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143677

Sigma-Aldrich

2-(Bromomethyl)naphthalene

96%

Synonym(s):

β-(Bromomethyl)naphthalene, β-Naphthylmethyl bromide, (Naphthalen-2-yl)methyl bromide, 2-(Bromomethyl)naphthalene, 2-Menaphthyl bromide, 2-Naphthylmethyl bromide

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About This Item

Linear Formula:
C10H7CH2Br
CAS Number:
Molecular Weight:
221.09
Beilstein:
636546
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

bp

213 °C/100 mmHg (lit.)

mp

51-54 °C (lit.)

storage temp.

2-8°C

SMILES string

BrCc1ccc2ccccc2c1

InChI

1S/C11H9Br/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2

InChI key

RUHJZSZTSCSTCC-UHFFFAOYSA-N

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Application

2-(Bromomethyl)naphthalene (2-BMN) can be employed as a starting material in the synthesis of 2-(fluoromethyl)naphthalene , 2-naphthylmethyl azide , 2-naphthalenecarboxaldehyde , diselenide, bis(2-naphthalenylmethyl) , 1H-1,2,3-triazole, 4,4′-(1,4-phenylene)bis[1-(2-naphthalenylmethyl).

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Probing the reactivity of o-phthalaldehydic acid/methyl ester: synthesis of N-isoindolinones and 3-arylaminophthalides
Mamidyala SK and Cooper MA
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ACS sustainable chemistry & engineering, 4(3), 1123-1130 (2016)
A novel and efficient method for the synthesis of dibenzyl diselenides
Tian F and Lu S
J. Chem. Res. (M), 2004(9), 632-633 (2004)
Kuppuswamy Arumugam et al.
Inorganic chemistry, 46(8), 3283-3288 (2007-03-16)
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 readily isolated and purified. The compounds that have been prepared and identified spectroscopically are those

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