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Merck
CN

191736

Pargyline 盐酸盐

99%

别名:

N-甲基-N-2-丙炔基苄胺 盐酸盐, N-甲基-N-丙炔基苄胺 盐酸盐

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关于此项目

线性分子式:
C6H5CH2N(CH3)CH2C≡CH·HCl
化学文摘社编号:
分子量:
195.69
EC Number:
206-175-1
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
3699487
MDL number:
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assay

99%

mp

160-163 °C (lit.)

SMILES string

Cl[H].CN(CC#C)Cc1ccccc1

InChI

1S/C11H13N.ClH/c1-3-9-12(2)10-11-7-5-4-6-8-11;/h1,4-8H,9-10H2,2H3;1H

InChI key

BCXCABRDBBWWGY-UHFFFAOYSA-N

Gene Information

Biochem/physiol Actions

选择性 MAO-B 抑制剂。


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Masahiro Yoshida et al.
The Journal of organic chemistry, 78(4), 1687-1692 (2013-02-01)
The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively synthesized, respectively.
Highly stereoselective synthesis of tertiary propargylic centers and their isomerization to enantiomerically enriched allenes.
José Luis García Ruano et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(32), 9775-9779 (2012-08-01)
Francesca Reineri et al.
Journal of the American Chemical Society, 134(27), 11146-11152 (2012-06-06)
(15)N-Propargylcholine has been synthesized and hydrogenated with para-H(2). Through the application of a field cycling procedure, parahydrogen spin order is transferred to the (15)N resonance. Among the different isomers formed upon hydrogenation of (15)N-propargylcholine, only the nontransposed derivative contributes to