Catalog No.:AA0032ZD

7170-36-7 | 2,6-Pyridinedicarboxylic acid monomethyl ester

Name: Name:2,6-Pyridinedicarboxylic acid monomethyl ester
Brand: AABLOCKS
SKU: AA0032ZD
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0032ZD

Chemical Name:

2,6-Pyridinedicarboxylic acid monomethyl ester

CAS Number:

7170-36-7

Molecular Formula:

C8H7NO4

Molecular Weight:

181.1455

MDL Number:

MFCD00806109

SMILES:

COC(=O)c1cccc(n1)C(=O)O

Properties

BP:

392.7°C at 760 mmHg

Form:

Solid

MP:

144-146 °C

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

216

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.9

Upstream Synthesis Route

5453-67-8

7170-36-7

[1]SyntheticCommunications,1995,vol.25,#5,p.739-742

[2]BioorganicandMedicinalChemistryLetters,2017,vol.27,#15,p.3486-3489

[3]Tetrahedron,1997,vol.53,#37,p.12405-12414

[4]JournalofMedicinalChemistry,2017,vol.60,#17,p.7267-7283

[5]JournalofMedicinalChemistry,2018,vol.61,#14,p.6400-6400

[6]ChemicalCommunications,2011,vol.47,#22,p.6416-6418

[7]OrganicLetters,2011,vol.13,#12,p.3194-3197

[8]OrganicandBiomolecularChemistry,2012,vol.10,#6,p.1172-1180

[9]Chemistry-AEuropeanJournal,2015,vol.21,#26,p.9493-9504

[10]AngewandteChemie-InternationalEdition,2016,vol.55,#41,p.12668-12672

[11]Angew.Chem.,2016,vol.128,#41,p.12859-12863,5

[12]DaltonTransactions,2016,vol.45,#47,p.19024-19033

[13]JournaloftheKoreanChemicalSociety,2013,vol.57,#5,p.591-598

[14]Patent:US2009/203657,2009,A1,.Locationinpatent:Page/Pagecolumn72

[15]Chemistry-AEuropeanJournal,2005,vol.11,#4,p.1109-1118

[16]SpectrochimicaActa,PartA:MolecularandBiomolecularSpectroscopy,2012,vol.98,p.170-177,8

[17]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2012,vol.98,p.170-177

[18]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2015,vol.135,p.953-958

[19]JournaloftheAmericanChemicalSociety,2003,vol.125,#1,p.296-304

[20]JournalofMedicinalChemistry,1987,vol.30,#10,p.1918-1928

[21]TetrahedronLetters,2007,vol.48,#45,p.7990-7993

[22]InorganicChemistry,2015,vol.54,#10,p.4611-4620

67-56-1

499-83-2

7170-36-7

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,#3,p.1025-1040

[2]InorganicChemistry,2012,vol.51,#18,p.10012-10024

[3]JournaloftheAmericanChemicalSociety,2011,vol.133,#40,p.16219-16234

[4]Chemistry-AEuropeanJournal,2016,vol.22,#24,p.8113-8123

[5]DaltonTransactions,2015,vol.44,#6,p.2529-2540

[6]ChemMedChem,2012,vol.7,#10,p.1825-1839

[7]Patent:WO2006/117754,2006,A1,.Locationinpatent:Page/Pagecolumn50-51

67-56-1

3739-94-4

5453-67-8

7170-36-7

[1]Tetrahedron,2011,vol.67,#44,p.8458-8464

499-83-2

7170-36-7

[1]Chemistry-AEuropeanJournal,2005,vol.11,#4,p.1109-1118

[2]JournaloftheAmericanChemicalSociety,2003,vol.125,#1,p.296-304

[3]Tetrahedron,1997,vol.53,#37,p.12405-12414

[4]JournalofMedicinalChemistry,1987,vol.30,#10,p.1918-1928

[5]ChemicalCommunications,2011,vol.47,#22,p.6416-6418

[6]OrganicLetters,2011,vol.13,#12,p.3194-3197

[7]Tetrahedron,2011,vol.67,#44,p.8458-8464

[8]OrganicandBiomolecularChemistry,2012,vol.10,#6,p.1172-1180

[9]SpectrochimicaActa,PartA:MolecularandBiomolecularSpectroscopy,2012,vol.98,p.170-177,8

