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590517

Sigma-Aldrich

2-Bromo-N,N-dimethylaniline

97%

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Empirical Formula (Hill Notation):
C8H10BrN
CAS Number:
Molecular Weight:
200.08
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

SMILES string

CN(C)c1ccccc1Br

InChI

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

InChI key

ONMSBNJJCUCYED-UHFFFAOYSA-N

Application

2-Bromo-N,N-dimethylaniline may be used in the synthesis of the following:
  • bis[(2-dimethylamino)phenyl]amine via a multi-step reaction procedure
  • 2-(N,N-dimethylaminophenyl)-bis(diethylamino)phosphine
  • 6-[2-(dimethylamino)phenyl]-2,2-bipyridine obtained via lithiation followed by reaction with 2,2-bipyridine
  • 1-(2′-(dimethylamino)phenyl)-2-diphenylphosphino-3-methylimidazolium trifluoromethanesulfonate via a multi-step reaction procedure

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - STOT RE 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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?Synthesis, Structures, and Luminescent Properties of d10 Group 12 Metal Complexes with Substituted 2,2-Bipyridine Ligands?
Liu m-x, et al.
European Journal of Inorganic Chemistry, 2006(21), 4317-4323 (2006)
?Rhodium complexes with a new chiral nitrogencontaining
Binol-based diphosphite or phosphonite ligand: synthesis and application to hydroformylation of styrene and/or hydrogenation of prochiral olefins?
Kostas.D I
Applied Organometallic Chemistry, 19(10), 1090-1095 (2005)
?Synthesis, Structures, and Luminescent Properties of d10 Group 12 Metal Complexes with Substituted 2,2-Bipyridine Ligands?
Chen J-S, et al.
J. Mol. Catal. A: Chem., 396, 68-76 (2015)
?Pd, Pt, and Ru complexes of a pincer bis(amino)amide ligand?
Ren P, et al.
Dalton Transactions, 40(35), 8906-8911 (2011)

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