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Felbamate

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Identification
Molecular formula
C11H14N2O4
CAS number
25451-15-4
IUPAC name
1,1-diphenylprop-2-ynyl N-cyclohexylcarbamate
State
State

Felbamate is a solid at room temperature.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
407.50
Boiling point (Kelvin)
680.65
General information
Molecular weight
238.26g/mol
Molar mass
238.2640g/mol
Density
1.2300g/cm3
Appearence

Felbamate is a white to off-white crystalline powder. It is odorless.

Comment on solubility

Solubility of 1,1-Diphenylprop-2-ynyl N-cyclohexylcarbamate (C11H14N2O4)

1,1-Diphenylprop-2-ynyl N-cyclohexylcarbamate exhibits interesting characteristics regarding its solubility:

  • Polarity: Due to the presence of both hydrophilic (the carbamate group) and hydrophobic (the phenyl groups and cyclohexyl ring) parts in its structure, the solubility can vary significantly.
  • Solvent Compatibility: This compound is likely to be soluble in organic solvents such as dimethyl sulfoxide (DMSO), ethanol, and acetone, owing to its non-polar segments.
  • Aqueous Solubility: Its water solubility might be limited due to large non-polar groups, making it less favorable in polar environments.

When assessing solubility, it’s crucial to consider the solvent's characteristics. As a general principle:

  1. Like dissolves like: Polar solutes are more soluble in polar solvents, while non-polar solutes dissolve better in non-polar solvents.
  2. By understanding the balance of properties in 1,1-diphenylprop-2-ynyl N-cyclohexylcarbamate, one can predict its solubility in different mediums.

In practical terms, for synthesis or application, solubility insights will guide the choice of solvents that facilitate desired reactions or processes.

Interesting facts

Interesting Facts about 1,1-Diphenylprop-2-ynyl N-Cyclohexylcarbamate

The compound 1,1-diphenylprop-2-ynyl N-cyclohexylcarbamate is a fascinating example of a carbamate derivative that showcases the intricate world of organic chemistry. Here are some intriguing aspects of this compound:

  • Structure and Binding: This compound features a uniquely structured backbone composed of a phenyl group and a carbamate moiety, highlighting the structural diversity prevalent in organic compounds.
  • Applications: Compounds like this one may play roles in various fields, including agricultural chemistry, where they can be developed into pesticides or herbicides due to their ability to inhibit certain biological activities.
  • Mechanism of Action: Carbamates are known to interact with enzymes, particularly those involved in neurotransmission, making them important in the study of neurochemistry and toxicology.
  • Synthetic Versatility: The synthesis of carbamate compounds often involves versatile chemistries, allowing chemists to explore innovative synthetic pathways to create related structures.
  • Research Potential: Scientists frequently investigate such compounds to understand their biological interactions better, paving the way for new drug development and other applications in medicinal chemistry.

As one delves deeper into the study of 1,1-diphenylprop-2-ynyl N-cyclohexylcarbamate, it becomes evident that the compound not only illustrates the beauty of chemical synthesis but also holds potential for addressing practical challenges in various scientific domains.

Synonyms
ENPROMATE
10087-89-5
Lilly 59156
1,1-diphenylprop-2-ynyl N-cyclohexylcarbamate
1,1-Diphenyl-2-propynyl cyclohexylcarbamate
Empromate
1,1-Diphenyl-2-propynyl cyclohexanecarbamate
NSC-112682
1,1-Diphenyl-2-propynylcyclophosphamide
1,1-Diphenyl-2-propynyl N-cyclohexylcarbamate
1,1-Diphenyl-2-propynyl-N-cyclohexylcarbamate
Carbamic acid, cyclohexyl-, 1,1-diphenyl-2-propynyl ester
Cyclohexanecarbamic acid, 1,1-diphenyl-2-propynyl ester
HBS2850E4H
NSC112682
1,1-diphenylprop-2-yn-1-yl cyclohexylcarbamate
Empromato [INN-Spanish]
1,1-Diphenyl-2-propynyl cyclohexylcarbamate; NSC 112682
Enpromatum
Empromato
Enpromate [USAN:INN]
Enpromatum [INN-Latin]
Acetylenic carbamate
CCRIS 1009
NSC 112682
BRN 2669373
UNII-HBS2850E4H
Enpromato
2-Propyn-1-ol, 1,1-diphenyl-, cyclohexanecarbamate
ENPROMATE [INN]
Enpromate (USAN/INN)
ENPROMATE [USAN]
SCHEMBL4811
1,1-di(phenyl)prop-2-ynyl N-cyclohexylcarbamate
CHEMBL2106211
DTXSID30143555
CHEBI:177825
WLN: L6TJ AMVOXR&R&1U1
AKOS040751688
1, 1-Diphenyl-2-propynylcyclophosphamide
NS00123674
1, 1-Diphenyl-2-propynyl cyclohexylcarbamate
Carbamic acid, 1,1-diphenyl-2-propynyl ester
D04007
1, 1-Diphenyl-2-propynyl N-cyclohexylcarbamate
1,1-DIPHENYL-2-PROPYNL-CYCLOHEXYL-CARBAMATE
Cyclohexanecarbamic acid,1-diphenyl-2-propynyl ester
Q27279851