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Molecule
ID:110718
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₀
Molecular Mass
142.1971
Exact Mass
142.07825032
Charge
0
InChI
InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3
InChIKey
QIMMUPPBPVKWKM-UHFFFAOYSA-N
Canonic Smiles
Cc1ccc2c(c1)cccc2
Isomeric Smiles
Cc1cc2ccccc2cc1
Calculated Properties
JChem
LogD (pH = 7.4)
3.48
LogD (pH = 5.5)
3.48
Log P
3.48
Rotatable Bonds
0
H Donor
0
H Acceptors
0
Lipinski's Rule of Five
true
Polar Surface Area
0.00
Polarizability
16.78
Molar Refractivity
47.55
LOG S
-3.78
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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General Information
Calculated Properties
•
RDKit
•
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
•
Synonyms
•
IUPAC name
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
•
Sigma Aldrich
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05216036
Sigma Aldrich
M57006
67890
45796
442359
Bide Pharmatech
BD77300
Alfa Aesar
L02459
A&J Pharmtech
AJA-O11917
Academic Data
PubChem
7055
ChEBI
CHEBI:50720
Names and Identifiers
IUPAC Traditional name
2-methylnaphthalene
Synonyms
2-METHYLNAPHTHALENE
2-Methylnaphthalene (β)
2-甲基萘 (β)
β-甲基萘
2-甲基萘
β-Methylnaphthalene
2-Methylnaphthalene
beta-Methylnaphthalene
2-methylnaphthalene
2-Methylnaphthalene
IUPAC name
2-methylnaphthalene
Registration numbers
CAS Number
91-57-6
EC Number
202-078-3
PubChem CID
7055
PubChem SID
162096492
24884864
24897037
24867811
24869412
56352859
Beilstein Number
906859
MDL Number
MFCD00004118
PubMed Citation Links
24440761
22324881
24117136
21478643
22002322
SureChEMBL Database
SCHEMBL36453
Patent number
EP1188733
UM-BBD compID
c0699
CHEMBL
CHEMBL195895
BRENDA Database
1.14.12.12
1.11.2.1
CHEBI ID
CHEBI:50720
CHEBI:19705
CHEBI:34296
ACToR Database
91-57-6
7419-61-6
CompTox Database
DTXSID4020878
BindingDB Database
50159241
BRENDA Ligand Database
84149
KEGG ID
C14098
NMRShiftDB Database
10008957
BKMS React Database
84149
Reaxys Registry
906859
Molecule Details
MP Biomedicals
05216036
MP Biomedicals Rare Chemical collection
Sigma Aldrich
M57006
Packaging
100, 500 g in glass bottle
ChEBI
CHEBI:50720
A methylnaphthalene carrying a methyl substituent at position 2.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
EC Number
•
PubChem CID
•
PubChem SID
•
Beilstein Number
•
MDL Number
•
PubMed Citation Links
•
SureChEMBL Database
•
Patent number
•
UM-BBD compID
•
CHEMBL
•
BRENDA Database
•
CHEBI ID
•
ACToR Database
•
CompTox Database
•
BindingDB Database
•
BRENDA Ligand Database
•
KEGG ID
•
NMRShiftDB Database
•
BKMS React Database
•
Reaxys Registry
Properties
•
Physical Property
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Product Information
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Safety Information
•
Pharmacology Properties
Properties
Physical Property
Density
1.0058 g/ml
Source
1 g/mL at 25 °C(lit.)
Source
1.001
Source
Boiling Point
241°C
Source
241-242 °C(lit.)
Source
241-243°C
Source
Melting Point
34.6°C
Source
34-36 °C(lit.)
Source
31-35°C
Source
208.4 °F
Source
98 °C
Source
97°C(206°F)
Source
Product Information
Download link
Source
C10H7CH3
Source
97%
Source
≥95.0% (GC)
Source
98%
Source
~2% 1-methylnaphthalene
Source
Safety Information
Harmful (Xn)
Pharmacology Properties
human ... CYP1A2(1544), CYP2A6(1548)mouse ... Cyp2a5(13087)
Source
human ... CYP1A2(1544)
Source
Empirical Formula (Hill Notation)
C11H10
Source
Grade
purum
Source
analytical standard, for environmental analysis
Source
analytical standard
Source
Packaging
ampule of 1000 mg
Source
Source
Nature polluting (N)
Source
Harmful (X)
Source
Risk Statements
R:
22
Source
22
-
36/37/38
-
51/53
Source
22
-
36/38
-
51/53
Source
Safety Statements
S:
36/37/39
Source
26
-
37/39
-
61
Source
26
-
36/37
-
61
Source
RTECS
QJ9635000
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
RID/ADR
UN 3077 9/PG 3
Source
Hazard Class
9
Source
Packing Group
3
Source
III
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H302
-
H315
-
H319
-
H335
-
H411
Source
H301
-
H315
-
H319
-
H411
-
H401
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
UN Number
3077
Source
UN3077
Source
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
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
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
German water hazard class
2
Source
GHS Precautionary statements
P261
-
P273
-
P305+P351+P338
Source
P280
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
TSCA Listed
是
Source
Flash Point
Certificate of Analysis
Linear Formula
Purity
Impurities
European Hazard Symbols
Gene Information
Source
Source