M57006
2-Methylnaphthalene (β)
95%
Synonym(s):
β-Methylnaphthalene
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About This Item
Linear Formula:
C10H7CH3
CAS Number:
Molecular Weight:
142.20
Beilstein:
906859
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
95%
bp
241-242 °C (lit.)
mp
34-36 °C (lit.)
density
1 g/mL at 25 °C (lit.)
SMILES string
Cc1ccc2ccccc2c1
InChI
1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3
InChI key
QIMMUPPBPVKWKM-UHFFFAOYSA-N
Gene Information
human ... CYP1A2(1544) , CYP2A6(1548)
mouse ... Cyp2a5(13087)
Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
208.4 °F - closed cup
Flash Point(C)
98.0 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Florin Musat et al.
Environmental microbiology, 11(1), 209-219 (2008-09-25)
The anaerobic biodegradation of naphthalene, an aromatic hydrocarbon in tar and petroleum, has been repeatedly observed in environments but scarcely in pure cultures. To further explore the relationships and physiology of anaerobic naphthalene-degrading microorganisms, sulfate-reducing bacteria (SRB) were enriched from
P B Nagabalasubramanian et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 43-52 (2011-10-26)
In this work, the FT-IR and FT-Raman spectrum of 1-(chloromethyl)-2-methyl naphthalene (abbreviated as 1-ClM-2MN, C(12)H(11)Cl) have been recorded in the region 3600-10cm(-1). The optimum molecular geometry, normal mode wavenumbers, infrared and Raman intensities, Raman scattering activities, corresponding vibrational assignments, Mullikan
Kazutoshi Shindo et al.
Bioscience, biotechnology, and biochemistry, 75(3), 505-510 (2011-03-11)
We performed combinational bioconversion of substituted naphthalenes with PhnA1A2A3A4 (an aromatic dihydroxylating dioxygenase from marine bacterium Cycloclasticus sp. strain A5) and prenyltransferase NphB (geranyltransferase from Streptomyces sp. strain CL190) or SCO7190 (dimethylallyltransferase from Streptomyces coelicolor A3(2)) to produce prenyl naphthalen-ols.
Yu Wang et al.
Chemical communications (Cambridge, England), (8)(8), 1090-1091 (2005-02-19)
Using sodium deoxycholate as a protective medium, the selective recognition of Cu(II) at ng ml(-1) level is realized through dynamic phosphorescence quenching of 1-bromo-2-methylnaphthalene (BMN) without deoxygenation. The limit of detection is 4.32 ng ml(-1), and the relative standard deviation
Drazenka Selesi et al.
Journal of bacteriology, 192(1), 295-306 (2009-10-27)
The highly enriched deltaproteobacterial culture N47 anaerobically oxidizes the polycyclic aromatic hydrocarbons naphthalene and 2-methylnaphthalene, with sulfate as the electron acceptor. Combined genome sequencing and liquid chromatography-tandem mass spectrometry-based shotgun proteome analyses were performed to identify genes and proteins involved
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