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Merck
CN

192376

4-溴-2,6-二甲基苯胺

98%

别名:

2,6-二甲基-4-溴苯胺

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关于此项目

线性分子式:
BrC6H2(CH3)2NH2
化学文摘社编号:
24596-19-8
分子量:
200.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851542
EC Number:
246-337-9
Beilstein/REAXYS Number:
1936300
MDL number:
MFCD00007826
Assay:
98%
Form:
solid

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产品名称

4-溴-2,6-二甲基苯胺, 98%

InChI key

QGLAYJCJLHNIGJ-UHFFFAOYSA-N

InChI

1S/C8H10BrN/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,10H2,1-2H3

SMILES string

Cc1cc(Br)cc(C)c1N

assay

98%

form

solid

mp

48-51 °C (lit.)

functional group

bromo

Quality Level

200

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相关类别

Application

4-Bromo-2,6-dimethylaniline has been used in the preparation of:
  • 4-bromo-N-(1-(6-(1-isopropyl-1H-benzo[d]imidazol-2-yl)pyridin-2-yl)ethylidene)-2,6-dimethylbenzenamine
  • N-(4-Bromo-2,6-dimethylphenyl)-5-trimethylammoniumsalicylaldimine chloride
  • ethynyl-functionalized persistent perylene diimide-multichromophore

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCX9845
BCCM9268
WXBF3933V
BCCH0528
BCCJ4260

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2-(1-Isopropyl-2-benzimidazolyl)-6-(1-aryliminoethyl) pyridyl transition metal (Fe, Co, and Ni) dichlorides: syntheses, characterizations and their catalytic behaviors toward ethylene reactivity.
Chen Y, et al.
Journal of Organometallic Chemistry, 693(10), 1829-1840 (2008)
Energy and electron transfer in ethynylene bridged perylene diimide multichromophores.
Flors C, et al.
The Journal of Physical Chemistry C, 111(12), 395-404 (2007)
Joseph B Binder et al.
Advanced synthesis & catalysis, 349(3), 395-404 (2007-02-02)
Tuning the electronic and steric environment of olefin metathesis catalysts with specialized ligands can adapt them to broader applications, including metathesis in aqueous solvents. Bidentate salicylaldimine ligands are known to stabilize ruthenium alkylidene complexes, as well as allow ring-closing metathesis

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