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Molecule
ID:37903
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₆ClNO₃
Molecular Mass
223.61254
Exact Mass
223.00362074
Charge
0
InChI
InChI=1S/C10H6ClNO3/c11-7-3-1-6(2-4-7)9-5-8(10(13)14)12-15-9/h1-5H,(H,13,14)
InChIKey
CRTZVRLESCICCT-UHFFFAOYSA-N
Canonic Smiles
Clc1ccc(cc1)c1onc(c1)C(=O)O
Isomeric Smiles
c1(noc(c1)c1ccc(cc1)Cl)C(=O)O
Calculated Properties
JChem
Acid pKa
3.905964
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
0.9525478
LogD (pH = 7.4)
-0.65800446
Log P
2.5524957
Molar Refractivity
54.2027
Polarizability
21.513481
Polar Surface Area
63.33
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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IUPAC name
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IUPAC Traditional name
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
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Physical Property
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F1984-0184
InterBioScreen
BB_SC-3634
Matrix Scientific
040715
Sigma Aldrich
644994
Enamine
EN300-26243
A&J Pharmtech
AJA-O30585
Academic Data
PubChem
1133644
Names and Identifiers
Synonyms
5-(4-Chlorophenyl)isoxazole-3-carboxylic acid
5-(4-Chlorophenyl)isoxazole-3-carboxylic acid
5-(4-氯苯基)异噁唑-3-羧酸
IUPAC name
5-(4-chlorophenyl)-1,2-oxazole-3-carboxylic acid
IUPAC Traditional name
5-(4-chlorophenyl)-1,2-oxazole-3-carboxylic acid
Registration numbers
MDL Number
MFCD06010034
CAS Number
33282-22-3
PubChem CID
1133644
PubChem SID
161001210
24883366
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Risk Statements
22
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H302
Source
European Hazard Symbols
Harmful (Xn)
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
German water hazard class
3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Product Information
Purity
95+%
Source
97%
Source
95%
Source
98%
Source
Empirical Formula (Hill Notation)
C10H6ClNO3
Source
Physical Property
Partition Coefficient
2.604
Source
Melting Point
200.0 °C (dec.)(lit.)
Source
185 - 187°C
Source
Hydrophobicity(logP)
3.162
Source
Molecule Details
Sigma Aldrich
644994
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay