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2-(brommethyl)naphthalen

Names

[ CAS No. ]:
939-26-4

[ Name ]:
2-(brommethyl)naphthalen

[Synonym ]:
2-(bromomethyl)napthalene
2-(brommethyl)naphthalen
β-(Bromomethyl)naphthalene
2-Bromomethyl naphthalene
2-naphthylmethyl bromide
Naphthalene, 2-(bromomethyl)-
Naphthalene,2-(bromomethyl)
2-Bromomethylnaphthalene
EINECS 213-359-5
MFCD00004123
2-(Bromomethyl)naphthalene

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
293.3±0.0 °C at 760 mmHg

[ Melting Point ]:
51-54 °C(lit.)

[ Molecular Formula ]:
C11H9Br

[ Molecular Weight ]:
221.093

[ Flash Point ]:
151.8±12.3 °C

[ Exact Mass ]:
219.988754

[ LogP ]:
4.15

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.664

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H317

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C:Corrosive

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S28-S36/37/39-S45-S37

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
29033036

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 29033036

Articles

Enzymatic surface modification and functionalization of PET: a water contact angle, FTIR, and fluorescence spectroscopy study.

Biotechnol. Bioeng. 103(5) , 845-56, (2009)

The purpose of this study was to investigate the changes induced by a lypolytic enzyme on the surface properties of polyethylene terephthalate (PET). Changes in surface hydrophilicity were monitored b...

Preparation and isolation of dithiolene thiophosphoryl molecules as stable, protected forms of dithiolene ligands.

Inorg. Chem. 46(8) , 3283-8, (2007)

The reaction of P4S10 with acyloins, RC(O)CH(OH)R, in refluxing dioxane, followed by the addition of alkylating agents, forms dithiolene thiophosphoryl thiolate compounds, (R2C2S2)P(S)(SR'), which are...


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Related Compounds