Skip to Content
Merck
All Photos(1)

Documents

560421

Sigma-Aldrich

3,4-Dichlorophenethylamine

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
Cl2C6H3CH2CH2NH2
CAS Number:
Molecular Weight:
190.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.567 (lit.)

bp

280 °C (lit.)

density

1.268 g/mL at 25 °C (lit.)

SMILES string

NCCc1ccc(Cl)c(Cl)c1

InChI

1S/C8H9Cl2N/c9-7-2-1-6(3-4-11)5-8(7)10/h1-2,5H,3-4,11H2

InChI key

MQPUAVYKVIHUJP-UHFFFAOYSA-N

Related Categories

General description

3,4-Dichlorophenethylamine can be obtained by reacting 3,4-dichlorophenylacetonitrile with suspension of lithium aluminum hydride (LiAlH4) in dry diethyl ether in the presence of N2.

Application

3,4-Dichlorophenethylamine may be used to synthesize N-(3′,4′-dichlorophenyl)ethyl-4-azahexacyclo[5.4.1.02,6.03,10.05,9.08,11]dodecan-3-ol and 2-[2-(3,4-dichlorophenyl)ethylamino]-1-pyridin-3-ylethanol.

Caution

Absorbs CO2 from Air

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis, Conformation, and Stereodynamics of a Salt of 2-{[2-(3, 4-Dichlorophenyl)-ethyl] propylamino}-1-pyridin-3-ylethanol.
Korosec T, et al.
The Journal of Organic Chemistry, 71(2), 792-795 (2006)
Xiang Liu et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 1(1), 31-38 (2006-06-23)
Three new trishomocubane analogues based on the 4-azahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)] dodecane-3-ol skeleton have been synthesised and assessed for their affinities at both sigma-1 and sigma-2 receptors. The effect of various N-substitution on the polycyclic moiety was examined. All synthesised compounds displayed high

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service