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Merck
CN

B71608

2-Bromomesitylene

98%

Synonym(s):

2-Bromo-1,3,5-trimethylbenzene

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About This Item

Linear Formula:
1,3,5-(CH3)3C6H2Br
CAS Number:
576-83-0
Molecular Weight:
199.09
Beilstein:
1907245
EC Number:
209-405-9
MDL number:
MFCD00000073
UNSPSC Code:
12352100
PubChem Substance ID:
24891976
NACRES:
NA.22

Key Documents

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Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.552 (lit.)

bp

225 °C (lit.)

mp

2 °C (lit.)

density

1.301 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(C)c(Br)c(C)c1

InChI

1S/C9H11Br/c1-6-4-7(2)9(10)8(3)5-6/h4-5H,1-3H3

InChI key

RRTLQRYOJOSPEA-UHFFFAOYSA-N

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General description

2-Bromomesitylene can be used as a reactant for carbon-carbon bond formation and cleavage reactions.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H335

Hazard Classifications

STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4275
STBL3541
STBK6317
STBJ6607
STBH4971

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Nitrile-group transfer from solvents to aryl halides. novel carbon- carbon bond formation and cleavage mediated by palladium and zinc species
Luo FH, et al.
Organometallics, 17, 1025-1030 (1998)
Karlee L Bamford et al.
Dalton transactions (Cambridge, England : 2003), 49(48), 17571-17577 (2020-11-25)
The synthesis and isolation of the first stable C-B-N-substituted borinium [MesBNiPr2][B(C6F5)4] (2) is described. Compound 2 was shown to react with isothiocyanate and carbodiimides, effecting B-C insertion to afford nitrilium (4) and borenium amidinate salts, respectively. The borinium cation [MesBNiPr2]+

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