Home Nitros 2-Chloro-4-nitrophenol

2-Chloro-4-nitrophenol

CAS No.:
619-08-9
Catalog Number:
AG003GXO
Molecular Formula:
C6H4ClNO3
Molecular Weight:
173.5539
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$63
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG003GXO
Chemical Name:
2-Chloro-4-nitrophenol
CAS Number:
619-08-9
Molecular Formula:
C6H4ClNO3
Molecular Weight:
173.5539
MDL Number:
MFCD00043910
IUPAC Name:
2-chloro-4-nitrophenol
InChI:
InChI=1S/C6H4ClNO3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H
InChI Key:
BOFRXDMCQRTGII-UHFFFAOYSA-N
SMILES:
[O-][N+](=O)c1ccc(c(c1)Cl)O
EC Number:
210-578-8
UNII:
Y2V03M9UL8
NSC Number:
1316
Properties
Complexity:
158  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
172.988g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
173.552g/mol
Monoisotopic Mass:
172.988g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
66A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3  
Literature
Title Journal
Novel fluorescence method for detection of α-L-fucosidase based on CdTe quantum dots. Analytical chemistry 20120501
Chemotaxis of Burkholderia sp. strain SJ98 towards chloronitroaromatic compounds that it can metabolise. BMC microbiology 20120101
Metabolism of 2-chloro-4-nitrophenol in a gram negative bacterium, Burkholderia sp. RKJ 800. PloS one 20120101
High-throughput colorimetric assays for nucleotide sugar formation and glycosyl transfer. Methods in enzymology 20120101
Pathway for degradation of 2-chloro-4-nitrophenol in Arthrobacter sp. SJCon. Current microbiology 20111201
Reductive dehalogenation mediated initiation of aerobic degradation of 2-chloro-4-nitrophenol (2C4NP) by Burkholderia sp. strain SJ98. Applied microbiology and biotechnology 20111101
Using simple donors to drive the equilibria of glycosyltransferase-catalyzed reactions. Nature chemical biology 20111001
Structure and activity of Paenibacillus polymyxa xyloglucanase from glycoside hydrolase family 44. The Journal of biological chemistry 20110930
Predicting mixture toxicity of seven phenolic compounds with similar and dissimilar action mechanisms to Vibrio qinghaiensis sp.nov.Q67. Ecotoxicology and environmental safety 20110901
Potentiometric determination of α-L-fucosidase enzyme by using 2-chloro-4-nitrophenol-rhodamine B ion pair chemical recognition in PVC membrane sensor. Analytical and bioanalytical chemistry 20110501
Novel spectrofluorimetric method for measuring the activity of the enzyme alpha-L-fucosidase using the nano composite optical sensor samarium(III)-doxycycline complex doped in sol-gel matrix. Analytical chemistry 20100715
Effect of GaAlAs laser irradiation on enzyme activity. Photomedicine and laser surgery 20100601
Degradation of 4-nitrophenol, 2-chloro-4-nitrophenol, and 2,4-dinitrophenol by Rhodococcus imtechensis strain RKJ300. Environmental science & technology 20100201
Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starch. PloS one 20100101
Spectrofluorimetric method for measuring the activity of the enzyme alpha-L-fucosidase using the ion associate of 2-chloro-4-nitro phenol-rhodamine-B. Talanta 20091115
2-Chloro-1-(3-fluoro-benz-yloxy)-4-nitro-benzene. Acta crystallographica. Section E, Structure reports online 20091001
Thermophilic degradation of phenolic compounds in lab scale hybrid up flow anaerobic sludge blanket reactors. Journal of hazardous materials 20090530
Analysis of urinary N-acetyl-beta-D-glucosaminidase using 2,4-dinitrophenyl-1-thio N-acetyl-beta-D-glucosaminide as the substrate. Journal of clinical laboratory analysis 20030101
Comparative molecular field analysis of substrates for an aryl sulfotransferase based on catalytic mechanism and protein homology modeling. Journal of medicinal chemistry 20021205
Properties