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Molecule
ID:89935
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/c9-6-3-1-2-5-4-7(11)10-8(5)6/h1-3H,4H2,(H,10,11)
InChIKey
FPDLUAACCNVSQA-UHFFFAOYSA-N
Canonic Smiles
O=C1Cc2c(N1)c(Cl)ccc2
Isomeric Smiles
N1C(=O)Cc2c1c(ccc2)Cl
Calculated Properties
JChem
Acid pKa
11.635436
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
1.6760945
LogD (pH = 7.4)
1.6760699
Log P
1.6760949
Molar Refractivity
44.3897
Polarizability
16.377008
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
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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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RDKit
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Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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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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Safety Information
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Physical Property
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Product Information
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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
Apollo Scientific
OR5622
Sigma Aldrich
691712
Bide Pharmatech
BD20202
A&J Pharmtech
AJA-O4148
AJA-O31425
Academic Data
PubChem
3731010
Names and Identifiers
IUPAC name
7-chloro-2,3-dihydro-1H-indol-2-one
Synonyms
7-Chloroindolin-2-one
7-Chloro-1,3-dihydro-2H-indol-2-one
7-Chloro-2-oxindole 97%
7-Chloro-2-oxindole
7-氯氧化吲哚
IUPAC Traditional name
7-chloro-1,3-dihydroindol-2-one
Registration numbers
MDL Number
MFCD06656001
CAS Number
25369-33-9
129295-32-5
PubChem CID
3731010
PubChem SID
162076790
Properties
Safety Information
Storage Warning
Irritant
Source
Safety Statements
61
Source
GHS Precautionary statements
P305+P351+P338
Source
German water hazard class
3
Source
GHS Hazard statements
H302
-
H319
Source
European Hazard Symbols
Harmful (Xn)
Source
MSDS Link
Download link
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
22
-
52/53
Source
GHS Signal Word
Warning
Source
Physical Property
Melting Point
218-222°C
Source
221-225 °C
Source
Product Information
Empirical Formula (Hill Notation)
C8H6ClNO
Source
Purity
97%
Source
95+%
Source
98%
Source
Molecule Details
Sigma Aldrich
691712
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay