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Merck
CN

116157

1,4-二溴-2,5-二甲基苯

98%

别名:

2,5-二溴-对二甲苯

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线性分子式:
(CH3)2C6H2Br2
化学文摘社编号:
分子量:
263.96
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-038-2
MDL number:
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产品名称

1,4-二溴-2,5-二甲基苯, 98%

InChI key

QENIALCDPFDFHX-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1cc(Br)c(C)cc1Br

assay

98%

form

solid

bp

261 °C (lit.)

mp

72-74 °C (lit.)

functional group

bromo

Quality Level

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Application

1,4-二溴-2,5-二甲苯已被用于制备4,4″-二甲酰基-2′,5′-二甲基-1,1′.4′,1″-三联苯。它也被用于制备1,4-二甲酰基-2,5-二甲基苯

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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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
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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