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Molecule
ID:69277
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₉N
Molecular Mass
143.18516
Exact Mass
143.07349929
Charge
0
InChI
InChI=1S/C10H9N/c1-8-6-9-4-2-3-5-10(9)7-11-8/h2-7H,1H3
InChIKey
FVVXWRGARUACNW-UHFFFAOYSA-N
Canonic Smiles
Cc1ncc2c(c1)cccc2
Isomeric Smiles
c1nc(cc2ccccc12)C
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
1.351692
LogD (pH = 7.4)
1.862614
Log P
1.8764203
Molar Refractivity
44.9428
Polarizability
18.836527
Polar Surface Area
12.89
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
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC name
•
Synonyms
•
IUPAC Traditional name
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
•
Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
074749
Sigma Aldrich
129895
Bide Pharmatech
BD40705
Academic Data
PubChem
14306
Names and Identifiers
IUPAC name
3-methylisoquinoline
Synonyms
3-Methylisoquinoline
3-甲基异喹啉
3-Methylisoquinoline
IUPAC Traditional name
isoquinolone-3-methyl
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Safety Statements
26
-
37/39
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
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
German water hazard class
3
Source
Risk Statements
36/37/38
Source
RTECS
NX2000000
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Signal Word
Warning
Source
Product Information
Purity
95+%
Source
98%
Source
Empirical Formula (Hill Notation)
C10H9N
Source
Physical Property
Melting Point
63-65 °C(lit.)
Source
Boiling Point
251 °C(lit.)
Source
Pharmacology Properties
Gene Information
human ... CYP1A2(1544)
Source
Molecule Details
Sigma Aldrich
129895
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
CAS Number
1125-80-0
PubChem SID
24847932
162035004
EC Number
214-412-5
MDL Number
MFCD00024139
PubChem CID
14306
Related Proteins
Related Proteins
Registration numbers
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CAS Number
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PubChem SID
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EC Number
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MDL Number
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PubChem CID
No Data Available
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