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300985

Sigma-Aldrich

2,4,6-Trimethoxybenzylamine hydrochloride

98%

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About This Item

Linear Formula:
(CH3O)3C6H2CH2NH2·HCl
CAS Number:
146548-59-6
Molecular Weight:
233.69
MDL number:
MFCD00012855
UNSPSC Code:
12352100
PubChem Substance ID:
24858152
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

204-207 °C (lit.)

SMILES string

Cl.COc1cc(OC)c(CN)c(OC)c1

InChI

1S/C10H15NO3.ClH/c1-12-7-4-9(13-2)8(6-11)10(5-7)14-3;/h4-5H,6,11H2,1-3H3;1H

InChI key

BLFRMOOGAICNSZ-UHFFFAOYSA-N

Application

2,4,6-Trimethoxybenzylamine hydrochloride was used in synthesis of 3-(aminomethyl)isoquinoline.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Yusuke Ohta et al.
Chemical communications (Cambridge, England), (7)(7), 835-837 (2008-02-07)
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-(aminomethyl)isoquinolines in good to high yields.

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