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C65408

Sigma-Aldrich

2-(4-Chlorophenyl)ethylamine

98%

Sinónimos:

4-Chlorophenethylamine

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About This Item

Fórmula lineal:
ClC6H4CH2CH2NH2
Número de CAS:
156-41-2
Peso molecular:
155.62
Beilstein/REAXYS Number:
508247
EC Number:
205-853-4
MDL number:
MFCD00008191
UNSPSC Code:
12352100
PubChem Substance ID:
24892877
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.548 (lit.)

bp

60-65 °C/0.1 mmHg (lit.)

density

1.112 g/mL at 25 °C (lit.)

SMILES string

NCCc1ccc(Cl)cc1

InChI

1S/C8H10ClN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2

InChI key

SRXFXCKTIGELTI-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

222.8 °F - closed cup

flash_point_c

106 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
SHBM3949
SHBD0161V
65997PJV
65997PJ
04404EH

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Marina Marani et al.
Oncotarget, 7(4), 4570-4583 (2015-12-31)
Serine hydroxymethyltransferase (SHMT) is a central enzyme in the metabolic reprogramming of cancer cells, providing activated one-carbon units in the serine-glycine one-carbon metabolism. Previous studies demonstrated that the cytoplasmic isoform of SHMT (SHMT1) plays a relevant role in lung cancer.
Giulia Guiducci et al.
Nucleic acids research, 47(8), 4240-4254 (2019-02-28)
Enzymes of intermediary metabolism are often reported to have moonlighting functions as RNA-binding proteins and have regulatory roles beyond their primary activities. Human serine hydroxymethyltransferase (SHMT) is essential for the one-carbon metabolism, which sustains growth and proliferation in normal and
G B Baker et al.
Progress in neuro-psychopharmacology & biological psychiatry, 6(4-6), 343-346 (1982-01-01)
1. The accumulation of p-chlorophenylethylamine (pCPE) in rat brain after administration of pargyline plus p-chlorophenylalanine (pCPA) is demonstrated. 2. Measurements of pCPE in brain were performed at 0.25 h, 1 h and 4 h after administration of pCPA to pargyline-pretreated
Khalid Touiki et al.
Psychopharmacology, 182(4), 562-569 (2005-09-01)
Harmane and norharmane (two beta-carbolines) are tobacco components or products. The effects of harmane and norharmane on serotonergic raphe neurons remain unknown. Harmane and norharmane are inhibitors of the monoamine oxidases A (MAO-A) and B (MAO-B), respectively. To study the
D Becquet et al.
Neuroscience, 39(3), 639-647 (1990-01-01)
Using a push-pull cannula technique and an isotopic method for estimating [3H]serotonin continuously synthesized from [3H]tryptophan, the effects of changes in the release of serotonin in the dorsalis raphe nucleus on in vivo release of [3H]serotonin in the cat caudate
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