Skip to main content

N,N-diallyl-2-chloroacetamide

ADVERTISEMENT
Identification
Molecular formula
C8H12ClNO
CAS number
21551-62-2
IUPAC name
N,N-diallyl-2-chloro-acetamide
State
State

At room temperature, N,N-diallyl-2-chloroacetamide is typically in a liquid state. It remains stable under standard atmospheric conditions and does not readily evaporate.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
175.65g/mol
Molar mass
175.6500g/mol
Density
1.0930g/cm3
Appearence

N,N-diallyl-2-chloroacetamide appears as a clear to pale yellow liquid. Its appearance in bulk is generally homogeneous without any noticeable particulate matter. It may exhibit a faint, characteristic odor.

Comment on solubility

Solubility of N,N-diallyl-2-chloro-acetamide

N,N-diallyl-2-chloro-acetamide, with the chemical formula C7H10ClN1O1, exhibits intriguing solubility characteristics that warrant attention. This compound is primarily soluble in organic solvents due to its structural properties. Here is a breakdown of its solubility behavior:

  • Polar Solvents: N,N-diallyl-2-chloro-acetamide shows limited solubility in polar solvents such as water, which can be attributed to its hydrophobic diallyl groups.
  • Non-Polar Solvents: The compound is well-soluble in non-polar solvents like hexane or ethyl acetate, highlighting its affinity for organic environments.
  • Temperature Influence: Like many organic compounds, solubility tends to increase with temperature, suggesting that heating may enhance dissolution in applicable solvents.
  • pH Dependence: The solubility may also be influenced by the pH of the solution, but specific data might vary according to the conditions.

In summary, while N,N-diallyl-2-chloro-acetamide is somewhat challenged by solubility in water, it is quite compatible with a variety of organic solvents. This behavior is essential for its practical applications in organic synthesis and pharmaceutical formulation.

Interesting facts

Interesting Facts about N,N-diallyl-2-chloro-acetamide

N,N-diallyl-2-chloro-acetamide is a fascinating compound with various applications and characteristics that make it noteworthy in the field of chemistry.

Key Characteristics and Applications

  • Versatile Chemical Building Block: This compound serves as an important intermediate in organic synthesis. It is often used to create more complex molecules.
  • Polymers and Resins: N,N-diallyl-2-chloro-acetamide is utilized in producing polymers and resins, contributing to materials with diverse functionalities.
  • Potential in Agriculture: Several studies suggest that compounds like N,N-diallyl-2-chloro-acetamide may have uses in agrochemicals, such as herbicides or pesticides, helping to enhance agricultural productivity.
  • Pharmaceutical Applications: This compound’s reactivity can be of interest in the pharmaceutical industry, as it may lead to the development of new therapeutic agents.

Chemical Properties and Reactivity

  • Electrophilic Nature: The presence of the chloro group in its structure makes it an electrophile, allowing it to participate in various chemical reactions.
  • Potential for Crosslinking: Its diallyl groups can engage in free radical polymerization, an essential aspect for creating crosslinked polymer networks.

As a chemistry student or scientist, understanding the properties and potential applications of N,N-diallyl-2-chloro-acetamide opens doors to exciting research opportunities. The compound not only enhances our knowledge of organic chemistry but also provides practical solutions in various industries, paving the way for innovative advancements.

Synonyms
Allidochlor
93-71-0
N,N-Diallyl-2-chloroacetamide
Alidochlor
CDAA
Alidochlore
RANDOX
2-Chloro-N,N-diallylacetamide
Allidochlor [ISO]
Cdaat
Rantox T
N,N-Diallylchloroacetamide
Diallylchloroacetamide
Caswell No. 284
Acetamide, 2-chloro-N,N-di-2-propenyl-
2-chloro-N,N-bis(prop-2-en-1-yl)acetamide
2-Chloro-N,N-di-2-propenylacetamide
HSDB 1560
2-chloro-N,N-bis(prop-2-enyl)acetamide
NCI-C04035
Acetamide, 2-chloro-N,N-diallyl-
Acetamide, N,N-diallyl-2-chloro-
EINECS 202-270-7
UNII-2E0WF154QR
EPA Pesticide Chemical Code 019301
BRN 1761616
Diallylamid kyseliny chloroctove
CP 6,343
AI3-51490
Acetamide, 2-chloro-N,N-di-2-propen-1-yl-
ALLIDOCHLOR [MI]
ALLIDOCHLOR [HSDB]
N-Diallyl-2-Chloroacetamide
2E0WF154QR
DTXSID2041591
CHEBI:82170
4-04-00-01064 (Beilstein Handbook Reference)
.alpha.-Chloro-N,N-diallylacetamide
N,N-Diallyl-.alpha.-chloroacetamide
CP-6343
Alidochlore; Allidochlor; CDAA; CP 6,343;N,N-Diallylchloroacetamide; Randox
alpha-Chloro-N,N-diallylacetamide
Diallylamid kyseliny chloroctove [Czech]
Radox
N,NDiallylchloroacetamide
2ChloroN,Ndiallylacetamide
N,NDiallyl2chloroacetamide
SCHEMBL53540
Acetamide, 2chloroN,Ndiallyl
Acetamide, N,Ndiallyl2chloro
alphaChloroN,Ndiallylacetamide
2ChloroN,Ndi2propenylacetamide
N,N-diallyl-2-chloro-acetamide
CHEMBL2251312
DTXCID0021591
Acetamide, 2chloroN,Ndi2propenyl
USEPA/OPP PC code 019301
AAA09371
N,N-DIALLYL-2-CHLOREACETAMIDE
AKOS000202499
Allidochlor 100 microg/mL in Methanol
AS-59792
DIALLYLCHLOROACETAMIDE-CHLOTOACETAMIDE
CS-0013971
NS00002977
EN300-08117
Allidochlor, PESTANAL(R), analytical standard
C19043
E79184
Q17310226
Z56899050
F2158-1328
202-270-7