626-06-2,MFCD00129028
Catalog No.:AA003G22

626-06-2 | 2,6-Dihydroxypyridine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$13.00   $9.00
- +
1g
95%
in stock  
$52.00   $36.00
- +
5g
95%
in stock  
$205.00   $143.00
- +
10g
95%
in stock  
$394.00   $276.00
- +
25g
>97%
in stock  
$978.00   $685.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003G22
Chemical Name:
2,6-Dihydroxypyridine
CAS Number:
626-06-2
Molecular Formula:
C5H5NO2
Molecular Weight:
111.0987
MDL Number:
MFCD00129028
SMILES:
Oc1cccc(n1)O
Properties
Properties
 
BP:
387.2°C at 760 mmHg  
Form:
Solid  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
169  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.1  

Literature

Title: Azo-hydrazone tautomerism observed from UV-vis spectra by pH control and metal-ion complexation for two heterocyclic disperse yellow dyes.

Journal: Dalton transactions (Cambridge, England : 2003) 20120828

Title: Purification, characterization, and cloning of a bifunctional molybdoenzyme with hydratase and alcohol dehydrogenase activity.

Journal: Applied microbiology and biotechnology 20110301

Title: The role of system-specific molecular chaperones in the maturation of molybdoenzymes in bacteria.

Journal: Biochemistry research international 20110101

Title: 4-(4-Methoxy-phen-yl)-1-phenyl-pyridine-2,6(1H,3H)-dione.

Journal: Acta crystallographica. Section E, Structure reports online 20090601

Title: Structure of 2,6-dihydroxypyridine 3-hydroxylase from a nicotine-degrading pathway.

Journal: Journal of molecular biology 20080523

Title: Two closely related pathways of nicotine catabolism in Arthrobacter nicotinovorans and Nocardioides sp. strain JS614.

Journal: Archives of microbiology 20080501

Title: An azo dye molecule having a pyridine-2,6-dione backbone.

Journal: Acta crystallographica. Section C, Crystal structure communications 20060201

Title: Encapsulated guest molecules in the dimer of octahydroxypyridine[4]arene.

Journal: Journal of the American Chemical Society 20040811

Title: A new type of calixarene: octahydroxypyridin.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20010119

Title: Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.

Journal: Biochemical pharmacology 19940817

Title: The bacterial oxidation of nicotine. VII. Partial purification and properties of 2,6-dihydroxypyridine oxidase.

Journal: The Journal of biological chemistry 19721210

Title: The bacterial oxidation of nicotine. VI. The metabolism of 2,6-dihydroxypseudooxynicotine.

Journal: The Journal of biological chemistry 19650901

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SDS
Related Products of 626-06-2
Tags:626-06-2 Molecular Formula|626-06-2 MDL|626-06-2 SMILES|626-06-2 2,6-Dihydroxypyridine
Catalog No.: AA003G22
626-06-2,MFCD00129028
626-06-2 | 2,6-Dihydroxypyridine
Pack Size: 100mg
Purity: 97%
in stock
$13.00 $9.00
Pack Size: 1g
Purity: 95%
in stock
$52.00 $36.00
Pack Size: 5g
Purity: 95%
in stock
$205.00 $143.00
Pack Size: 10g
Purity: 95%
in stock
$394.00 $276.00
Pack Size: 25g
Purity: >97%
in stock
$978.00 $685.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003G22
Chemical Name: 2,6-Dihydroxypyridine
CAS Number: 626-06-2
Molecular Formula: C5H5NO2
Molecular Weight: 111.0987
MDL Number: MFCD00129028
SMILES: Oc1cccc(n1)O
Properties
BP: 387.2°C at 760 mmHg  
Form: Solid  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 169  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.1  
Literature fold

Title: Azo-hydrazone tautomerism observed from UV-vis spectra by pH control and metal-ion complexation for two heterocyclic disperse yellow dyes.

Journal: Dalton transactions (Cambridge, England : 2003)20120828

Title: Purification, characterization, and cloning of a bifunctional molybdoenzyme with hydratase and alcohol dehydrogenase activity.

Journal: Applied microbiology and biotechnology20110301

Title: The role of system-specific molecular chaperones in the maturation of molybdoenzymes in bacteria.

Journal: Biochemistry research international20110101

Title: 4-(4-Methoxy-phen-yl)-1-phenyl-pyridine-2,6(1H,3H)-dione.

Journal: Acta crystallographica. Section E, Structure reports online20090601

Title: Structure of 2,6-dihydroxypyridine 3-hydroxylase from a nicotine-degrading pathway.

Journal: Journal of molecular biology20080523

Title: Two closely related pathways of nicotine catabolism in Arthrobacter nicotinovorans and Nocardioides sp. strain JS614.

Journal: Archives of microbiology20080501

Title: An azo dye molecule having a pyridine-2,6-dione backbone.

Journal: Acta crystallographica. Section C, Crystal structure communications20060201

Title: Encapsulated guest molecules in the dimer of octahydroxypyridine[4]arene.

Journal: Journal of the American Chemical Society20040811

Title: A new type of calixarene: octahydroxypyridin.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20010119

Title: Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.

Journal: Biochemical pharmacology19940817

Title: The bacterial oxidation of nicotine. VII. Partial purification and properties of 2,6-dihydroxypyridine oxidase.

Journal: The Journal of biological chemistry19721210

Title: The bacterial oxidation of nicotine. VI. The metabolism of 2,6-dihydroxypseudooxynicotine.

Journal: The Journal of biological chemistry19650901

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