ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Pyridine compound Pyridine derivatives METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE

METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE

METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE Basic information
Product Name:METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE
Synonyms:2-Pyridinemethanamine, N-methyl-;N-Methyl(2-pyridinyl)methanamine;Pyridine, 2-(methylaminomethyl)-;N-Methyl-N-(2-pyridinylmethyl)amine;METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE;methyl(2-pyridylmethyl)amine;2-[Methyl(aminomethyl)]pyridine dihydrochloride;2-[(Methylamino)methyl]pyridine
CAS:21035-59-6
MF:C7H10N2
MW:122.17
EINECS:244-160-1
Product Categories:Aminomethyl's;Pyridines
Mol File:21035-59-6.mol
METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE Structure
METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE Chemical Properties
Melting point 64 °C
Boiling point 78-80 °C(Press: 10 Torr)
density 0.994 g/mL at 25 °C
refractive index n20/D1.524
Fp 82℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pkapK1:2.92(＋2);pK2:8.82(＋1) (30°C)
form liquid
color Colorless
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-37/38-41
Safety Statements 26
WGK Germany 3
HazardClass IRRITANT
HS Code 2933399990
MSDS Information
METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE Usage And Synthesis
Uses2-[(Methylamino)methyl]pyridine is used as a reagent in the preparation and structure activity relationship of imidazolopyrimidones as gonadotropin-releasing hormone (GnRH) receptor antagonists.
METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE Preparation Products And Raw materials
(1-phenylpropyl)(pyridin-2-ylmethyl)amine 4-(1,3-DIOXO-1,3-DIHYDRO-2H-INDEN-2-YLIDEN)-2-PHENYL-6-(2-PYRIDINYL)TETRAHYDROPYRROLO[3,4-C]PYRROLE-1,3(2H,3AH)-DIONE 2-(1-Piperidinylmethyl)-3-pyridinol 10-Hydroxycamptothecin TPEN 2-(Dimethylaminomethyl)-3-hydroxypyridine N2-[2-CHLORO-6-(([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDYL]CARBONYL)AMINO)-4-(TRIFLUOROMETHYL)PHENYL]-3-CHLORO-5-(TRIFLUOROMETHYL)PYRIDINE-2-CARBOXAMIDE 3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHYL)-1-[[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL](METHYL)AMINO]-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE [3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL](4-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]PIPERAZINO)METHANONE OXIME 1-(4-CHLOROPHENYL)-3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHYL)-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE N2-[4-CHLORO-2-(([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDYL]CARBONYL)AMINO)-5-FLUOROPHENYL]-3-CHLORO-5-(TRIFLUOROMETHYL)PYRIDINE-2-CARBOXAMIDE 3-CHLORO-N-(4-CHLOROPHENYL)-N'-HYDROXY-5-(TRIFLUOROMETHYL)-2-PYRIDINECARBOXIMIDAMIDE 1-(4-CHLOROBENZYL)-3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHYL)-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE 1-(2-CHLOROPHENYL)-N-METHYL-N-(1-METHYLPROPYL)-3-ISOQUINOLINECARBOXAMIDE 2-(BIS-(2-PYRIDYLMETHYL)-AMINO)-ETHANOL 6-METHYL-2-PICOLYL-METHYLAMINE 3-CHLORO-N-(4-CHLOROBENZYL)-N'-HYDROXY-5-(TRIFLUOROMETHYL)-2-PYRIDINECARBOXIMIDAMIDE 2-(2-ETHYLHEXYLAMINOMETHYL)PYRIDINE DIHYDROCHLORIDE
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