Home Aldehydes 2092-49-1
2092-49-1,MFCD00156888
Catalog No.:AA002K0Z

2092-49-1 | 6,6'-Dihydroxy-5,5'-dimethoxybiphenyl-3,3'-dicarbaldehyde

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100mg
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250mg
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1g
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5g
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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:
AA002K0Z
Chemical Name:
6,6'-Dihydroxy-5,5'-dimethoxybiphenyl-3,3'-dicarbaldehyde
CAS Number:
2092-49-1
Molecular Formula:
C16H14O6
Molecular Weight:
302.2788
MDL Number:
MFCD00156888
SMILES:
COc1cc(C=O)cc(c1O)c1cc(C=O)cc(c1O)OC
NSC Number:
16723
FEMA Number:
4107
Properties
Computed Properties
 
Complexity:
351  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
1.7  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1898,vol.20,p.316

[2]AmericanChemicalJournal,1900,vol.24,p.176

[1]BioorganicandMedicinalChemistry,2005,vol.13,#7,p.2537-2546

[2]EuropeanJournalofOrganicChemistry,2013,#1,p.173-179

[3]Patent:JP2017/14122,2017,A,.Locationinpatent:Paragraph0051

[4]JournalofMolecularCatalysisB:Enzymatic,2016,vol.125,p.34-41

[5]JournalofMedicinalChemistry,2008,vol.51,#11,p.3171-3181

[6]AntioxidantsandRedoxSignaling,2011,vol.14,#11,p.2093-2106

[7]GreenChemistry,2012,vol.14,#9,p.2395-2397

[8]AminoAcids,2013,vol.45,#2,p.327-338

[9]TetrahedronLetters,2015,vol.56,#26,p.3988-3991

[10]LettersinOrganicChemistry,2018,vol.15,#8,p.659-664

[11]RSCAdvances,2017,vol.7,#80,p.50459-50471

[12]CanadianJournalofChemistry,2002,vol.80,#9,p.1223-1231

[13]Heterocycles,1992,vol.33,#2,p.641-648

[14]GreenChemistry,2015,vol.17,#11,p.4980-4990

[15]PLoSONE,2017,vol.12,#6,

[16]Bioscience,BiotechnologyandBiochemistry,1999,vol.63,#2,p.390-394

[17]JournalofMedicinalChemistry,2000,vol.43,#8,p.1550-1562

[18]EuropeanJournalofMedicinalChemistry,2018,vol.155,p.623-638

[19]OrganicandBiomolecularChemistry,2008,vol.6,#6,p.XX787-796

[20]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1901,vol.<5>10I,p.100

[21]ChemischeBerichte,1901,vol.34,p.1539

[22]ChemischeBerichte,1902,vol.35,p.3596

[23]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1902,vol.<5>11II,p.149

[24]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1911,vol.<5>20II,p.717,720

[25]ChemischeBerichte,1885,vol.18,p.3493

[26]ChemischeBerichte,1901,vol.34,p.1540

[27]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1901,vol.<5>10I,p.101

[28]ChemischesZentralblatt,1904,p.I,586

[29]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1911,vol.<5>20II,p.717,720

[30]JournalfuerPraktischeChemie(Leipzig),1916,vol.<2>93,p.4

[31]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1911,vol.73,p.258

[32]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1911,vol.73,p.247

[33]JournaldePharmacieetdeChimie,1923,vol.<7>28,p.258

[34]Chem.Zentralbl.,1924,vol.95,#I,p.221

[35]ChemischeBerichte,1902,vol.35,p.3596

[36]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1902,vol.<5>11II,p.149

[37]Chemosphere,1995,vol.30,#5,p.891-906

[38]OrganicLetters,2004,vol.6,#12,p.1975-1978

[39]JournalofAgriculturalandFoodChemistry,2009,vol.57,#18,p.8357-8365

[40]BiochimicaetBiophysicaActa-GeneralSubjects,2011,vol.1810,#2,p.170-177

[41]Polyhedron,2016,vol.117,p.80-89

[42]JournalofAgriculturalandFoodChemistry,2017,vol.65,#11,p.2299-2306

[1]Bioorganicandmedicinalchemistry,2002,vol.10,#10,p.3361-3365

[1]RSCAdvances,2017,vol.7,#80,p.50459-50471

[1]RSCAdvances,2017,vol.7,#80,p.50459-50471

Downstream Synthesis Route

[1]Patent:US10155969,2018,B2.Locationinpatent:Page/Pagecolumn24;25

[2]ActaChemicaScandinavica(1947),1955,vol.9,p.319,332

[3]Chemosphere,2000,vol.40,p.115-124

[1]JournaloftheAmericanPharmaceuticalAssociation(1912),1952,vol.41,p.348,349

[1]ChemischeBerichte,1885,vol.18,p.3493

[1]JournaloftheChemicalSocietyC:Organic,1968,vol.<C>,p.83-85

[2]JournaloftheChemicalSocietyC:Organic,1970,p.865-872

[1]BioorganicandMedicinalChemistry,2005,vol.13,p.2537-2546

Literature

Title: Development of novel antiatherogenic biaryls: design, synthesis, and reactivity.

Journal: Journal of medicinal chemistry 20080612

Title: Characterization of the 5-carboxyvanillate decarboxylase gene and its role in lignin-related biphenyl catabolism in Sphingomonas paucimobilis SYK-6.

Journal: Applied and environmental microbiology 20020901

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SDS
Tags:2092-49-1 Molecular Formula|2092-49-1 MDL|2092-49-1 SMILES|2092-49-1 6,6'-Dihydroxy-5,5'-dimethoxybiphenyl-3,3'-dicarbaldehyde