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Molecule
ID:41938
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₅ClN₂O₃
Molecular Mass
212.5899
Exact Mass
211.99886971
Charge
0
InChI
InChI=1S/C8H5ClN2O3/c9-4-8-10-6-3-5(11(12)13)1-2-7(6)14-8/h1-3H,4H2
InChIKey
AQZQGQKSWZXRCF-UHFFFAOYSA-N
Canonic Smiles
ClCc1oc2c(n1)cc(cc2)[N+](=O)[O-]
Isomeric Smiles
c1(ccc2c(c1)nc(o2)CCl)[N+](=O)[O-]
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
1.9202582
LogD (pH = 7.4)
1.9202582
Log P
1.9202582
Molar Refractivity
48.2375
Polarizability
19.4421
Polar Surface Area
69.17
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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IUPAC name
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PubChem SID
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Molecular Spectra
Molecule Details
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
045145
Key Organics
6X-0702
Enamine
EN300-102161
A&J Pharmtech
AJA-O35146
Academic Data
PubChem
2764189
Names and Identifiers
Synonyms
2-(Chloromethyl)-5-nitro-1,3-benzoxazole
IUPAC name
2-(chloromethyl)-5-nitro-1,3-benzoxazole
IUPAC Traditional name
2-(chloromethyl)-5-nitro-1,3-benzoxazole
Registration numbers
MDL Number
MFCD01596292
PubChem SID
162046701
PubChem CID
2764189
CAS Number
119198-10-6
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
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Physical Property
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Product Information
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Safety Information
Properties
Physical Property
Melting Point
115-117°C
Source
115 - 117 °C
Source
115 - 117°C
Source
Hydrophobicity(logP)
1.855
Source
Product Information
Purity
>95%
Source
95%
Source
98%
Source
Safety Information
IRRITANT
Source
Download link
Source
false
Source
Storage Warning
MSDS Link
TSCA Listed