Catalog No.:AA00EIG4

606-19-9 | 2-Hydroxybenzene-1,3-dicarboxylic acid

Name: Name:2-Hydroxybenzene-1,3-dicarboxylic acid
Brand: AABLOCKS
SKU: AA00EIG4
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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:

AA00EIG4

Chemical Name:

2-Hydroxybenzene-1,3-dicarboxylic acid

CAS Number:

606-19-9

Molecular Formula:

C8H6O5

Molecular Weight:

182.1302

MDL Number:

MFCD01717559

SMILES:

OC(=O)c1cccc(c1O)C(=O)O

NSC Number:

252689

Properties

BP:

275.5°C (rough estimate)

Form:

Solid

MP:

244°C

Refractive Index:

1.5690 (estimate)

Computed Properties

Complexity:

203

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.1

Downstream Synthesis Route

83-40-9

606-19-9

[1]Patent:WO2017/222921,2017,A1.Locationinpatent:Paragraph0027;0043-0045

[2]Chemistry-AEuropeanJournal,2018,vol.24,p.14824-14829

[3]JournalofInorganicBiochemistry,2016,vol.162,p.263-273

[4]ChemischeBerichte,1906,vol.39,p.799

[5]JournaloftheAmericanPharmaceuticalAssociation(1912),1945,vol.34,p.42

[6]Chemicalandpharmaceuticalbulletin,1969,vol.17,p.1279-1283

1951-38-8

606-19-9

[1]OrganicLetters,2019,vol.21,p.1999-2003

[2]Patent:US6555556,2003,B1

[3]DaltonTransactions,2014,vol.43,p.12989-12995

[4]Patent:WO2014/78690,2014,A1.Locationinpatent:Paragraph00184

[5]ChemicalCommunications,2017,vol.53,p.625-628

[6]ChemicalCommunications,2017,vol.53,p.5322-5325

[7]ChemischeBerichte,1879,vol.12,p.818,821

[8]ChemischeBerichte,1879,vol.12,p.818,821

[9]JournaloftheAmericanChemicalSociety,1950,vol.72,p.1982,1983

[10]JournaloftheAmericanChemicalSociety,2004,vol.126,p.9484-9485

[11]Patent:US2005/54604,2005,A1.Locationinpatent:Page/Pagecolumn7

[12]ChemPlusChem,2016,vol.81,p.526-534

606-19-9

77-78-1

1951-38-8

[1]ChemischeBerichte,1906,vol.39,p.799

56-23-5

69-72-7

606-19-9

636-46-4

[1]ChemischeBerichte,1877,vol.10,p.2190

[2]Patent:DE258887, Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.11,p.208

69-72-7

606-19-9

636-46-4

[1]ChemischeBerichte,1877,vol.10,p.2190

[2]Patent:DE258887, Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.11,p.208

Literature

Title: A flexible copper based microporous metal-organic framework displaying selective adsorption of hydrogen over nitrogen.

Journal: Dalton transactions (Cambridge, England : 2003) 20110407

Title: A mixed-valence copper coordination polymer generated by a hydrothermal metal/ligand redox reaction process.

Journal: Acta crystallographica. Section C, Crystal structure communications 20081001

Title: Efficient near-UV photosensitization of the Tb(III) green luminescence by use of 2-hydroxyisophthalate ligands.

Journal: Dalton transactions (Cambridge, England : 2003) 20080628

Title: Hydrothermal syntheses, crystal structures and magnetic properties of two copper(II) complexes involved in situ ligand synthesis.

Journal: Dalton transactions (Cambridge, England : 2003) 20070728

Title: Designer ligands for beryllium.

Journal: Journal of the American Chemical Society 20040811

Title: 2-Hydroxyisophthalic acid: hydrogen-bonding patterns in the monohydrate and the tetraphenylphosphonium salt. An instance of dramatic acidity enhancement by symmetric, internally hydrogen-bonded anion stabilization.

Journal: Acta crystallographica. Section B, Structural science 20040801

Title: A mixed-valence copper coordination polymer generated by hydrothermal metal/ligand redox reactions.

Journal: Chemical communications (Cambridge, England) 20020707

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