Skip to main content

3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide

ADVERTISEMENT
Identification
Molecular formula
C12H11Cl2NO
CAS number
101389-84-4
IUPAC name
3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide
State
State

At room temperature, 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide is a solid.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
518.90
Boiling point (Kelvin)
792.05
General information
Molecular weight
255.12g/mol
Molar mass
255.1160g/mol
Density
1.3030g/cm3
Appearence

3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide is a solid compound. Its appearance typically includes a crystalline structure and is often encountered as a powder. The solid is generally white to off-white in color.

Comment on solubility

Solubility of 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide

The solubility of 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide is a critical factor in its application and behavior in various environments. Understanding its solubility can provide insights into its potential uses and interactions. Here are some key points regarding the solubility of this compound:

  • Solvent Compatibility: Generally, this compound is expected to exhibit moderate solubility in organic solvents such as ethanol, acetone, and dichloromethane, while being poorly soluble in polar solvents like water.
  • Influence of Substituents: The presence of chloro groups can affect the solubility profile by influencing the overall polarity and hydrogen bonding capacity of the molecule.
  • Temperature Effects: Like many organic compounds, the solubility may increase with temperature due to enhanced molecular movement, potentially improving its dissolution rates in suitable solvents.
  • Concentration Dependent: At higher concentrations, one may observe a decrease in solubility due to the compound reaching its saturation point.

In conclusion, the solubility characteristics of 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide imply that it is more suited for applications in non-polar or mildly polar solvents rather than in aqueous environments. This highlights the importance of selecting the right solvent system in experiments and formulations involving this compound.

Interesting facts

Interesting Facts about 3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide

3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide is a fascinating compound known for its unique structural characteristics and applications in various fields. Here are some intriguing aspects of this chemical:

  • Biological Activity: The compound has been studied for its potential therapeutic effects, particularly in the realm of pharmaceutical chemistry. Its formulation often explores its capacity as a selective inhibitor, which can be crucial in the development of targeted treatments.
  • Structural Complexity: This compound contains a benzamide moiety, which is associated with numerous biologically active agents. The presence of multiple chlorine atoms enhances its reactivity and allows for a diversified range of chemical interactions, making it a molecule of interest for synthetic chemists.
  • Synthesis Considerations: The synthesis of 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide can involve intricate multi-step reactions, illustrating the creativity required in organic synthesis. Researchers often utilize this compound as a benchmark for new synthetic strategies.
  • Applications in Agrochemicals: Beyond pharmaceuticals, there is a growing interest in this compound's potential use in agrochemicals. The chlorinated structure could provide the stability and efficacy needed for pest control formulations.
  • Research Implications: Scientists are continually exploring the implications of variations within the compound's structure. Studies may focus on modifying the groups attached to the benzamide, which can result in compounds with significantly different properties and activities.

As noted by a renowned chemist, "Understanding the nuances of molecular interactions at this level is what drives innovation." This sentiment rings true with compounds like 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide, as they represent the intersection of creativity and rigorous scientific inquiry.

In the context of materials science, this compound demonstrates how synthetic modifications can lead to enhanced material properties, paving the way for future research and applications.

Synonyms
Propyzamide
23950-58-5
PRONAMIDE
3,5-Dichloro-N-(1,1-dimethylpropynyl)benzamide
3,5-dichloro-N-(2-methylbut-3-yn-2-yl)benzamide
KERB
Pronamid
Clanex
3,5-Dichloro-N-(1,1-dimethyl-2-propynyl)benzamide
KERB 50W
3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide
RH 315
N-(1,1-Dimethylpropynyl)-3,5-dichlorobenzamide
Benzamide, 3,5-dichloro-N-(1,1-dimethyl-2-propynyl)-
DTXSID2020420
RH-315
CHEBI:34935
2EZ95375S0
DTXCID80420
propisamide
propizamide
RefChem:176569
245-951-4
MFCD00055346
Promamide
3,5-Dichloro(N-1,1-dimethyl-2-propynyl)benzamide
Propyzamide 10 microg/mL in Cyclohexane
Propyzamide 100 microg/mL in Acetonitrile
Propyzamide, analytical standard
3,5-dichloro-N-(1,1-dimethyl-2-propyn-1-yl)benzamide
3,5-dichloro-N-(1,1-dimethylprop-2-yn-1-yl)benzamide
Caswell No. 306A
Propyzamide [BSI:ISO]
RCRA waste number U192
Pronamide (Kerb)
Propyzamide [ISO]
CAS-23950-58-5
CCRIS 1413
HSDB 5118
EINECS 245-951-4
RCRA waste no. U192
EPA Pesticide Chemical Code 101701
BRN 0882391
Rustler
UNII-2EZ95375S0
Kerb Flo
Campbell's rapier
Kerb propyzamide 50
PROPYZAMIDE [MI]
PROPYZAMIDE [HSDB]
SCHEMBL55124
3,5-Dichloro-N-(2-methyl-3-butyn-2-yl)benzamide
BIDD:ER0426
3,5-Dichloro-N-(1,1-dimethyl-2-propynyl) benzamide
CHEMBL283487
orb1182340
PHNUZKMIPFFYSO-UHFFFAOYSA-
CS-D1356
MSK22387
Tox21_201413
Tox21_301164
AKOS010651566
Pronamide (Kerb), analytical standard
DS-1304
NCGC00168331-01
NCGC00168331-02
NCGC00168331-03
NCGC00255062-01
NCGC00258964-01
SY030062
NS00000560
P2374
Propyzamide, PESTANAL(R), analytical standard
950P585
F079658
N- (1',1'-dimethylpropynyl)-3,5-dichlorobenzamide
N-(1',1'-dimethylpropynyl)-3,5-dichlorobenzamide
N-(1,1-dimethyl-2-propynyl)-3,5-dichlorobenzamide
Q2113173
InChI=1/C12H11Cl2NO/c1-4-12(2,3)15-11(16)8-5-9(13)7-10(14)6-8/h1,5-7H,2-3H3,(H,15,16)