N-Methylpropargylamine - CAS 35161-71-8

Catalog:	BB022512
Product Name:	N-Methylpropargylamine
CAS:	35161-71-8
Synonyms:	N-methylprop-2-yn-1-amine

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	N-methylprop-2-yn-1-amine
Description:	N-Methylpropargylamine (CAS# 35161-71-8) is a metabolite of Pargyline. N-Methylpropargylamine, like other propynylamine, has inhibitory effect on monoamine oxidase.
Molecular Weight:	69.11
Molecular Formula:	C4H7N
Canonical SMILES:	CNCC#C
InChI:	InChI=1S/C4H7N/c1-3-4-5-2/h1,5H,4H2,2H3
InChI Key:	HQFYIDOMCULPIW-UHFFFAOYSA-N
Boiling Point:	83.9 °C at 760 mmHg
Purity:	95 %
Density:	0.819 g/cm³
Appearance:	Clear liquid
Storage:	2-8 °C
MDL:	MFCD00008573
LogP:	0.22990

Publication Number	Title	Priority Date
CN-113121521-A	6-trifluoromethyl-substituted benzothiazinone derivative and preparation method and application thereof	20210326
CN-111675808-A	Holographic photopolymer material based on two-stage sulfydryl-alkyne polymerization reaction	20200623
CN-111269197-A	Benzothiazinone compound, preparation method thereof and application of compound as antituberculosis drug	20200408
CN-112409293-A	Benzothiazinone compound, preparation method thereof and application of compound as antituberculosis drug	20200408
WO-2021203811-A1	Benzothiazinone compound, preparation method therefor and application thereof as anti-tuberculosis drug	20200408

PMID	Publication Date	Title	Journal
21669479	20110901	Synthesis, biological assessment and molecular modeling of new multipotent MAO and cholinesterase inhibitors as potential drugs for the treatment of Alzheimer's disease	European journal of medicinal chemistry
18771016	20080301	[A comparison of the pharmacology of (-)-deprenyl to N-methylpropargylamine-1-aminoindane (J-508) and rasagiline, the desmethyl-analogue of J-508]	Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology
15843867	20060101	N-Propargylamine protects SH-SY5Y cells from apoptosis induced by an endogenous neurotoxin, N-methyl(R)salsolinol, through stabilization of mitochondrial membrane and induction of anti-apoptotic Bcl-2	Journal of neural transmission (Vienna, Austria : 1996)
12360928	20020902	Diphosphanylketenimines: new reagents for the synthesis of unique phosphorus heterocycles	Chemistry (Weinheim an der Bergstrasse, Germany)

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Related Functional Groups

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[926-55-6]
2-Methyl-1-penten-3-yne

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GHS Hazard Statement:	H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
Precautionary Statement:	P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, and P501
Signal Word:	Danger

Complexity:	47.9
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	69.057849228
Formal Charge:	0
Heavy Atom Count:	5
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	69.057849228
Rotatable Bond Count:	1
Topological Polar Surface Area:	12 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-0.1