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M56808

1-Methylnaphthalene

95%

Synonym(s):

1-MN

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About This Item

Linear Formula:
C10H7CH3
CAS Number:
90-12-0
Molecular Weight:
142.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897036
EC Number:
201-966-8
Beilstein/REAXYS Number:
506793
MDL number:
MFCD00004034
Assay:
95%
Form:
liquid
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Quality Level

100

assay

95%

form

liquid

autoignition temp.

984 °F

refractive index

n20/D 1.615 (lit.)

bp

240-243 °C (lit.)

mp

−22 °C (lit.)

density

1.001 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc2ccccc12

InChI

1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3

InChI key

QPUYECUOLPXSFR-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

Application

1-Methylnaphthalene can be used in:
  • The synthesis of various polycyclic aromatic hydrocarbons (PAHs), including naphtho[a]carbazoles and naphthopyrones.
  • The preparation of 1-methylnaphthalene based tocainide analog as skeletal muscle voltage-gated sodium channel blocker.
  • The synthesis of aminobenzoyl-2-hydroxy-1-naphthyl hydrazine, a potential HIV reverse-transcriptase-DNA-polymerase inhibitor (RTI).

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

Group 4: Flammable liquids + Type 3 petroleums + Hazardous rank III + Water insoluble liquid

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

M56808-500G:4.548173991177E12 + M56808-5G:4.548173991184E12 + M56808-100G:4.54817399116E12

jan

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Certificates of Analysis (COA)

Lot/Batch Number
76196TJ
S52646
04426CJ
S47091
S43316

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A versatile synthesis of annulated carbazole analogs involving a domino reaction of bromomethylindoles with arenes/heteroarenes.
Dhayalan V, et al.
European Journal of Organic Chemistry, 2009(4), 531-546 (2009)
From 1-Methylnaphthalene to Aminobenzoyl-2-Hydroxy-1-naphthyl hydrazone.
Genov K and Nikolova D
Journal of the University of Chemical Technology and Metallurgy, 44(3), 281-285 (2009)
N-Aryl-2, 6-dimethylbenzamides, a new generation of tocainide analogues as blockers of skeletal muscle voltage-gated sodium channels.
Muraglia M, et al.
Journal of Medicinal Chemistry, 57(6), 2589-2600 (2014)
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