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243736

Sigma-Aldrich

2-(2-Chlorophenyl)ethylamine

95%

Synonym(s):

2-Chlorophenethylamine

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About This Item

Linear Formula:
ClC6H4CH2CH2NH2
CAS Number:
13078-80-3
Molecular Weight:
155.62
EC Number:
235-982-1
MDL number:
MFCD00008185
UNSPSC Code:
12352100
PubChem Substance ID:
24854634
NACRES:
NA.22

Quality Level

100

Assay

95%

form

liquid

refractive index

n20/D 1.551 (lit.)

bp

120 °C/15 mmHg (lit.)

density

1.106 g/mL at 25 °C (lit.)

SMILES string

NCCc1ccccc1Cl

InChI

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

InChI key

RZBOMSOHMOVUES-UHFFFAOYSA-N

Related Categories

Application

2-(2-Chlorophenyl)ethylamine was used in the synthesis of polymer bound BOC substituted sulfamides.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °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’.

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W Weyler
Archives of biochemistry and biophysics, 255(2), 400-408 (1987-06-01)
The reaction of 2-chloro-2-phenylethylamine with monoamine oxidase B was investigated to study the mechanism of this enzyme and its inactivation by this compound. 2-Chloro-2-phenylethylamine is a substrate with a Km of 30 microM and a turnover number of 80 min-1
Solid-phase synthesis of sulfamides.
Esteve C and Vidal B.
Tetrahedron Letters, 43(6), 1019-1021 (2002)

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