Recommended Products
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
Related Categories
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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[Gas-chromatographic analysis of N,N-diethylchloracetamide in the air].
Gigiena i sanitariia, (5)(5), 57-59 (1989-05-01)
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.
Polyhedron, 18(6), 855-896 (1999)
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.
[Local and skin resorptive action of N,N-diethylchloracetamide].
Gigiena truda i professional'nye zabolevaniia, (2)(2), 51-52 (1989-01-01)
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