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1-Bromo-2-methylnaphthalene / 100 G

Purity: 90 %
Synonym: 1-Bromo-2-methyl naphthalene; 1-bromo-2-methyl-naphthalene; 2-Methyl-1-bromonaphthalene
Molecular Formula: CH3C10H6Br
Molecular Weight: 221.09
SKU: MND-82727
CAS Number: 2586-62-1
MDL number: MFCD00003871
EC Number: 219-966-1
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100 G  
359.10 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P501
P305 + P351 + P338
P261
P271
P405
P302 + P352
P362 + P364
P403 + P233
P304 + P340
P321
P264 + P265
P319
P332 + P317
P337 + P317

Pictograms



Properties

Signal WordWarning
Flash Point (C)113 °C - closed cup
Flash Point (F)235.4 °F - closed cup
Density1.418 g/mL at 25 °C (lit.)
Boiling Point296 °C (lit.)

 Product Description

1-Bromo-2-methylnaphthalene is an organic compound featuring a naphthalene ring with a bromine atom and a methyl group attached. It is a pale yellow liquid used in organic synthesis.

 

Application

1-Bromo-2-methylnaphthalene is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It serves as a building block in various chemical reactions.

 

 

Articles:

- On the Dynamics of the Carbon–Bromine Bond Dissociation in the 1-Bromo-2-Methylnaphthalene Radical Anion

Publication Date: 15 July 2022

Marco Bonechi, Walter Giurlani, Massimo Innocenti, Dario Pasini, Suryakant Mishra, Roberto Giovanardi and Claudio Fontanesi

https://doi.org/10.3390/molecules27144539

 

- FT-IR, FT-Raman and UV spectral investigation: Computed frequency estimation analysis and electronic structure calculations on 1-bromo-2-methylnaphthalene

Publication Date: Available online 12 October 2012

M. Govindarajan a, M. Karabacak

https://doi.org/10.1016/j.saa.2012.09.099

 

- Synthesis and characterization of new chiral P,O ferrocenyl ligands and catalytic application to asymmetric Suzuki–Miyaura coupling

Publication Date: Available online 2 October 2014

Samer Bayda, Audrey Cassen, Jean-Claude Daran, Catherine Audin, Rinaldo Poli, Eric Manoury, Eric Deydier

https://doi.org/10.1016/j.jorganchem.2014.09.027