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Molecule
ID:41711
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆ClNO
Molecular Mass
167.59234
Exact Mass
167.0137915
Charge
0
InChI
InChI=1S/C8H6ClNO/c9-6-2-1-3-7-5(6)4-8(11)10-7/h1-3H,4H2,(H,10,11)
InChIKey
XNSPDJAXCBZCRV-UHFFFAOYSA-N
Canonic Smiles
O=C1Nc2c(C1)c(Cl)ccc2
Isomeric Smiles
N1C(=O)Cc2c1cccc2Cl
Calculated Properties
JChem
Acid pKa
11.4060335
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
1.6760943
LogD (pH = 7.4)
1.6760521
Log P
1.6760949
Molar Refractivity
44.3897
Polarizability
16.36837
Polar Surface Area
29.1
Rotatable Bonds
0
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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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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References
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Bioactivity
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General Information
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PubChem SID
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PubChem CID
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Safety Information
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
044887
Apollo Scientific
OR2754
Key Organics
5W-0090
Bide Pharmatech
BD28016
A&J Pharmtech
AJA-O4974
Academic Data
PubChem
1480686
Names and Identifiers
Synonyms
4-Chloro-1,3-dihydro-2H-indol-2-one
4-Chloro-2-oxindole
4-Chloro-1,3-dihydro-2H-indol-2-one
4-Chloroindolin-2-one
IUPAC name
4-chloro-2,3-dihydro-1H-indol-2-one
IUPAC Traditional name
4-chloro-1,3-dihydroindol-2-one
Registration numbers
MDL Number
MFCD03787567
CAS Number
20870-77-3
PubChem SID
162046474
PubChem CID
1480686
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
95+%
Source
>95%
Source
97%
Source
Physical Property
Melting Point
206-208°C
Source
206 - 208 °C
Source
Safety Information
MSDS Link
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Source
IRRITANT
Source
Irritant/Light Sensitive/Store under Argon/Keep Cold
Source
false
Source
Storage Warning
TSCA Listed