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Molecule
ID:67113
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₇NO
Molecular Mass
145.15798
Exact Mass
145.05276385
Charge
0
InChI
InChI=1S/C9H7NO/c11-9-3-1-2-7-6-10-5-4-8(7)9/h1-6,11H
InChIKey
CSNXUYRHPXGSJD-UHFFFAOYSA-N
Canonic Smiles
Oc1cccc2c1ccnc2
Isomeric Smiles
c1nccc2c(cccc12)O
Calculated Properties
JChem
Acid pKa
9.450011
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
1.3929899
LogD (pH = 7.4)
1.4369944
Log P
1.4414848
Molar Refractivity
42.3322
Polarizability
17.59222
Polar Surface Area
33.12
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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RDKit
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Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
072532
Apollo Scientific
OR2817
ChemBridge
4034700
InterBioScreen
BB_SC-2702
Sigma Aldrich
H33207
TRC
H953260
Alfa Aesar
B25052
Bide Pharmatech
BD11579
A&J Pharmtech
AJA-O4280
Academic Data
PubChem
30386
Names and Identifiers
Synonyms
5-Hydroxyisoquinoline
5-isoquinolinol
Isoquinolin-5-ol
5-Hydroxy-2-azanaphthalene
5-Hydroxyisoquinoline 90%
isoquinolin-5-ol
5-Isoquinolinol
5-异喹啉醇
5-Hydroxyisoquinoline
5-羟基异喹啉
NSC 51787
IUPAC Traditional name
isoquinolin-5-ol
IUPAC name
isoquinolin-5-ol
Registration numbers
MDL Number
MFCD00006906
CAS Number
2439-04-5
EC Number
219-456-9
PubChem SID
24895571
162032849
PubChem CID
30386
Molecule Details
Sigma Aldrich
H33207
Packaging
25 g in poly bottle
5 g in glass bottle
TRC
H953260
Reagent used in the preparation of PARP inhibitor.
References
PubChem Literature
From Data Sources
•
Tran, T., et al.: Bioorg. Med. Chem. Lett., 19, 5250 (2009)
•
Bodendiek, S., et al.: Eur. J. Med. Chem., 44, 1838 (2009)
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
EC Number
•
PubChem SID
•
PubChem CID
Properties
Product Information
Purity
95+%
Source
90%
Source
tech. 90%
Source
95%
Source
Empirical Formula (Hill Notation)
C9H7NO
Source
Grade
technical grade
Source
Certificate of Analysis
Download link
Source
Safety Information
Download link
Source
Download link
Source
Download link
Source
false
Source
否
Source
Physical Property
213-215°C
Source
Brown Solid
Source
Storage Warning
IRRITANT
Source
Harmful/Irritant/Hygroscopic/Store under Argon
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
37/39
Source
26
-
37
Source
GHS Signal Word
Warning
Source
Risk Statements
36/37/38
Source
German water hazard class
3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
European Hazard Symbols
Irritant (Xi)
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
MSDS Link
TSCA Listed
Melting Point
Apperance