Home Carboxes 3714-73-6
3714-73-6,MFCD12923244
Catalog No.:AA00C949

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

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$445.00   $312.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
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
Properties
 
Form:
Solid  
MP:
118-122°C  
Storage:
Keep in dry area;2-8℃;Inert atmosphere;  

Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
3  
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

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

Journal: Chembiochem : a European journal of chemical biology 20100125

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

Journal: PloS one 20100101

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

Journal: PloS one 20100101

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 chemistry 20090807

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

Journal: FEMS microbiology reviews 20080801

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

Journal: BMC systems biology 20080101

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 biology 20061201

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 biology 20060804

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

Journal: Research in microbiology 20050401

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: Biochemistry 20041026

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 Society 20010530

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:3714-73-6 Molecular Formula|3714-73-6 MDL|3714-73-6 SMILES|3714-73-6 2,3-Dihydroxy-benzenepropanoic acid