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Molecule
ID:70418
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/c1-8-10-5-3-2-4-9(10)6-7-11-8/h2-7H,1H3
InChIKey
PBYMYAJONQZORL-UHFFFAOYSA-N
Canonic Smiles
Cc1nccc2c1cccc2
Isomeric Smiles
c1(nccc2ccccc12)C
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
1.2843906
LogD (pH = 7.4)
1.8589985
Log P
1.8764203
Molar Refractivity
44.9428
Polarizability
18.836992
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
No Data Available
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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
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
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Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
075958
Apollo Scientific
OR24943
Sigma Aldrich
264938
Alfa Aesar
H27029
Bide Pharmatech
BD0451
A&J Pharmtech
AJA-O1076
Academic Data
PubChem
15592
Names and Identifiers
IUPAC Traditional name
isoquinoline, 1-methyl-
IUPAC name
1-methylisoquinoline
Synonyms
1-Methylisoquinoline
1-甲基异喹啉
1-Methylisoquinoline
1-甲基异喹啉基
Registration numbers
CAS Number
1721-93-3
EC Number
217-017-6
MDL Number
MFCD00006902
PubChem SID
162036137
24856043
PubChem CID
15592
Molecule Details
Sigma Aldrich
264938
Caution
Low melting solid
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
EC Number
•
MDL Number
•
PubChem SID
•
PubChem CID
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Warning
Source
26
-
36
Source
26
-
37
Source
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
H315
-
H319
-
H335
Source
Irritant (Xi)
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
36/37/38
Source
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
3
Source
Product Information
95+%
Source
97%
Source
98%
Source
C10H9N
Source
Physical Property
235.4 °F
Source
113 °C
Source
>110°C(230°F)
Source
126-128 °C/16 mmHg(lit.)
Source
126-128°C/16mm
Source
1.078 g/mL at 25 °C(lit.)
Source
1.078
Pharmacology Properties
human ... CYP2A6(1548)mouse ... Cyp2a5(13087)
Source
Source
Source
Source
n20/D 1.6140(lit.)
Source
1.6140
Source
10-12°C
Source
GHS Signal Word
Safety Statements
GHS Pictograms
GHS Hazard statements
European Hazard Symbols
GHS Precautionary statements
Risk Statements
Personal Protective Equipment
German water hazard class
Purity
Empirical Formula (Hill Notation)
Flash Point
Boiling Point
Density
Gene Information
Refractive Index
Melting Point