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116157

Sigma-Aldrich

1,4-Dibromo-2,5-dimethylbenzene

98%

Synonym(s):

2,5-Dibromo-p-xylene

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25 G
$68.00
100 G
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About This Item

Linear Formula:
(CH3)2C6H2Br2
CAS Number:
1074-24-4
Molecular Weight:
263.96
EC Number:
214-038-2
MDL number:
MFCD00000091
UNSPSC Code:
12352100
PubChem Substance ID:
24847267
NACRES:
NA.22

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Quality Level

100

assay

98%

form

solid

bp

261 °C (lit.)

mp

72-74 °C (lit.)

functional group

bromo

SMILES string

Cc1cc(Br)c(C)cc1Br

InChI

1S/C8H8Br2/c1-5-3-8(10)6(2)4-7(5)9/h3-4H,1-2H3

InChI key

QENIALCDPFDFHX-UHFFFAOYSA-N

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Application

1,4-dibromo-2,5-dimethylbenzene has been used in the preparation of 4,4″-diformyl-2′,5′-dimethyl-1,1′.4′,1″-terphenyl[1]. It has also been used in the preparation of 1,4-diformyl-2,5-dimethylbenzene[2].

pictograms

Exclamation markEnvironment
GHS07,GHS09

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Warning

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW3389
MKCR7515
MKCM7637
MKCL5002
MKCK7475

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Nikolai Kuhnert et al.
Organic & biomolecular chemistry, 1(7), 1157-1170 (2003-08-21)
The synthesis of aromatic dicarboxaldehydes, using dilithiation methodology is described along with their reactivity, in the [3 + 3] cyclocondensation reaction, with (1R,2R)-diaminocyclohexane to give trianglimine macrocycles. The scope and limitations of the cyclocondensation reaction are studied and some comments
Yuxiang Du et al.
Light, science & applications, 9, 151-151 (2020-09-10)
Tuneable microlasers that span the full visible spectrum, particularly red, green, and blue (RGB) colors, are of crucial importance for various optical devices. However, RGB microlasers usually operate in multimode because the mode selection strategy cannot be applied to the
Nikolai Kuhnert et al.
Organic & biomolecular chemistry, 3(10), 1911-1921 (2005-05-13)
The synthesis of aromatic dicarboxaldehydes is described along with their reactivity in the [3 + 3] cyclocondensation reaction with (1R,2R)-diaminocyclohexane to give trianglimine macrocycles. In particular, the scope and limitation of the reaction with regard to complete control of the

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