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619-10-3,MFCD01571825
Catalog No.:AA00335Q

619-10-3 | 2-Chloro-5-nitrophenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$9.00   $7.00
- +
10g
98%
in stock  
$17.00   $12.00
- +
100g
98%
in stock  
$102.00   $71.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00335Q
Chemical Name:
2-Chloro-5-nitrophenol
CAS Number:
619-10-3
Molecular Formula:
C6H4ClNO3
Molecular Weight:
173.5539
MDL Number:
MFCD01571825
SMILES:
[O-][N+](=O)c1ccc(c(c1)O)Cl
NSC Number:
212119
Properties
Properties
 
BP:
276.1°C at 760 mmHg  
Form:
Solid  
MP:
125-129 C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
158  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.3  

Upstream Synthesis Route

[1]Patent:US2003/100580,2003,A1,

[2]Patent:US2010/160388,2010,A1,.Locationinpatent:Page/Pagecolumn58

[3]Patent:US2010/160389,2010,A1,.Locationinpatent:Page/Pagecolumn49

[4]Patent:US2011/28502,2011,A1,.Locationinpatent:Page/Pagecolumn44-45

[5]Patent:US2011/71143,2011,A1,.Locationinpatent:Page/Pagecolumn36

[6]JournalofMedicinalChemistry,2015,vol.58,#21,p.8413-8426

[7]BioorganicandMedicinalChemistryLetters,2006,vol.16,#3,p.668-671

[8]EnvironmentalToxicologyandChemistry,2001,vol.20,#7,p.1381-1389

[9]BioorganicandMedicinalChemistry,2013,vol.21,#23,p.7398-7405

[10]Patent:WO2007/38387,2007,A2,.Locationinpatent:Page/Pagecolumn24;25

[11]PrzemyslChemiczny,1951,vol.30,p.647

[12]Chem.Abstr.,1952,p.11141

[13]BiochemicalJournal,1956,vol.64,p.38,39

[14]Patent:WO2004/85425,2004,A1,.Locationinpatent:Page110-111

[1]Patent:WO2004/46092,2004,A2,.Locationinpatent:Page50-51

[2]Patent:WO2004/46092,2004,A2,.Locationinpatent:Page53-55

[1]Patent:US2011/9390,2011,A1,.Locationinpatent:Page/Pagecolumn16

[2]Patent:WO2009/130481,2009,A1,.Locationinpatent:Page/Pagecolumn128-129

[3]BioorganicandMedicinalChemistryLetters,2006,vol.16,#3,p.668-671

[4]BioorganicandMedicinalChemistry,2013,vol.21,#23,p.7398-7405

[5]TetrahedronLetters,2005,vol.46,#23,p.4023-4026

[6]Patent:US2013/72482,2013,A1,.Locationinpatent:Paragraph0249;0250

[7]JournaloftheChemicalSociety,1896,vol.69,p.1323

[8]Patent:WO2007/38387,2007,A2,.Locationinpatent:Page/Pagecolumn24;25

[1]Patent:WO2012/9309,2012,A1,.Locationinpatent:Page/Pagecolumn34;35

[2]EnvironmentalToxicologyandChemistry,2001,vol.20,#7,p.1381-1389

[3]Patent:WO2005/49613,2005,A1,.Locationinpatent:Page/Pagecolumn53

[4]JournalfuerPraktischeChemie(Leipzig),1930,vol.<2>127,p.20,22

[5]Tetrahedron,1993,vol.49,#15,p.3053-3064

[6]BioorganicandMedicinalChemistryLetters,2001,vol.11,#5,p.619-622

[7]JournalofMedicinalChemistry,2007,vol.50,#18,p.4351-4373

[8]Patent:WO2004/85425,2004,A1,.Locationinpatent:Page102

[1]Patent:WO2004/46092,2004,A2,.Locationinpatent:Page50-51

[2]Patent:WO2004/46092,2004,A2,.Locationinpatent:Page53-55

Downstream Synthesis Route

[1]Patent:WO2012/9309,2012,A1.Locationinpatent:Page/Pagecolumn34;35

[2]EnvironmentalToxicologyandChemistry,2001,vol.20,p.1381-1389

[3]Patent:WO2005/49613,2005,A1.Locationinpatent:Page/Pagecolumn53

[4]JournalfurpraktischeChemie(Leipzig1954),1930,vol.<2>127,p.20,22

[5]Tetrahedron,1993,vol.49,p.3053-3064

[6]BioorganicandMedicinalChemistryLetters,2001,vol.11,p.619-622

[7]JournalofMedicinalChemistry,2007,vol.50,p.4351-4373

[8]Patent:WO2004/85425,2004,A1.Locationinpatent:Page102

[1]Patent:US2003/100580,2003,A1

[2]Patent:US2010/160388,2010,A1.Locationinpatent:Page/Pagecolumn58

[3]Patent:US2010/160389,2010,A1.Locationinpatent:Page/Pagecolumn49

[4]Patent:US2011/28502,2011,A1.Locationinpatent:Page/Pagecolumn44-45

[5]Patent:US2011/71143,2011,A1.Locationinpatent:Page/Pagecolumn36

[6]JournalofMedicinalChemistry,2015,vol.58,p.8413-8426

[7]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.668-671

[8]EnvironmentalToxicologyandChemistry,2001,vol.20,p.1381-1389

[9]BioorganicandMedicinalChemistry,2013,vol.21,p.7398-7405

[10]Patent:WO2007/38387,2007,A2.Locationinpatent:Page/Pagecolumn24;25

[11]PrzemyslChemiczny,1951,vol.30,p.647    Chem.Abstr.,1952,p.11141

[12]BiochemicalJournal,1956,vol.64,p.38,39

[13]Patent:WO2004/85425,2004,A1.Locationinpatent:Page110-111

[1]Patent:US2011/9390,2011,A1.Locationinpatent:Page/Pagecolumn16

[2]Patent:WO2009/130481,2009,A1.Locationinpatent:Page/Pagecolumn128-129

[3]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.668-671

[4]BioorganicandMedicinalChemistry,2013,vol.21,p.7398-7405

[5]TetrahedronLetters,2005,vol.46,p.4023-4026

[6]Patent:US2013/72482,2013,A1.Locationinpatent:Paragraph0249;0250

[7]JournaloftheChemicalSociety,1896,vol.69,p.1323

[8]Patent:WO2007/38387,2007,A2.Locationinpatent:Page/Pagecolumn24;25

[1]Baker,B.R.;Ashton,W.T.[JournalofMedicinalChemistry,1970,vol.13,#6,p.1149-1154]

[1]JournalofMedicinalChemistry,1970,vol.13,p.1149-1154

[2]Patent:US2005/54850,2005,A1

Literature

Title: Metabolism of 2-chloro-4-nitrophenol in a gram negative bacterium, Burkholderia sp. RKJ 800.

Journal: PloS one 20120101

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

Journal: PloS one 20100101

Title: Kinetics and mechanism of degradation of p-chloronitrobenzene in water by ozonation.

Journal: Journal of hazardous materials 20080415

Title: Urinary metabolites and health effects in workers exposed chronically to chloronitrobenzene.

Journal: Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 20070101

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