ChemicalBook > CAS DataBase List > 2-BROMO-N,N,4-TRIMETHYLANILINE

2-BROMO-N,N,4-TRIMETHYLANILINE

Product Name
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;Benzenamine, 2-bromo-N,N,4-trimethyl-
CBNumber
CB7110304
Molecular Formula
C9H12BrN
Formula Weight
214.1
MOL File
Mol file
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2-BROMO-N,N,4-TRIMETHYLANILINE Property

storage temp. 
Inert atmosphere,Room Temperature
Appearance
Colorless to light yellow Liquid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B613163
Product name
2-Bromo-N,N,4-trimethylaniline
Packaging
50mg
Price
$90
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0344007
Product name
2-BROMO-N,N,4-TRIMETHYLANILINE
Purity
95.00%
Packaging
1G
Price
$257.25
Updated
2021/12/16
AK Scientific
Product number
4354CU
Product name
2-Bromo-N,N,4-trimethylaniline
Packaging
5g
Price
$365
Updated
2021/12/16
Ambeed
Product number
A130093
Product name
2-Bromo-N,N,4-trimethylaniline
Purity
97%
Packaging
10g
Price
$453
Updated
2021/12/16
Crysdot
Product number
CD12093159
Product name
2-Bromo-N,N,4-trimethylaniline
Purity
97+%
Packaging
10g
Price
$505
Updated
2021/12/16
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2-BROMO-N,N,4-TRIMETHYLANILINE Chemical Properties,Usage,Production

Synthesis

99-97-8

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

2-BROMO-N,N,4-TRIMETHYLANILINE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-BROMO-N,N,4-TRIMETHYLANILINE Suppliers

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23667-06-3, 2-BROMO-N,N,4-TRIMETHYLANILINERelated Search:


  • 2-BROMO-N,N,4-TRIMETHYLANILINE
  • Benzenamine, 2-bromo-N,N,4-trimethyl-
  • 23667-06-3