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Merck
CN

276316

1-溴-3,5-二甲苯

97%

别名:

5-溴-m-二甲苯

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线性分子式:
(CH3)2C6H3Br
化学文摘社编号:
分子量:
185.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

1-溴-3,5-二甲苯, 97%

InChI

1S/C8H9Br/c1-6-3-7(2)5-8(9)4-6/h3-5H,1-2H3

SMILES string

Cc1cc(C)cc(Br)c1

InChI key

LMFRTSBQRLSJHC-UHFFFAOYSA-N

assay

97%

form

liquid

refractive index

n20/D 1.549 (lit.)

bp

202-204 °C (lit.)

density

1.362 g/mL at 25 °C (lit.)

functional group

bromo

Quality Level

Application

1-溴-3,5-二甲基苯已用于合成取代的2,2′-(二苯基磷烷基甲基)-1,1′-联萘衍生物

General description

钯催化的1-溴-3,5-二甲基苯和甲酚与氢氧化钾的碳氧偶联可生成甲苯基-3,5-二甲苯基醚

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

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Holger Klein et al.
Angewandte Chemie (International ed. in English), 40(18), 3408-3411 (2001-10-10)
Vittoria M Blasucci et al.
The journal of physical chemistry. A, 114(11), 3932-3938 (2010-03-20)
Tunable solvent systems couple homogeneous catalytic reactions to heterogeneous separations, thereby combining multiple unit operations into a single step and subsequently reducing waste generation and improving process economics. In addition, tunable solvents can require less energy than traditional separations, such
Tapan K Pal et al.
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By using a bent tetracarboxylic acid ligand that incorporates a pendent-NH2 functional group, a 3D Zn(II)-framework (1) based on Zn2 (CO2)4 secondary building units and Zn12 (CO2)24 supramolecular building blocks has been synthesized. Framework 1 is thermally less stable, which
Asami Yoshii et al.
Chemistry, an Asian journal, 15(14), 2181-2186 (2020-05-26)
Oligo-meta-phenylenes have been designed and synthesized as multipotent base materials of single-layer organic light-emitting devices. Simple molecular structures of oligo-meta-phenylenes composed of linear phenylene arrays benefited from the wealth of modern reactions available for biaryl couplings and were concisely synthesized

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