Metzler,Bjorn;Stafford,GaryI.;VanStaden,Johannes;Jaeger,AnnaK.;Rasmussen,HasseB.[Molecules,2009,vol.14,#9,p.3833-3843]

[5]Ribeiro,TatianaSantana;Freire-De-Lima,Leonardo;Previato,JoseOsvaldo;Mendonca-Previato,Lucia;Heise,Norton;DeLima,MarcoEdilsonFreire[BioorganicandMedicinalChemistryLetters,2004,vol.14,#13,p.3555-3558]

[6]Venkatasamy,Radhakrishnan;Faas,Laura;Young,AntonyR.;Raman,Amala;Hider,RobertC.[BioorganicandMedicinalChemistry,2004,vol.12,#8,p.1905-1920]

[7]Nakamura,Norio;Kiuchi,Fumiyuki;Tsuda,Yoshisuke[Chemicalandpharmaceuticalbulletin,1988,vol.36,#7,p.2647-2651]

[8]Jain,A.K.;Sharma,N.D.;Gupta,S.R.[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1986,vol.25,p.979]

[9]Ablordeppey,SethY.;Fischer,JamesB.;Glennon,RichardA.[BioorganicandMedicinalChemistry,2000,vol.8,#8,p.2105-2111]

[10]Locationinpatent:schemeortableMu,Li-Hua;Wang,Bo;Ren,Hao-Yang;Liu,Ping;Guo,Dai-Hong;Wang,Fu-Meng;Bai,Lin;Guo,Yan-Shen[BioorganicandMedicinalChemistryLetters,2012,vol.22,#9,p.3343-3348]

[11]Fokoue;Marques;Correia;Yamaguchi;Qu;Aires-De-Sousa;Scotti;Lopes;Kato[RSCAdvances,2018,vol.8,#38,p.21407-21413]

[12]CurrentPatentAssignee:CIPLALTD-WO2019/73491,2019,A1Locationinpatent:Page/Pagecolumn9;15

110-89-4   
C15H18O6 
  23434-88-0 

[1]Kiuchi,Fumiyuki;Nakamura,Norio;Saito,Makiko;Komagome,Kazue;Hiramatsu,Hirokuni;Takimoto,Noriaki;Akao,Nobuaki;Kondo,Kaoru;Tsuda,Yoshisuke[ChemicalandPharmaceuticalBulletin,1997,vol.45,#4,p.685-696]

94-62-2    23434-88-0   
(E)-5-(benzod1,3dioxol-5-yl)-1-(piperidin-1-yl)pent-4-en-1-one 

[1]Das,Biswanath;Kashinatham;Madhusudhan[TetrahedronLetters,1998,vol.39,#7,p.677-678]

Literature fold

Title: Synthesis and inhibitory effect of piperine derivates on monoamine oxidase.

Journal: Bioorganic & medicinal chemistry letters20120501

Title: In vitro TRPV1 activity of piperine derived amides.

Journal: Bioorganic & medicinal chemistry20100501

Title: Piperine analogs as potent Staphylococcus aureus NorA efflux pump inhibitors.

Journal: Bioorganic & medicinal chemistry20081115

Title: Madhusudhan P, et al. Tetrahydropiperine, the first natural aryl pentanamide from Piper longum. Biochem Syst Ecol. 2001 May;29(5):537-538.

Title: Koul S, et al. Structure-activity relationship of piperine and its synthetic analogues for their inhibitory potentials of rat hepatic microsomal constitutive and inducible cytochromeP450 activities. Bioorg Med Chem. 2000 Jan;8(1):251-68.

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