Basic information Safety Supplier Related

(3,4-Dichlorobenzyl)methylamine

Basic information Safety Supplier Related

(3,4-Dichlorobenzyl)methylamine Basic information

Product Name:
(3,4-Dichlorobenzyl)methylamine
Synonyms:
  • 1-(3,4-Dichlorophenyl)-N-MethylMethanaMine
  • 1-(3,4-Dichlorophenyl)
  • (3,4-dichlorophenyl)methyl-methylammonium
  • Olanexidine Impurity 7
  • N-(3,4-DICHLOROBENZYL)-N-METHYLAMINE
  • 3,4-DICHLORO-N-METHYLBENZYLAMINE
  • (3,4-DICHLOROBENZYL)METHYLAMINE
  • N-(3,4-Dichlorobenzyl)-N-methylamine ,97%
CAS:
5635-67-6
MF:
C8H9Cl2N
MW:
190.07
Mol File:
5635-67-6.mol
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(3,4-Dichlorobenzyl)methylamine Chemical Properties

Boiling point:
146 °C(Press: 47 Torr)
Density 
1.226±0.06 g/cm3(Predicted)
storage temp. 
2-8°C, protect from light
pka
8.77±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

HS Code 
2921490090
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(3,4-Dichlorobenzyl)methylamine Usage And Synthesis

Synthesis

6287-38-3

74-89-5

5635-67-6

General procedure for the synthesis of N-(3,4-dichlorobenzyl)-N-methylamine from 3,4-dichlorobenzaldehyde and methylamine: 3,4-dichlorobenzaldehyde (600 mg, 3.43 mmol, 1.0 eq.) was mixed with methylamine (0.64 mL, 5.14 mmol, 8.03 M in ethanol, 1.5 eq.) in anhydrous 1,2-dichloroethane (12 mL) and stirred under nitrogen protection for 3 hours. Subsequently, sodium triacetoxyborohydride (1.02 g, 4.81 mmol, 1.4 eq.) was added and the reaction mixture continued to be stirred at room temperature for 18 hours. Upon completion of the reaction, the mixture was poured into 2 M aqueous sodium carbonate solution and extracted with ethyl acetate (3 x 10 mL). The organic phases were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure. Finally, the product was purified by silica gel column chromatography with the eluent methanol:methanol:dichloromethane containing 7N ammonia (the ratio was gradually changed from 1:5:94 to 1:10:89 and finally 1:15:84) to give a light yellow oily product (455 mg, 70% yield).

References

[1] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 11, p. 3016 - 3020
[2] Journal of Medicinal Chemistry, 1981, vol. 24, # 2, p. 140 - 145

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