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About This Item
Linear Formula:
C10H7CH3
CAS Number:
Molecular Weight:
142.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-966-8
Beilstein/REAXYS Number:
506793
MDL number:
Assay:
95%
Form:
liquid
Quality Level
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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signalword
Danger
hcodes
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 Information
危险化学品
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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)
Pigments of marine animals. XII. The synthesis of certain substituted naphthopyrones related to crinoid pigments.
Rideout JA, et al.
Australian Journal of Chemistry, 29(5), 1087-1098 (1976)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M56808-100G | 04061834060239 |
| M56808-500G | 04061834060246 |
| M56808-5G | 04061834060253 |


