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Home Amines 6264-93-3
6264-93-3,MFCD01734302
Catalog No.:AA00EKWZ

6264-93-3 | 2-Amino-2,4,6-cycloheptatrien-1-one

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100mg
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$180.00   $126.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00EKWZ
Chemical Name:
2-Amino-2,4,6-cycloheptatrien-1-one
CAS Number:
6264-93-3
Molecular Formula:
C7H7NO
Molecular Weight:
121.1366
MDL Number:
MFCD01734302
SMILES:
Nc1cccccc1=O
Properties
Computed Properties
 
Complexity:
211  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.2  

Downstream Synthesis Route

[1]Doering;Knox[JournaloftheAmericanChemicalSociety,1951,vol.73,p.828,838]Nozoeetal.[Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1952,vol.<I>36,p.126,146][Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1953,vol.<I>37,p.407,419]

[1]Doering,vonE.;Hiskey[JournaloftheAmericanChemicalSociety,1952,vol.74,p.5688,5693]Nozoeetal.[Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1952,vol.<I>36,p.126,146][Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1953,vol.<I>37,p.407,419]

[2]Nozoe,T.etal.[BulletinoftheChemicalSocietyofJapan,1968,vol.41,p.2978-2984]

[1]Doering,vonE.;Hiskey[JournaloftheAmericanChemicalSociety,1952,vol.74,p.5688,5693]Nozoeetal.[Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1952,vol.<I>36,p.126,146][Sci.Rep.TohokuUniv.,Ser.1:Phys.,Chem.,Astron.,1953,vol.<I>37,p.407,419]

[1]Ohtsu,Keito;Hayami,Ryohei;Sagawa,Takuya;Tsukada,Satoru;Yamamoto,Kazuki;Gunji,Takahiro[Tetrahedron,2019,vol.75,#46]

[2]Nagahara;Nakano;Mimura;Nakamura;Uchida[ChemicalandPharmaceuticalBulletin,1994,vol.42,#12,p.2491-2499]

[3]Nozoeetal.[Chemistryandindustry,1954,p.1357]

[4]CurrentPatentAssignee:PFIZERINC-US4337265,1982,A

[1]Machiguchi,Takahisa;Kano,Yuichi;Hasegawa,Toshio[ChemistryLetters,1990,#4,p.563-566]

[2]Machiguchi;Hasegawa;Kano[BulletinoftheChemicalSocietyofJapan,1993,vol.66,#12,p.3699-3706]

[3]Soma;Nakazawa;Watanabe;Sato;Sunagawa[Chemicalandpharmaceuticalbulletin,1965,vol.13,#7,p.819-828]

Literature

Title: Hormetic response of cultured normal and tumor cells to 2-aminotropone derivatives.

Journal: In vivo (Athens, Greece) 20100101

Title: Tumor-specific cytotoxicity and type of cell death induced by benzo[b]cyclohept[e][1,4]oxazine and 2-aminotropone derivatives.

Journal: Anticancer research 20090401

Title: Inhibition of NO production in LPS-stimulated mouse macrophage-like cells by benzo[b]cyclohept[e] [1,4]oxazine and 2-aminotropone derivatives.

Journal: In vivo (Athens, Greece) 20090101

Title: Bonding in tropolone, 2-aminotropone, and aminotroponimine: no evidence of resonance-assisted hydrogen-bond effects.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

Title: Crystal structures of 2-aminotropone, n,n'-di(tropon-2-yl)piperazine, and 5-(4-ethoxyphenylazo)tropolone.

Journal: Journal of oleo science 20080101

Title: Electrospray mass spectrometry of 2-aminotroponimines and 2-aminotropones.

Journal: European journal of mass spectrometry (Chichester, England) 20030101

Title: Cytotoxic activity of tropolones against human oral tumor cell lines.

Journal: Anticancer research 20030101

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