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Merck
CN

250996

2-Chloro-N,N-diethylacetamide

97%

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About This Item

Linear Formula:
ClCH2CON(C2H5)2
CAS Number:
Molecular Weight:
149.62
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-019-2
MDL number:
Assay:
97%
Form:
liquid
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Product Name

2-Chloro-N,N-diethylacetamide, 97%

InChI key

CQQUWTMMFMJEFE-UHFFFAOYSA-N

InChI

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

SMILES string

CCN(CC)C(=O)CCl

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

Quality Level

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

signalword

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

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

ppe

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


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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)
[Data on hygienic standardization of N,N-diethyl-2-chloroacetamide in the air of the work area].
V A Shugaev et al.
Gigiena truda i professional'nye zabolevaniia, (6)(6), 36-37 (1991-01-01)
Dewei Tang et al.
Tetrahedron letters, 51(35), 4595-4598 (2010-08-07)
We herein report a dramatically improved total synthesis of the high-affinity translocator protein (TSPO) ligand DPA-714, featuring microwave-assisted organic synthesis (MAOS). Compared with previously described approaches, our novel MAOS method dramatically reduces overall reaction time without adversely effecting reaction yields.
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)
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)

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