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250996

Sigma-Aldrich

2-Chloro-N,N-diethylacetamide

97%

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About This Item

Linear Formula:
ClCH2CON(C2H5)2
CAS Number:
Molecular Weight:
149.62
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.47 (lit.)

bp

148-150 °C/55 mmHg (lit.)

density

1.089 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

SMILES string

CCN(CC)C(=O)CCl

InChI

1S/C6H12ClNO/c1-3-8(4-2)6(9)5-7/h3-5H2,1-2H3

InChI key

CQQUWTMMFMJEFE-UHFFFAOYSA-N

Application

2-Chloro-N,N-diethylacetamide has been used in:
  • preparation of calixarene amides
  • synthesis of 5-bromo-25,26,27,28-tetrakis[(N,N-diethylaminocarbonyl)-methoxy]calix[4]arene
  • synthesis of amide calix[4]pyrrole macrocycles with super-extended cavities
  • microwave-assisted organic synthesis of 3-cyano-N,N-diethyl-4-(4-methoxyphenoyl)-4-oxobutanamide

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °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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[Local and skin resorptive action of N,N-diethylchloracetamide].
V A Shugaev et al.
Gigiena truda i professional'nye zabolevaniia, (2)(2), 51-52 (1989-01-01)
Synthesis and properties of new calixarene-based ditopic receptors for the simultaneous complexation of cations and carboxylate anions.
Pelizzi N, et al.
J. Chem. Soc. Perkin Trans. II, 6, 1307-1312 (1998)
[Gas-chromatographic analysis of N,N-diethylchloracetamide in the air].
L P Shcherbakov et al.
Gigiena i sanitariia, (5)(5), 57-59 (1989-05-01)
Christopher J Woods et al.
Journal of the American Chemical Society, 124(29), 8644-8652 (2002-07-18)
A new "super-extended cavity" tetraacetylcalix[4]pyrrole derivative was synthesized and characterized, and X-ray crystal structures of complexes bound to fluoride and acetonitrile were obtained. The binding behavior of this receptor was investigated by NMR titration, and the complex was found to
Synthesis and crystal structures of lower rim amine and carbamoyl substituted calixarenes as transfer agents for oxyanions between an aqueous and a chloroform phase.
Wolf NJ, et al.
Polyhedron, 18(6), 855-896 (1999)

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