2,4,6-Trimethoxybenzylamine hydrochloride

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Names

[ CAS No. ]:
146548-59-6

[ Name ]:
2,4,6-Trimethoxybenzylamine hydrochloride

[Synonym ]:
(2,4,6-trimethoxyphenyl)methanamine,hydrochloride
MFCD00012855
Benzenemethanamine, 2,4,6-trimethoxy-, hydrochloride (1:1)
(2,4,6-Trimethoxyphenyl)methanamine hydrochloride
1-(2,4,6-Trimethoxyphenyl)methanamine hydrochloride (1:1)

Chemical & Physical Properties

[ Density]:
1.087g/cm3

[ Boiling Point ]:
312ºC at 760mmHg

[ Melting Point ]:
204-207 °C(lit.)

[ Molecular Formula ]:
C10H16ClNO3

[ Molecular Weight ]:
233.692

[ Flash Point ]:
151.1ºC

[ Exact Mass ]:
233.081863

[ PSA ]:
53.71000

[ LogP ]:
2.67340

[ Vapour Pressure ]:
0.000544mmHg at 25°C

[ Index of Refraction ]:
1.515

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38:Irritating to eyes, respiratory system and skin .

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Facile synthesis of 3-(aminomethyl)isoquinolines by copper-catalysed domino four-component coupling and cyclisation.

Chem. Commun. (Camb.) (7) , 835-7, (2008)

Copper(i)-catalysed domino four-component coupling-cyclisation using 2-ethynylbenzaldehydes, paraformaldehyde, secondary amine, and t-BuNH(2) in DMF leads to direct and efficient formation of 3-(amino...


More Articles


Related Compounds

  • 2,4,6-trimethoxybenzylamine hydrochloride
  • 2,4,6-TRIMETHOXYBENZYLAMINE
  • 1,2,6-Trimethyl-4-phenyl-4-pyperidinol propionata (2,4,6) hydrochloride
  • 2,4,6-Trimethoxyaniline (Hydrochloride)
  • 2,4,6-triethylaniline,hydrochloride
  • 2,4,6-TRIMETHYLANILINE HYDROCHLORIDE
  • 2-(2,3-Dihydroindol-1-yl)-6-(4-methyl-2-piperidin-1-ylpyrimidin-5-yl)-1,3-diazinan-4-one
  • N-[(3,4-dimethoxyphenyl)methyl]-3-[2-(4-fluorophenyl)-4-oxo-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrazin-5-yl]propanamide
  • (R)-[Ethoxy(phenyl)phosphoryl](phenyl)methyl butanoate
  • N-(2-(3-(pyridin-4-yl)-1H-pyrazol-1-yl)ethyl)furan-2-carboxamide
  • 3-[2-(4-fluorophenyl)-4-oxo-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrazin-5-yl]-N-[(4-methylsulfanylphenyl)methyl]propanamide
  • 2-(benzylthio)-N-(2-(3-(pyridin-2-yl)-1H-pyrazol-1-yl)ethyl)acetamide
  • 1-(1-(4-fluorobenzyl)-1H-benzo[d]imidazol-2-yl)pyrrolidin-3-ol
  • 4-(3,4-Dihydroxyphenyl)-6-[(3,4-dihydroxyphenyl)methylene]-3-hydroxy-2H-pyran-2,5(6H)-dione
  • 1-((3-(Bromomethyl)phenyl)sulfonyl)pyrrolidin-3-ol
  • N-[(2,4-difluorophenyl)methyl]-3-[2-(4-fluorophenyl)-4-oxo-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrazin-5-yl]propanamide
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