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Merck
CN

334774

N-Methylhomoveratrylamine

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
UNSPSC Code:
12352100
PubChem Substance ID:
24860255
EC Number:
222-483-9
MDL number:
MFCD00067696

Key Documents

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InChI key

HNJWKRMESUMDQE-UHFFFAOYSA-N

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

SMILES string

CNCCc1ccc(OC)c(OC)c1

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.)

Application

N-Methylhomoveratrylamine was used in the preparation of:
  • 5,6-dimethoxy-1-oxo-isoindoline derivatives
  • N-{4-[2-hydroxy-3-(3,4-dimethoxy-N-methylphenylethylamino)propoxy]phenyl}-5,6-dimethoxy-1-oxo-isoindoline
  • cis[3-[2-[2-(3,4-dimethoxyphenyl)ethyl]methylamino]cyclohexyl]diphenylacetonitrile

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
S40752
13918KS
13502LS
06620DO
04712AN

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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
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

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