Name: Name:2,3-Dihydroxy-benzenepropanoic acid
Brand: AABLOCKS
SKU: AA00C949
Rating: 90 (10 reviews)

Technical Information

Catalog Number: AA00C949

Chemical Name: 2,3-Dihydroxy-benzenepropanoic acid

CAS Number: 3714-73-6

Molecular Formula: C9H10O4

Molecular Weight: 182.1733

MDL Number: MFCD12923244

SMILES: OC(=O)CCc1cccc(c1O)O

Properties

Form: Solid

MP: 118-122°C

Storage: Keep in dry area;2-8℃;Inert atmosphere;

Complexity: 181

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 13

Hydrogen Bond Acceptor Count: 4

Hydrogen Bond Donor Count: 3

Isotope Atom Count: 0

Rotatable Bond Count: 3

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 1

Downstream Synthesis Route

3714-73-6

(2Z,4E)-2-Hydroxy-6-oxo-nona-2,4-dienedioicacid

[1]Lam,WinnieW.Y.;Bugg,TimothyD.H.[JournaloftheChemicalSociety.Chemicalcommunications,1994,#10,p.1163-1164]

67-56-1

3714-73-6

2-hydroxy-6-oxo-nona-2,4-diene1,9-dioicacid1methylester

[1]Lin;Reid;Bugg[JournaloftheAmericanChemicalSociety,2001,vol.123,#21,p.5030-5039]

[2]Lin;Reid;Bugg[JournaloftheAmericanChemicalSociety,2001,vol.123,#21,p.5030-5039]

3714-73-6

8-hydroxy-chroman-2-one

[1]Mendel,Sharon;Arndt,Andrew;Bugg,TimothyD.H.[ChemicalCommunications,2005,#5,p.666-668]

Literature fold

Title: Biomimetic formation of 2-tropolones by dioxygenase-catalysed ring expansion of substituted 2,4-cyclohexadienones.

Journal: Chembiochem : a European journal of chemical biology20100125

Title: The complete multipartite genome sequence of Cupriavidus necator JMP134, a versatile pollutant degrader.

Journal: PloS one20100101

Title: Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function.

Journal: PloS one20100101

Title: Degradation of chloroaromatics by Pseudomonas putida GJ31: assembled route for chlorobenzene degradation encoded by clusters on plasmid pKW1 and the chromosome.

Journal: Microbiology (Reading, England)20091201

Title: 3-Hydroxyphenylpropionate and phenylpropionate are synergistic activators of the MhpR transcriptional regulator from Escherichia coli.

Journal: The Journal of biological chemistry20090807

Title: Metabolic reconstruction of aromatic compounds degradation from the genome of the amazing pollutant-degrading bacterium Cupriavidus necator JMP134.

Journal: FEMS microbiology reviews20080801

Title: Exploiting the pathway structure of metabolism to reveal high-order epistasis.

Journal: BMC systems biology20080101

Title: Directed evolution of a non-heme-iron-dependent extradiol catechol dioxygenase: identification of mutants with intradiol oxidative cleavage activity.

Journal: Chembiochem : a European journal of chemical biology20061201

Title: Xenobiotic reductase A in the degradation of quinoline by Pseudomonas putida 86: physiological function, structure and mechanism of 8-hydroxycoumarin reduction.

Journal: Journal of molecular biology20060804

Title: 3-phenylpropionate catabolism and the Escherichia coli oxidative stress response.

Journal: Research in microbiology20050401

Title: Lactone synthesis activity in a site-directed mutant of an extradiol catechol dioxygenase enzyme.

Journal: Chemical communications (Cambridge, England)20050207

Title: Acid-base catalysis in the extradiol catechol dioxygenase reaction mechanism: site-directed mutagenesis of His-115 and His-179 in Escherichia coli 2,3-dihydroxyphenylpropionate 1,2-dioxygenase (MhpB).

Journal: Biochemistry20041026

Title: Extradiol oxidative cleavage of catechols by ferrous and ferric complexes of 1,4,7-triazacyclononane: insight into the mechanism of the extradiol catechol dioxygenases.

Journal: Journal of the American Chemical Society20010530

3714-73-6 | 2,3-Dihydroxy-benzenepropanoic acid