Basic information Safety Supplier Related

4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE

Basic information Safety Supplier Related

4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE Basic information

Product Name:
4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE
Synonyms:
  • 4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE
  • 4-broMo-2,6-bis(propan-2-yl)aniline
  • 4-BroMo-2,6-diisopropylaniline
  • Benzenamine,4-bromo-2,6-bis(1-methylethyl)-
  • 4-bromo-2,6-diisopropylbenzenamine
  • 4-Bromo-2,6-diisopropyl-phenylamine
  • 4-BROMO-2,6-BIS(1-METHYLETHYL)BENZEMINE
  • 2,6-diisopropyl-4-bromoaniline
CAS:
80058-84-0
MF:
C12H18BrN
MW:
256.18
EINECS:
202-303-5
Mol File:
80058-84-0.mol
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4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE Chemical Properties

Boiling point:
110 °C(Press: 0.14 Torr)
Density 
1.231±0.06 g/cm3(Predicted)
refractive index 
1.57
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Oil
pka
3.54±0.10(Predicted)
color 
Yellow to Brown
InChI
InChI=1S/C12H18BrN/c1-7(2)10-5-9(13)6-11(8(3)4)12(10)14/h5-8H,14H2,1-4H3
InChIKey
QAQRHTYPYQPBSX-UHFFFAOYSA-N
SMILES
C1(N)=C(C(C)C)C=C(Br)C=C1C(C)C
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Safety Information

HS Code 
2921.49.5000
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4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE Usage And Synthesis

Chemical Properties

White solid

Uses

4-Bromo-2,6-diisopropylaniline is used as a reactant in the preparation of hyperbranched ethylene oligomers.

Synthesis

24544-04-5

80058-84-0

To a stirred solution of 2,6-diisopropylaniline (14 g, 78.97 mmol, 1.00 eq.) in N,N-dimethylformamide (200 mL) was slowly added dropwise a solution of N-bromosuccinimide (NBS, 14 g, 78.65 mmol, 1.00 eq.) in N,N-dimethylformamide (100 mL) at 0 °C, the dropwise time was controlled to 60 min. The reaction mixture was continued to be stirred at 0 °C for 1 hour. Subsequently, water (900 mL) was added to the reaction system to quench the reaction. The reaction mixture was extracted with ethyl acetate (300 mL). The organic layers were combined and washed sequentially with saturated ammonium chloride solution (3 x 100 mL) and water (1 x 100 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 4-bromo-2,6-diisopropylaniline 20.05 g in 99% yield as a red oil.1H NMR (400 MHz, DMSO-d6): δ 6.95 (s, 2H), 4.77 (s, 2H), 5.47-5.39 (m, 1H), 3.04-2.98 (m, 1H) , 1.13 (d, J = 6.8 Hz, 12H) ppm.

References

[1] Patent: WO2012/116231, 2012, A2. Location in patent: Page/Page column 120
[2] Patent: US2014/323537, 2014, A1. Location in patent: Paragraph 0272
[3] Chemistry - A European Journal, 2015, vol. 21, # 44, p. 15676 - 15685
[4] Inorganic Chemistry, 2017, vol. 56, # 24, p. 14968 - 14978
[5] European Journal of Organic Chemistry, 2006, # 12, p. 2727 - 2738

4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINE Preparation Products And Raw materials

Raw materials

4-BROMO-2,6-BIS(1-METHYLETHYL)BENZENAMINESupplier

Shanghai Chenghe Medical Technology Co. Ltd. Gold
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021-021-54382182 18601603956
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18601603956@163.com
Ningbo Zeyu Chemical Technology Co., Ltd Gold
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15066123231
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2278736577@qq.com
Tianjin Zhongtian Xinchuang Technology Co., Ltd. Gold
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13312191509
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Energy Chemical
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021-021-58432009 400-005-6266
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sales8178@energy-chemical.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
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