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192376

Sigma-Aldrich

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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About This Item

线性分子式:
BrC6H2(CH3)2NH2
CAS号:
24596-19-8
分子量:
200.08
Beilstein:
1936300
EC號碼:
246-337-9
MDL號碼:
MFCD00007826
分類程式碼代碼:
12352100
PubChem物質ID:
24851542
NACRES:
NA.22

品質等級

200

化驗

98%

形狀

solid

mp

48-51 °C (lit.)

官能基

bromo

SMILES 字串

Cc1cc(Br)cc(C)c1N

InChI

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

InChI 密鑰

QGLAYJCJLHNIGJ-UHFFFAOYSA-N

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相关类别

應用

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

訊號詞

Danger

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

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

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
BCCH0528
MKCQ6571
WXBD5425V
BCCF3435
BCCF3434

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乙二醛 溶液

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)
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)
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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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