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2-Bromo-n,n,4-trimethylaniline

CAS No.
23667-06-3
Chemical Name:
2-Bromo-n,n,4-trimethylaniline
Synonyms
2-Bromo-n,n,4-trimethylaniline;2-bromo-N,N,4-trimethylbenzeneamine;Benzenamine, 2-bromo-N,N,4-trimethyl-
CBNumber:
CB7110304
Molecular Formula:
C9H12BrN
Molecular Weight:
214.1
MDL Number:
MFCD07780654
MOL File:
Mol file
MSDS File:
SDS
Last updated:2026-09-12 18:54:27

2-Bromo-n,n,4-trimethylaniline Properties

storage temp. Inert atmosphere,Room Temperature
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338

2-Bromo-n,n,4-trimethylaniline price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS47871 2-Bromo-N,N,4-trimethylaniline 97% 23667-06-3 1g $84 2026-06-04 Buy
Activate Scientific AS47871 2-Bromo-N,N,4-trimethylaniline 97% 23667-06-3 5g $291 2026-06-04 Buy
aablocks AA002NZF 2-Bromo-N,N,4-trimethylaniline 98% 23667-06-3 1g $25 2026-05-28 Buy
aablocks AA002NZF 2-Bromo-N,N,4-trimethylaniline 98% 23667-06-3 5g $115 2026-05-28 Buy
aablocks AA002NZF 2-Bromo-N,N,4-trimethylaniline 98% 23667-06-3 10g $218 2026-05-28 Buy
Product number Packaging Price Buy
AS47871 1g $84 Buy
AS47871 5g $291 Buy
AA002NZF 1g $25 Buy
AA002NZF 5g $115 Buy
AA002NZF 10g $218 Buy

2-Bromo-n,n,4-trimethylaniline Chemical Properties,Uses,Production

Synthesis

N,N-Dimethyl-p-toluidine

99-97-8

2-BROMO-N,N,4-TRIMETHYLANILINE

23667-06-3

General procedure for the synthesis of 2-bromo-N,N,4-trimethylaniline from N,N-dimethyl-p-toluidine: In a round-bottomed flask, N,N-dimethyl-p-toluidine (1 mmol) was mixed with 48% aqueous hydrobromic acid (1 mL) in dimethyl sulfoxide (DMSO, 1 mL). The reaction mixture was stirred at the indicated temperature for 1-4 hours. After completion of the reaction, it was cooled to room temperature and the pH of the reaction solution was adjusted to 7-8 with 4 M aqueous sodium hydroxide.Subsequently, the reaction mixture was extracted twice with ethyl acetate (EtOAc) and the organic phases were combined. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product 2-bromo-N,N,4-trimethylaniline.

References

[1] Journal of Chemical Research, 2014, vol. 38, # 10, p. 593 - 596
[2] Synthesis, 2009, # 21, p. 3672 - 3676
[3] Synthetic Communications, 2010, vol. 40, # 19, p. 2954 - 2962
[4] Tetrahedron Letters, 2007, vol. 48, # 45, p. 7969 - 7973
[5] Chemische Berichte, 1908, vol. 41, p. 2117

99-97-8
23667-06-3
Synthesis of 2-Bromo-n,n,4-trimethylaniline from N,N-Dimethyl-p-toluidine

2-Bromo-n,n,4-trimethylaniline Preparation Products And Raw materials

Raw materials

Preparation Products

2-Bromo-n,n,4-trimethylaniline Suppliers

Global( 31)Suppliers
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Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
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Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Aikon International Limited 025-58859352 13913916777 dt3@aikonchem.com China 15490 58
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2-Bromo-n,n,4-trimethylaniline Spectrum

Benzenamine, 2-bromo-N,N,4-trimethyl- 2-bromo-N,N,4-trimethylbenzeneamine 2-Bromo-n,n,4-trimethylaniline 23667-06-3