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(2-BROMOBENZYL)METHYLAMINE

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(2-BROMOBENZYL)METHYLAMINE Basic information

Product Name:
(2-BROMOBENZYL)METHYLAMINE
Synonyms:
  • (2-BROMOBENZYL)METHYLAMINE
  • 2-BROMO-N-METHYLBENZYLAMINE
  • (2-Bromobenzyl)methylamine95%
  • N-Methyl-2-bromobenzylamine
  • 2-Bromo-N-methyl-Benzenemethanamine
  • (2-BROMOBENZYL)METHY
  • 2-(2-broMophenyl)ethan-1-aMine
  • 2-Bromo-N-methylbenzylamine 97%
CAS:
698-19-1
MF:
C8H10BrN
MW:
200.08
Product Categories:
  • Polyamines
Mol File:
698-19-1.mol
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(2-BROMOBENZYL)METHYLAMINE Chemical Properties

Boiling point:
71-74 °C2 mm Hg(lit.)
Density 
1.358 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.5670(lit.)
Flash point:
220 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Viscous Liquid
pka
9.14±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
Sensitive 
Air Sensitive
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
2
HazardClass 
8

MSDS

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(2-BROMOBENZYL)METHYLAMINE Usage And Synthesis

Synthesis

6630-33-7

698-19-1

Preparation of Example (Compound 22a): 29.4 g of o-bromobenzaldehyde and 81 mL of 40% aqueous methylamine were mixed with 238 mL of tetrahydrofuran (THF). At room temperature, 19 g of sodium borohydride (NaBH4) was added in batches over 25 minutes. The reaction mixture was stirred overnight at room temperature and then concentrated using a rotary evaporator. The residue was stirred into ice water and the aqueous phase was extracted twice with ether. The combined ether phases were concentrated by evaporation under reduced pressure. The product was purified by silica gel column chromatography using ethyl acetate or ethyl acetate/methanol (4:1) as eluent to give 18.5 g of N-methyl-2-bromobenzylamine (22a) in yellow liquid form. Yield: 58%.

References

[1] Patent: US6232468, 2001, B1
[2] Tetrahedron, 2003, vol. 59, # 40, p. 8049 - 8056

(2-BROMOBENZYL)METHYLAMINESupplier

Creasyn Finechem(Tianjin) Co., Ltd.
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Energy Chemical
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