544523
2′-Bromo-4′-methylacetanilide
98%
Synonym(s):
2-Bromo-4-methylacetanilide
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About This Item
Linear Formula:
CH3CONHC6H3(Br)CH3
CAS Number:
Molecular Weight:
228.09
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
assay
98%
mp
118-121 °C (lit.)
SMILES string
CC(=O)Nc1ccc(C)cc1Br
InChI
1S/C9H10BrNO/c1-6-3-4-9(8(10)5-6)11-7(2)12/h3-5H,1-2H3,(H,11,12)
InChI key
UUDGTWKIIUEVJD-UHFFFAOYSA-N
General description
2′-Bromo-4′-methylacetanilide(2-Bromo-4-methylacetanilide), an o-haloacetanilide derivative, can be prepared from 4-methylacetanilide via bromination.
Application
2′-Bromo-4′-methylacetanilide (2-Bromo-4-methylacetanilide) may be used in the preparation of 2,5-dimethyl-1H-1,3-benzazaphosphole and isomeric 1,2-disubstituted benzimidazoles.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Oxidative Bromination of Aromatic Amides using Sodium Perborate as Oxidant.
Hanson JR, et al.
J. Chem. Res. Synop., 11, 432-433 (1997)
Copper-catalyzed synthesis of benzimidazoles via cascade reactions of o-haloacetanilide derivatives with amidine hydrochlorides.
Yang D, et al.
The Journal of Organic Chemistry, 73(19), 7841-7844 (2008)
Ambident PCN Heterocycles: N?and P?Phosphanylation of Lithium 1,3?Benzazaphospholides.
Aluri BR, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 15(45), 12263-12272 (2009)