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192376

Sigma-Aldrich

4-Bromo-2,6-dimethylaniline

98%

Synonym(s):

4-Bromo-2,6-xylidine

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About This Item

Linear Formula:
BrC6H2(CH3)2NH2
CAS Number:
24596-19-8
Molecular Weight:
200.08
Beilstein:
1936300
EC Number:
246-337-9
MDL number:
MFCD00007826
UNSPSC Code:
12352100
PubChem Substance ID:
24851542
NACRES:
NA.22

Quality Level

200

Assay

98%

form

solid

mp

48-51 °C (lit.)

functional group

bromo

SMILES string

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 key

QGLAYJCJLHNIGJ-UHFFFAOYSA-N

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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

Signal Word

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

Q192376-VAR:
Q192376-BULK:
192376-BULK:
192376-100G:
192376-VAR:
192376-25G:
192376-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH0528
MKCQ6571
WXBD5425V
BCCF3435
BCCF3434

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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.
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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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