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Isopentyl 2-[2-(diethylamino)ethylamino]-2-phenylacetate

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Identification
Molecular formula
C18H29NO2
IUPAC name
isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate
State
State

At room temperature, isopentyl 2-[2-(diethylamino)ethylamino]-2-phenylacetate is typically in a liquid state. Its precise state can vary slightly depending on environmental conditions such as its proximity to melting or boiling points.

Melting point (Celsius)
-18.00
Melting point (Kelvin)
255.15
Boiling point (Celsius)
361.10
Boiling point (Kelvin)
634.25
General information
Molecular weight
306.46g/mol
Molar mass
306.4590g/mol
Density
1.0487g/cm3
Appearence

Isopentyl 2-[2-(diethylamino)ethylamino]-2-phenylacetate typically appears as a liquid or an oil. The appearance can vary depending on purity. As a synthesized chemical, it might be slightly viscous with a potential characteristic amine-like odor, due to the diethylamino group present in its structure.

Comment on solubility

Solubility of Isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate (C18H29NO2)

The solubility of isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate can be quite intriguing due to its complex molecular structure. This compound, with its long hydrophobic carbon chain, presents a unique behavior in various solvents.

  • Polar Solvents: Generally, the presence of the amine groups may enhance solubility in polar solvents like water, but the hydrophobic isopentyl group can counteract this.
  • Non-Polar Solvents: Compounds with similar structures are often more soluble in organic solvents such as ethanol and chloroform, where the hydrophobic region can interact more favorably.
  • Temperature Effects: Increased temperature tends to increase the solubility of organic compounds in solvents, suggesting that warming the solvent could improve the dissolution of this acetate.

In summary, while isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate may have some level of solubility in both polar and non-polar solvents, its solubility is ultimately influenced by the balance between its hydrophilic and hydrophobic portions. As the saying goes, "Like dissolves like," and this principle is crucial to understanding the solubility behavior of this compound.

Interesting facts

Interesting Facts about Isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate

This compound, known as isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate, offers a fascinating example of the intersection between organic chemistry and pharmacology. Here are some intriguing points to consider:

  • Structural Complexity: This compound features a complex structure that incorporates both an isopentyl group and a diethylamino moiety. This unique combination often contributes to its diverse biological activities.
  • Pharmacological Relevance: Compounds with similar structures are often investigated for their potential as therapeutic agents. The incorporation of amine groups in the structure can enhance interactions with biological targets, making it a compound of interest in drug design.
  • Potential Applications: Its potential uses might span various fields, including:
    • Pharmaceuticals, particularly in the development of new medications.
    • Research applications focused on molecular biology and pharmacokinetics.
    • Cosmetics, where specific ester compounds are valued for their emollient properties.
  • Reactivity: The presence of both amino and ester functional groups in this compound might play a crucial role in its reactivity. Understanding these interactions is vital for chemists developing new derivatives.
  • Future Research: The ongoing study of such compounds often leads to valuable insights. Research might focus on:
    • Optimizing the pharmacological efficacy.
    • Exploring modifications to enhance stability.
    • Investigating the compound's mechanisms of action in biological systems.

In conclusion, isopentyl 2-[2-(diethylamino)ethylamino]-2-phenyl-acetate is more than just a chemical formula; it embodies the potential for innovation within the realms of organic chemistry and pharmaceuticals. Understanding such compounds can aid in unlocking new therapeutic strategies and addressing medical needs.

Synonyms
Camylofine
Camylofin
54-30-8
Acamylophenine
Navadyl
Adopon
Sintespasmil
Camilofina
Camylopin
Novospasmin
Spasmocan
Avadyl
Avocan
Belosin
Camylofinum
Anafortan
Camylofin [INN:DCF]
Camylofine [INN-French]
Camylofinum [INN-Latin]
Camilofina [INN-Spanish]
Camylofin free base
Camylofine dihydrochloride
3-methylbutyl 2-[2-(diethylamino)ethylamino]-2-phenylacetate
EINECS 200-202-0
Camylofin (INN)
BRN 2816984
DTXSID7046415
UNII-340B6Q764V
CAMYLOFIN [INN]
CAMYLOFINE [MI]
CAMYLOFIN [WHO-DD]
B-Diethylaminoethylaminophenylacetic acid isoamyl ester
N-(2-Diethylaminoethyl)-2-phenylglycine isopentyl ester
Isoamyl N-(beta-diethylaminoethyl)-alpha-aminophenylacetate
N-(2-(Diethylamino)ethyl)-2-phenylglycine, isopentyl ester
Phenyldiethylaminoethyl-1'-aminoacetic acid, isopentyl ester
DTXCID5026415
Acamylophenine hydrochloride
alpha-(N,beta-Diethylaminoethyl)aminophenylacetic acid isoamyl ester
4-14-00-01336 (Beilstein Handbook Reference)
Isopentyl alcohol, ester with N-(2-(diethylamino)ethyl)-2-phenylglycine
Benzeneacetic acid, alpha-(2-(diethylaminoethyl)amino)-, 3-methylbutyl ester
340B6Q764V
NCGC00164526-01
NCGC00164526-02
Camylofine (INN-French)
Camylofinum (INN-Latin)
GLYCINE, N-(2-(DIETHYLAMINO)ETHYL)-2-PHENYL-, ISOPENTYL ESTER
Camilofina (INN-Spanish)
CAS-54-30-8
3-methylbutyl 2-(2-(diethylamino)ethylamino)-2-phenylacetate
Acamylophenine HCl
Anafortan (TN)
N-(2-(Diethylamino)ethyl)phenylglycine isopentyl ester
SCHEMBL617472
CHEMBL253592
CHEBI:95216
A03AA03
HY-B1230
Tox21 112157
Tox21_112157
BDBM50237286
AKOS024386253
Tox21_112157_1
CS-4877
DB13738
DA-51563
SBI-0207043.P001
NS00004488
D07076
AB01563237_01
AB01563237_02
Q4725854
BRD-A91733352-300-03-7
BRD-A91733352-300-04-5
BRD-A91733352-300-05-2
3-Methylbutyl {[2-(diethylamino)ethyl]amino}(phenyl)acetate
3-methyl butyl 2-(2-diethyl amino ethyl amino)-2-phenyl acetate
2-[2-(diethylamino)ethylamino]-2-phenylacetic acid 3-methylbutyl ester
200-202-0