[10]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2012,vol.98,p.170-177

[11]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2015,vol.135,p.953-958

[12]InorganicChemistry,2015,vol.54,#10,p.4611-4620

[13]Chemistry-AEuropeanJournal,2015,vol.21,#26,p.9493-9504

[14]DaltonTransactions,2016,vol.45,#47,p.19024-19033

[15]JournalofMedicinalChemistry,2017,vol.60,#17,p.7267-7283

67-56-1

499-83-2

5453-67-8

7170-36-7

[1]JournalofOrganicChemistry,1981,vol.46,#24,p.4914-4920

[2]JournalofOrganometallicChemistry,1980,vol.186,#2,p.147-153

Downstream Synthesis Route

69950-65-8

7170-36-7

[1]ChemischeBerichte,1953,vol.86,p.584,587

7170-36-7

3014-80-0

849669-86-9

[1]Chemistry-AEuropeanJournal,2005,vol.11,p.1109-1118

53710-17-1

7170-36-7

[1]JournalofOrganometallicChemistry,1980,vol.186,p.147-153

13602-11-4

7170-36-7

[1]ChemischeBerichte,1953,vol.86,p.584,587

67-56-1

499-83-2

7170-36-7

[1]Canard,Gabriel;Koeller,Sylvain;Bernardinelli,Gerald;Piguet,Claude[JournaloftheAmericanChemicalSociety,2008,vol.130,#3,p.1025-1040]

[2]Ryan,PatrickE.;Canard,Gabriel;Koeller,Sylvain;Bocquet,Bernard;Piguet,Claude[InorganicChemistry,2012,vol.51,#18,p.10012-10024]

[3]Lemonnier,Jean-Francois;Guenee,Laure;Beuchat,Cesar;Wesolowski,TomaszA.;Mukherjee,Prasun;Waldeck,DavidH.;Gogick,KristyA.;Petoud,Stephane;Piguet,Claude[JournaloftheAmericanChemicalSociety,2011,vol.133,#40,p.16219-16234]

[4]Babel,Lucille;Hoang,ThiNhuY;Guénée,Laure;Besnard,Céline;Wesolowski,TomaszA.;Humbert-Droz,Marie;Piguet,Claude[Chemistry-AEuropeanJournal,2016,vol.22,#24,p.8113-8123]

[5]Babel,Lucille;Baudet,Karine;Besnard,Céline;Kale,Vishal;Mirzakhani,Mohsen;Naseri,Soroush;Nozary,Homayoun;Piguet,Claude[InorganicChemistry,2020,vol.59,#1,p.62-75]

[6]Zare,Davood;Suffren,Yan;Gune,Laure;Eliseeva,SvetlanaV.;Nozary,Homayoun;Aboshyan-Sorgho,Lilit;Petoud,Stphane;Hauser,Andreas;Piguet,Claude[DaltonTransactions,2015,vol.44,#6,p.2529-2540]

[7]Aiello,Francesca;Shabaik,Yumna;Esqueda,Adrian;Sanchez,TinoW.;Grande,Fedora;Garofalo,Antonio;Neamati,Nouri[ChemMedChem,2012,vol.7,#10,p.1825-1839]

[8]CurrentPatentAssignee:SUNPHARMACEUTICALINDUSTRIESLIMITED-WO2006/117754,2006,A1Locationinpatent:Page/Pagecolumn50-51

Literature

Title: Penipratynolene, a novel nematicide from penicillium bilaiae Chalabuda.

Journal: Bioscience, biotechnology, and biochemistry 20040101

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