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M74253

Sigma-Aldrich

N-Methyl-N-propargylbenzylamine

97%

Synonyma:

Pargyline

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
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About This Item

Lineární vzorec:
C6H5CH2N(CH3)CH2C≡CH
Číslo CAS:
555-57-7
Molekulová hmotnost:
159.23
EC Number:
209-101-6
MDL number:
MFCD00008576
UNSPSC Code:
12352100
PubChem Substance ID:
24897164
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.522 (lit.)

bp

86-88 °C/4 mmHg (lit.)

density

0.944 g/mL at 25 °C (lit.)

SMILES string

CN(CC#C)Cc1ccccc1

InChI

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

InChI key

DPWPWRLQFGFJFI-UHFFFAOYSA-N

Gene Information

human ... MAOA(4128) , MAOB(4129)

Pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Osvědčení o analýze (COA)

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Lysine-specific demethylase 1 (LSD1, also known as KDM1A and AOF2) is a chromatin-modifying activity that catalyzes the removal of methyl groups from lysine residues in histone and non-histone proteins, regulating gene transcription. LSD1 is overexpressed in several cancer types, and
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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.
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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
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