Basic Info

Common NameChloromycetny(F01073)
2D Structure
FRCD IDF01073
CAS Number579-51-1
PubChem CID298
FormulaC11H12Cl2N2O5
IUPAC Name

2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide

InChI Key

WIIZWVCIJKGZOK-UHFFFAOYSA-N

InChI

InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)

Canonical SMILES

C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]

Isomeric SMILES

C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]

Synonyms
        
            Tyfomycine
        
            579-51-1
        
            EN300-50870
        
            Chloromycetin Hydrocortisone
        
            Chloromyxin
        
            Mycochlorin
        
            Ocuphenicol
        
            Chlorocin
        
            Levocin
        
            2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
        
Classifies
                

                  
                    Veterinary Drug
                  

                
        
Update DateNov 13, 2018 16:49

Chemical Taxonomy

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassNitrobenzenes
Intermediate Tree NodesNot available
Direct ParentNitrobenzenes
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsNitrobenzene - Nitroaromatic compound - Carboxamide group - C-nitro compound - Secondary alcohol - Secondary carboxylic acid amide - Organic nitro compound - Carboxylic acid derivative - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Alkyl chloride - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Aromatic alcohol - Organic zwitterion - Alkyl halide - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.

Properties

Property NameProperty Value
Molecular Weight323.126
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Complexity342
Monoisotopic Mass322.012
Exact Mass322.012
XLogP1.1
Formal Charge0
Heavy Atom Count20
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

References

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Antibiotic effects on seed germination and root development of tomato (Solanumlycopersicum L.).Ecotoxicol Environ Saf2018 Feb29035755
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Chloramphenicol stereoisomers need to be distinguished: consequences observedfrom a proficiency test.Food Addit Contam Part A Chem Anal Control Expo Risk Assess2017Apr28093042
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Exploration of deep eutectic solvent-based molecularly imprinted polymers assolid-phase extraction sorbents for screening chloramphenicol in milk.J Chromatogr Sci2017 Jul 128334778
Photoresponsive colorimetric immunoassay based on chitosan modified AgI/TiO2heterojunction for highly sensitive chloramphenicol detection.Biosens Bioelectron2017 Jan 1527619522
Novel single-stranded DNA binding protein-assisted fluorescence aptamer switchbased on FRET for homogeneous detection of antibiotics.Biosens Bioelectron2017 Jan 1527596250
Interfacing DNA Oligonucleotides with Calcium Phosphate and Other MetalPhosphates.Langmuir2017 Dec 2729228772
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Performance Assessment and Comparability of a Commercial Enzyme-LinkedImmunosorbent Assay Kit with Liquid Chromatography-Tandem Mass Spectrometry forChloramphenicol Residues in Crab and Shrimp.J Food Prot2016 Jan26735037
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A triple-amplification SPR electrochemiluminescence assay for chloramphenicolbased on polymer enzyme-linked nanotracers and exonuclease-assisted targetrecycling.Biosens Bioelectron2016 Dec 1527434234
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Selection and Identification of Chloramphenicol-Specific DNA Aptamers byMag-SELEX.Appl Biochem Biotechnol2016 Dec27613616
Engineered "hot" core-shell nanostructures for patterned detection ofchloramphenicol.Biosens Bioelectron2016 Apr 1526594888
A sensitive electrochemical aptasensor for multiplex antibiotics detection based on high-capacity magnetic hollow porous nanotracers coupling exonuclease-assistedcascade target recycling.Biosens Bioelectron2016 Apr 1526594886
Rapid surface enhanced Raman scattering detection method for chloramphenicolresidues.Spectrochim Acta A Mol Biomol Spectrosc2015 Jun 525754387