2-(2-chlorophenoxy)-5-nitrobenzonitrile

Modify Date: 2025-09-21 07:29:52

2-(2-chlorophenoxy)-5-nitrobenzonitrile Structure
2-(2-chlorophenoxy)-5-nitrobenzonitrile structure
Common Name 2-(2-chlorophenoxy)-5-nitrobenzonitrile
CAS Number 99902-77-9 Molecular Weight 274.65900
Density 1.45g/cm3 Boiling Point 368.3ºC at 760 mmHg
Molecular Formula C13H7ClN2O3 Melting Point N/A
MSDS N/A Flash Point 176.5ºC

 Names

Name 2-(2-chlorophenoxy)-5-nitrobenzonitrile

 Chemical & Physical Properties

Density 1.45g/cm3
Boiling Point 368.3ºC at 760 mmHg
Molecular Formula C13H7ClN2O3
Molecular Weight 274.65900
Flash Point 176.5ºC
Exact Mass 274.01500
PSA 78.84000
LogP 4.43538
Index of Refraction 1.645
InChIKey OVUDUJKNHDOXEX-UHFFFAOYSA-N
SMILES N#Cc1cc([N+](=O)[O-])ccc1Oc1ccccc1Cl

 Precursor & DownStream

Precursor  2

DownStream  0

 2-(2-chlorophenoxy)-5-nitrobenzonitrileBioassay

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Name: Lowest concentration to reduce viral effect by 50% or more against Rhinovirus (RV)-2
Source: ChEMBL
Target: Enterovirus
External Id: CHEMBL799620
Name: Ratio of the MIC50 of 6-(4-Nitro-phenoxy)-nicotinonitrile compared to compound obtain...
Source: ChEMBL
Target: Enterovirus
External Id: CHEMBL800918
Name: Lowest concentration to reduce viral effect by 50% or more against Rhinovirus (RV)-1A
Source: ChEMBL
Target: Enterovirus
External Id: CHEMBL800917
Name: Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL4296184
Name: Ratio of the MIC50 of 6-(4-Nitro-phenoxy)-nicotinonitrile compared to compound obtain...
Source: ChEMBL
Target: Coxsackievirus
External Id: CHEMBL661536
Name: Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
Source: ChEMBL
Target: Klebsiella pneumoniae
External Id: CHEMBL4296186
Name: Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
Source: ChEMBL
Target: Escherichia coli
External Id: CHEMBL4296185
Name: Ratio of the MIC50 of 6-(4-Nitro-phenoxy)-nicotinonitrile compared to compound obtain...
Source: ChEMBL
Target: Enterovirus
External Id: CHEMBL799621
Name: Antiviral activity against Coxsackievirus B5 in african green monkey Vero cells
Source: ChEMBL
Target: Coxsackievirus B5
External Id: CHEMBL994937
Name: Antiviral activity against Coxsackievirus B4 in african green monkey Vero cells
Source: ChEMBL
Target: Coxsackievirus B4
External Id: CHEMBL994936
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