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Isopropylideneamino N-phenylcarbamate

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Identification
Molecular formula
C12H14N2O2
CAS number
2073-34-1
IUPAC name
(isopropylideneamino) N-phenylcarbamate
State
State

At room temperature, Isopropylideneamino N-phenylcarbamate is in a solid state, generally observed as a fine crystalline powder.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
206.25g/mol
Molar mass
206.2500g/mol
Density
1.1500g/cm3
Appearence

Isopropylideneamino N-phenylcarbamate typically appears as a white crystalline solid.

Comment on solubility

Solubility of (isopropylideneamino) N-phenylcarbamate

The solubility of (isopropylideneamino) N-phenylcarbamate can be a complex topic due to its unique chemical structure. This compound is generally classified as a carbamate, which often exhibits diverse solubility properties depending on the solvent used.

In particular, the solubility characteristics of this compound can be summarized as follows:

  • Solvents: It tends to dissolve in polar solvents such as water and alcohols, while being less soluble in non-polar solvents.
  • Influence of Temperature: Temperature can significantly affect solubility; often, increasing temperature enhances the solubility of solid compounds in liquids.
  • pH Sensitivity: The solubility may also vary with the pH of the solution due to ionization states of the amine and carbamate functionalities.

It's important to note that the precise solubility is typically determined through experimental methods, and thus *exact values* can vary. As a rule of thumb, one might say that:

  1. Compounds resembling structures of (isopropylideneamino) N-phenylcarbamate may dissolve better in basic environments.
  2. Careful consideration of functional groups plays a critical role in predicting solubility behavior.

To conclude, understanding the solubility of (isopropylideneamino) N-phenylcarbamate requires an appreciation of its interactions with various solvents, temperature variations, and environmental pH, making it a fascinating subject of study in the realm of chemistry.

Interesting facts

Interesting Facts about (Isopropylideneamino) N-phenylcarbamate

(Isopropylideneamino) N-phenylcarbamate, also known as a type of carbamate, is a compound that holds significance in various fields of chemistry and pharmaceuticals. Here are some key insights into this intriguing compound:

  • Chemical Structure: This compound features a unique isopropylidene group linked to a carbamate moiety, which plays a crucial role in its reactivity. The presence of the N-phenyl group adds aromatic stability and enhances its potential applications.
  • Functional Properties: Carbamates are known for their versatility, making them useful in the synthesis of various agrochemicals and pharmaceuticals. They often exhibit interesting biological activities, which can lead to potential applications in drug design.
  • Synthesis: The synthesis of (isopropylideneamino) N-phenylcarbamate can be achieved through various methods, often involving the reaction of isocyanates with amines. Understanding the synthetic pathways is crucial in organic chemistry, as it highlights the principles of reactivity.
  • Biological Relevance: Several carbamates, including derivatives similar to (isopropylideneamino) N-phenylcarbamate, have shown promise in the development of pharmaceuticals that target neurological disorders and other medical conditions. Their mechanism of action often involves the inhibition of specific enzymes, showcasing their importance in medicinal chemistry.
  • Environmental Impact: It is essential to consider the environmental aspects of carbamates, as they can behave differently in various biological systems. Understanding their degradation pathways helps in evaluating their effect on ecosystems, especially when used as pesticides.

In summary, (isopropylideneamino) N-phenylcarbamate is an intriguing compound that bridges the gap between synthetic organic chemistry and practical applications in pharmaceuticals and agriculture. Its unique structure and versatile properties continue to inspire research and innovation in the field of chemical science.

Synonyms
PROXIMPHAM
Acetone O-carbaniloyloxime
Proxypham
2828-42-4
Proximphan
Acetone oxime phenylurethane
Acetone, O-(phenylcarbamoyl)oxime
O-(N-Phenylcarbamoyl)propanonoxime
O-(N-Phenylcarbamoyl) 2-propanone oxime
O-(N-Phenylcarbamoyl)-propanonoxim
NSC 5607
Acetone, oxime, O-(phenylcarbamate)
NSC 61379
O-(N-Fenylkarbamoyl)propanonoxim
(propan-2-ylideneamino) N-phenylcarbamate
2-Propanone, O-((phenylamino)carbonyl)oxime
2-Propanone, O-[(phenylamino)carbonyl]oxime
43W8J9PAIK
NSC-5607
NSC-61379
(propan-2-ylidene)amino N-phenylcarbamate
Acetone, N-(phenylcarbamate)
Acetone, O-(phenylcarbamate)
Proximpham [German]
Acetone oxime N-phenylcarbamate
Acetone O-(N-phenylcarbamoyl)oxime
EINECS 220-591-0
UNII-43W8J9PAIK
BRN 2211400
O-(N-Fenylkarbamoyl)propanonoxim [Czech]
AI3-23724
O-(N-Phenylcarbamoyl)-propanonoxim [German]
3-12-00-00812 (Beilstein Handbook Reference)
SCHEMBL1674417
acetone O-(anilinocarbonyl)oxime
O-(N-phenylcarbamoyl)propanoxime
DTXSID70182529
NSC5607
NSC61379
Acetone, oxime, N-(phenylcarbamate)
STK367086
AKOS005443912
NS00003440
(phenylamino)[(propan-2-ylideneamino)oxy]methanone
Q27258676
[({[(1-methylethylidene)amino]oxy}carbonyl)amino]benzene
[(([(1-Methylethylidene)amino]oxy)carbonyl)amino]benzene #
CARBAMIC ACID,N-PHENYL,ACETONOXIME ESTER MFC10 H12 N2 O2
InChI=1/C10H12N2O2/c1-8(2)12-14-10(13)11-9-6-4-3-5-7-9/h3-7H,1-2H3,(H,11,13