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Surrogates

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Identification
Molecular formula
C13H21NO2
CAS number
40054-69-1
IUPAC name
(1-prop-2-ynylcyclohexyl) carbamate
State
State

At room temperature, (1-prop-2-ynylcyclohexyl) carbamate is typically found as a liquid. It is important to handle with care due to its chemical reactivity, and standard laboratory precautions should be followed during its handling and storage.

Melting point (Celsius)
5.00
Melting point (Kelvin)
278.10
Boiling point (Celsius)
282.50
Boiling point (Kelvin)
555.70
General information
Molecular weight
225.32g/mol
Molar mass
225.2870g/mol
Density
1.0750g/cm3
Appearence

(1-prop-2-ynylcyclohexyl) carbamate is generally a clear, colorless to pale yellow liquid. It may appear as a crystalline solid under certain conditions, but typically, it maintains a liquid state at room temperature. The compound is used mainly in chemical synthesis and research, and it does not have a prominent color or any distinctive features aside from its basic liquid appearance.

Comment on solubility

Solubility of (1-prop-2-ynylcyclohexyl) carbamate

The solubility of (1-prop-2-ynylcyclohexyl) carbamate in various solvents is an intriguing aspect of this compound's chemistry. Generally, solubility can vary greatly depending on several factors:

  • Polarity of the solvent: This compound, being a carbamate, is likely to exhibit moderate solubility in polar solvents like water due to its potential hydrogen bonding capability.
  • Temperature: Increased temperatures often improve solubility for organic compounds; therefore, heating a solution may enhance the dissolution of (1-prop-2-ynylcyclohexyl) carbamate.
  • Functional groups: The presence of a carbamate group typically suggests that this compound can interact favorably with other polar functional groups, which may aid its solubility in organic solvents.
  • pH levels: The solubility may also be influenced by the pH of the solution, as protonation or deprotonation of the carbamate group could change its solubility profile.

It is often observed that compounds with aliphatic chains can vary in solubility based on their length and branching. Therefore, empirical testing is advised to determine the exact solubility behavior of (1-prop-2-ynylcyclohexyl) carbamate in specific scenarios.

To sum up, while the solubility of (1-prop-2-ynylcyclohexyl) carbamate may show promise in polar solvents, further investigation and analysis are essential to fully understand its solubility characteristics:

  • Conduct experiments to determine solubility in various solvents.
  • Examine the impact of temperature and pH on solubility.
Interesting facts

Interesting Facts about (1-prop-2-ynylcyclohexyl) carbamate

(1-prop-2-ynylcyclohexyl) carbamate is a fascinating compound that exemplifies the intricate interplay between structure and function in organic chemistry. Here are some highlights that showcase its significance:

  • Unique Functional Group: This compound contains a carbamate functional group, which is pivotal in various biological activities. Carbamates are well-known for their role in pharmaceutical developments, especially as potential therapeutic agents.
  • Synthetic Applications: (1-prop-2-ynylcyclohexyl) carbamate is often utilized in synthetic organic chemistry. Its distinctive structure can serve as a precursor or building block in the synthesis of more complex molecules.
  • Biological Activity: Compounds featuring the cyclohexyl structure have shown promise in medicinal chemistry. Research into (1-prop-2-ynylcyclohexyl) carbamate may reveal insights into its behavior in biological systems, potentially leading to applications in drug design.
  • Versatile Reactivity: The presence of a triple bond (alkyne) in its structure adds to the compound's reactivity, making it a candidate for various chemical transformations. This reactivity allows for further modifications that can enhance its properties and functionalities.
  • Environmental Considerations: Carbamates are also studied in the context of environmental science. Understanding the degradation pathways and ecological impact of compounds like (1-prop-2-ynylcyclohexyl) carbamate can contribute to safer chemical practices.

In summary, (1-prop-2-ynylcyclohexyl) carbamate is not just a chemical entity; it represents various themes in organic synthesis, medicinal chemistry, and environmental science. The exploration of this compound opens the door for innovative research and applications, bridging gaps between chemistry and real-world challenges.

Synonyms
Hexapropymate
358-52-1
Merinax
Hexopropynate
Modirax
Esapropimato
Lunamin
Hexapropimato
Hexapropymatum
Propynylcyclohexanol carbamate
1-(prop-2-yn-1-yl)cyclohexyl carbamate
Hexapropymate [INN:BAN:DCF]
LF 62
Hexapropymatum [INN-Latin]
1-(2-Propynyl)-1-cyclohexanol carbamate
1-(2-Propynyl)cyclohexyl carbamate
Hexapropimato [INN-Spanish]
1-(2-Propynyl)cyclohexanol carbamate
1-Carbamoyloxy-1-(2-propynyl)cyclohexane
EINECS 206-618-9
(1-prop-2-ynylcyclohexyl) carbamate
0J9RN2PRJ7
Merinax (TN)
L 2103
NSC 169094
NSC-169094
BRN 3253991
Hexapropymate (INN)
Carbamate du propinylcyclohexanol
Carbamate du propinylcyclohexanol [French]
Cyclohexanol, 1-(2-propynyl)-, carbamate
CARBAMIC ACID, 1-(2-PROPYNYL)CYCLOHEXYL ESTER
L-2103
HEXAPROPYMATE [MI]
HEXAPROPYMATE [INN]
HEXAPROPYMATE [MART.]
HEXAPROPYMATE [WHO-DD]
DTXSID00189329
4-06-00-00362 (Beilstein Handbook Reference)
Lunamin; L2103; NSC 169094
Hexapropymatum (INN-Latin)
Hexapropimato (INN-Spanish)
HEXAPROPYMATE (MART.)
UNII-0J9RN2PRJ7
Cyclohexanol, 1-(2-propynyl)-, carbamate (8CI)
SCHEMBL1550506
CHEMBL2104292
WLN: L6TJ AOVZ A2UU1
DTXCID80111820
N05CM10
CHEBI:134823
MIRHIEAGDGUXKL-UHFFFAOYSA-N
AAA35852
NSC169094
AKOS006240457
DB13662
DB-048881
L2103
NS00029933
D07331
EN300-1266505
Q1036070
Cyclohexanol, 1-(2-propynyl)-, carbamate (8CI)(9CI)
Z995241878
206-618-9