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334774

N-Methylhomoveratrylamine

Name: <I>N</I>-Methylhomoveratrylamine
Brand: ALDRICH

97%

Synonym(s):

3,4-Dimethoxy-N-methylphenethylamine

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About This Item

Linear Formula:

(CH₃O)₂C₆H₃CH₂CH₂NHCH₃

CAS Number:

3490-06-0

Molecular Weight:

195.26

EC Number:

222-483-9

MDL number:

MFCD00067696

UNSPSC Code:

12352100

PubChem Substance ID:

24860255

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assay

97%

drug control

USDEA Schedule I

refractive index

n20/D 1.533 (lit.)

bp

160-161 °C/13 mmHg (lit.)

density

1.059 g/mL at 25 °C (lit.)

SMILES string

CNCCc1ccc(OC)c(OC)c1

InChI

1S/C11H17NO2/c1-12-7-6-9-4-5-10(13-2)11(8-9)14-3/h4-5,8,12H,6-7H2,1-3H3

InChI key

HNJWKRMESUMDQE-UHFFFAOYSA-N

Application

N-Methylhomoveratrylamine was used in the preparation of:

5,6-dimethoxy-1-oxo-isoindoline derivatives[1]
N-{4-[2-hydroxy-3-(3,4-dimethoxy-N-methylphenylethylamino)propoxy]phenyl}-5,6-dimethoxy-1-oxo-isoindoline[1]
cis[3-[2-[2-(3,4-dimethoxyphenyl)ethyl]methylamino]cyclohexyl]diphenylacetonitrile[2]

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Synthesis of 4-(1-oxo-isoindoline) and 4-(5,6-dimethoxy-1-oxo-isoindoline)-substituted phenoxypropanolamines and their beta1-, beta2-adrenergic receptor binding studies.

Dharam P Jindal et al.

Bioorganic chemistry, 33(4), 310-324 (2005-06-25)

Phenoxypropanolamines with 1-oxo-isoindoline and 5,6-dimethoxy-1-oxo-isoindoline groups at the para position were synthesized. beta1, beta2-Adrenergic receptor binding affinities for the synthesized compounds were tested and compared with propranolol and atenolol. It was found that the incorporation of para-amidic functionality within the

Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators.

Silvia Dei et al.

Bioorganic & medicinal chemistry, 13(4), 985-998 (2005-01-27)

A series of compounds with a diphenylmethyl cyclohexyl skeleton, loosely related to verapamil, has been synthesized and tested as MDR modulators on anthracycline-resistant erythroleukemia K 562 cells. Their residual cardiovascular action (negative inotropic and chronotropic activity as well as vasorelaxant

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