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N-Methylhomoveratrylamine

Names

[ CAS No. ]:
3490-06-0

[ Name ]:
N-Methylhomoveratrylamine

[Synonym ]:
MFCD00067696
N-methyl-2-(3,4-dimethoxy-phenyl)-ethylamine
EINECS 222-483-9
N-Methylhomoveratrylamine
2-(2'-N-BOC-PYRROLE)BENZOIC ACID
[2-(3,4-Dimethoxyphenyl)Ethyl](Methyl)Amine
3,4-dimethoxy-N-methylphenethylamine
2-(3,4-dimethoxyphenyl)-N-methyl-1-ethaneamine
N-methyl-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-amine
2-(3,4-DiMethoxyphenyl)-N-MethylethylaMine
N-methyl-3,4-dimethoxyphenethylamine

Chemical & Physical Properties

[ Density]:
1.059 g/mL at 25 °C(lit.)

[ Boiling Point ]:
160-161 °C13 mm Hg(lit.)

[ Molecular Formula ]:
C11H17NO2

[ Molecular Weight ]:
195.25800

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
195.12600

[ PSA ]:
30.49000

[ LogP ]:
1.85660

[ Index of Refraction ]:
n20/D 1.533(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
1760

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2922299090

Customs

[ HS Code ]: 2922299090

[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

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

Bioorg. Med. Chem. 13(4) , 985-98, (2005)

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....

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

Bioorg. Chem. 33(4) , 310-24, (2005)

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 c...


More Articles


Related Compounds

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