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Tetralin-5-yl N-methylcarbamate

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Identification
Molecular formula
C12H15NO2
CAS number
22063-27-0
IUPAC name
tetralin-5-yl N-methylcarbamate
State
State

Tetralin-5-yl N-methylcarbamate is typically found as a solid at room temperature, often in a crystalline form.

Melting point (Celsius)
43.00
Melting point (Kelvin)
316.15
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.15
General information
Molecular weight
207.25g/mol
Molar mass
207.2530g/mol
Density
1.1500g/cm3
Appearence

Tetralin-5-yl N-methylcarbamate is a solid compound with a crystalline appearance. It is typically odorless and has a white to off-white color.

Comment on solubility

Solubility of Tetralin-5-yl N-methylcarbamate

Tetralin-5-yl N-methylcarbamate, a compound derived from the fusion of tetralin and carbamate functionalities, exhibits unique solubility properties that are quite intriguing. Understanding its solubility can provide insights into its reactivity and potential applications.

The solubility of tetralin-5-yl N-methylcarbamate can be influenced by several factors:

  • Polarity: The presence of both the tetralin (a relatively nonpolar aromatic hydrocarbon) and the carbamate functional group (which is polar) suggests that this compound can have differing solubility behaviors in various solvents.
  • Solvent Interactions: It is likely to be soluble in polar organic solvents such as methanol, ethanol, and acetone, while showing reduced solubility in nonpolar solvents like hexane or toluene.
  • Temperature Effects: As with many organic compounds, an increase in temperature can enhance solubility, promoting better dissolution in cases where solid phase exists.
  • Hydrogen Bonding: The ability of the carbamate group to form hydrogen bonds could also facilitate solubility in protic solvents, emphasizing the role of interactions with solvent molecules.

In summary, "the solubility of tetralin-5-yl N-methylcarbamate is dictated by its structural features and the nature of the solvent used." This compound demonstrates that solubility is not just a matter of 'like dissolving like', but also a complex interplay of molecular interactions that can lead to diverse behaviors in different environments.

Interesting facts

Exploring Tetralin-5-yl N-methylcarbamate

Tetralin-5-yl N-methylcarbamate is a fascinating compound situated at the intersection of organic chemistry and application in various scientific fields. Below are some captivating facts about this compound:

  • Structural Interest: The compound features a unique structure derived from tetralin, which is a bicyclic hydrocarbon. This aspect provides it with interesting chemical reactivity and potential applications in synthesis.
  • Biological Relevance: Carbamates, such as N-methylcarbamate, are known for their biological activity. They can act as inhibitors in enzymatic reactions, making them significant in studies related to pharmaceuticals and pest control.
  • Practical Applications: Tetralin-5-yl N-methylcarbamate may have potential applications in agriculture as a pesticide or herbicide, capitalizing on the carbamate group’s activity against various pests.
  • Research Interest: Scientists often investigate compounds like this one for their environmental impact and persistence. Understanding their breakdown and interaction in natural systems can inform safety and regulatory guidelines.
  • Safety Considerations: While studying compounds of this nature, it is essential to consider toxicity and the ecological footprint. Such considerations are critical in evaluating the sustainable use of chemical compounds.

In conclusion, tetralin-5-yl N-methylcarbamate is not just another compound; it embodies the complexity of chemical science and its relevance to both industrial applications and environmental stewardship. As researchers continue to explore its properties and effects, this compound will undoubtedly reveal more of its intriguing secrets.

Synonyms
5,6,7,8-Tetrahydro-1-naphthyl methylcarbamate
5,6,7,8-tetrahydronaphthalen-1-yl N-methylcarbamate
B7P9AX9RG3
CARBAMIC ACID, METHYL-, 1-(5,6,7,8-TETRAHYDRO)NAPHTHYL ESTER
DTXSID3041534
Tetrahydro naphthyl methyl carbamate
TETRAHYDRO-1-NAPHTHYL METHYLCARBAMATE, 5,6,7,8-
1-NAPHTHALENOL, 5,6,7,8-TETRAHYDRO-, 1-(N-METHYLCARBAMATE)
DTXCID1021534
5,6,7,8-Tetrahydro-1-naphthalenyl methylcarbamate
5,6,7,8-Tetrahydro-1-naphthyl methylcarbamic acid
1136-84-1
1-Naphthalenol, 5,6,7,8-tetrahydro-, methylcarbamate
Mam-Tox
Caswell No. 841A
N-Methylcarbamic acid 5,6,7,8-tetrahydronaphthalen-1-yl ester
Union carbide UC-8454
ENT 27253
EPA Pesticide Chemical Code 441200
BRN 1877689
UC 8,454
AI3-27253
5,6,7,8-Tetrahydro-1-naftyl-N-methylkarbamat [Czech]
5,6,7,8-Tetrahydro-1-naftylester kyseliny methylkarbaminove [Czech]
UNII-B7P9AX9RG3
5,6,7,8-Tetrahydro-1-naftyl-N-methylkarbamat
SCHEMBL1872704
FDHRBCMXYSGNPA-UHFFFAOYSA-N
5,6,7,8-Tetrahydro-1-naftylester kyseliny methylkarbaminove
NS00121263
5,6,7,8-Tetrahydro-1-naphthalenyl methylcarbamate #