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Camphor

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Identification
Molecular formula
C10H16O
CAS number
76-22-2
IUPAC name
1,7,7-trimethylnorbornan-2-one
State
State

Camphor is a solid at room temperature. It easily sublimes and has a distinct aromatic odor.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
152.24g/mol
Molar mass
152.2370g/mol
Density
0.9920g/cm3
Appearence

Camphor is a waxy, flammable, white or transparent solid with a strong aroma. It is granular and crystalline in form and is often used in mothballs.

Comment on solubility

Solubility of 1,7,7-Trimethylnorbornan-2-one

1,7,7-Trimethylnorbornan-2-one (C10H16O) presents intriguing solubility characteristics that can be essential for its applications in both industrial and laboratory settings. The compound's solubility can be influenced by various factors:

  • Polarity: Due to the presence of a carbonyl group (C=O), the molecule exhibits some polar characteristics, enhancing its solubility in polar solvents.
  • Hydrophobic Region: The bulkiness of the trimethyl groups contributes to a hydrophobic region, which can lead to limited solubility in water.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane, which can interact favorably with its structure.

In terms of practical application, it is essential to consider the following:
- Effectiveness in formulations: Its solubility traits could impact its effectiveness as a flavoring or fragrance compound.
- Extraction processes: Knowledge of its solubility behavior is crucial when isolating it from natural sources or synthesizing in lab settings.

In summary, understanding the solubility of 1,7,7-trimethylnorbornan-2-one can provide valuable insights into its behavior in various chemical environments, making it a significant aspect of its chemistry.

Interesting facts

Interesting Facts about 1,7,7-Trimethylnorbornan-2-one

1,7,7-trimethylnorbornan-2-one is an intriguing organic compound belonging to the class of ketones. This compound is particularly noteworthy due to its fascinating structure and potential applications. Here are some interesting aspects:

  • Unique Structure: The compound features a bicyclic norbornane framework combined with a ketone functional group, which gives it unique stereochemical properties and intriguing reactivity.
  • Flavors and Fragrances: Ketones like 1,7,7-trimethylnorbornan-2-one often possess distinctive odors and are found in various flavoring and fragrance applications, making them valuable in the perfume industry. Its structural uniqueness may contribute to creating certain captivating scents.
  • Catalytic Potential: The presence of the ketone functional group provides opportunities for selective reactions in organic synthesis, making this compound a subject of interest for chemists looking to innovate new pathways or synthesize complex molecules.
  • Research Applications: Compounds of this nature have been studied for their biological activity, including potential roles in medicinal chemistry, which opens pathways for drug discovery.

As a chemistry student or enthusiast, delving into the studies surrounding 1,7,7-trimethylnorbornan-2-one can unveil the broader implications of such compounds in industrial applications and organic synthesis. The interplay between structure and function in chemistry is exemplified by such compounds.

In the words of acclaimed chemist Robert H. Grubbs, "To be a scientist, you need to be curious, creative, and resilient." This epitomizes the adventure of exploring the world of organic compounds like 1,7,7-trimethylnorbornan-2-one.

Synonyms
camphor
76-22-2
DL-Camphor
2-Camphanone
(+/-)-Camphor
2-Bornanone
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
Bornan-2-one
21368-68-3
Alphanon
Kampfer
Formosa camphor
Laurel camphor
D-(+)-Camphor
Matricaria camphor
Camphor, synthetic
Bornane, 2-oxo-
1,7,7-Trimethylnorcamphor
Japan camphor
2-Camphonone
Huile de camphre
2-Kamfanon
l-(-)-Camphor
1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone
2-Keto-1,7,7-trimethylnorcamphane
Norcamphor, 1,7,7-trimethyl-
DTXSID5030955
CHEBI:36773
4,7,7-trimethylbicyclo[2.2.1]heptan-3-one
MFCD00074738
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-
Caswell No. 155
SYNTHETIC CAMPHOR
DTXCID3010955
1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone
1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one
Zang Qi
DL-Bornan-2-one
HSDB 37
(-)-Alcanfor
( inverted exclamation markA)-Camphor
Camphor, (1R,4R)-(+)-
Camphor, (+/-)-
EINECS 200-945-0
EINECS 244-350-4
UNII-5TJD82A1ET
EPA Pesticide Chemical Code 015602
BRN 1907611
BRN 3196099
AI3-18783
(1RS,4RS)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-one
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-
Camphor (USP)
EC 200-945-0
0-07-00-00135 (Beilstein Handbook Reference)
4-07-00-00213 (Beilstein Handbook Reference)
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-
racemic camphor
NSC26351
MFCD00064149
Camphor, natural
DL-2-Bornanone
()-Camphor
Heet (Salt/Mix)
Camphor (Standard)
Sarna (Salt/Mix)
(?)-Camphor
dl-Camphor (JP17)
(.+/-.)-Camphor
SCHEMBL16068
Camphor, (.+/-.)-
MLS001055495
CHEMBL15768
DivK1c_000724
GTPL2422
HMS502E06
HY-N0808R
KBio1_000724
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-
NINDS_000724
HMS2268A06
HMS3885J06
HY-N0808
Tox21_200237
BBL012963
s3851
s4516
STK803534
AKOS000118728
AKOS022060577
AC-5284
CCG-266237
CCG-266238
DB14156
FC31875
LMPR0102120001
UN 2717
CAS-76-22-2
IDI1_000724
USEPA/OPP Pesticide Code: 015602
NCGC00090681-05
NCGC00090730-01
NCGC00090730-02
NCGC00090730-05
NCGC00257791-01
1ST40229
AC-15523
SMR000386909
SY025804
SY035827
VS-03622
(1R,4R)-1,7,7-trimethylnorbornan-2-one
DB-051377
DB-056037
DB-070734
C1251
CS-0009813
NS00003762
4,7,7-trimethyl-3-bicyclo[2.2.1]heptanone
EN300-19186
1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-one
C18369
D00098
E75814
1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-one
A838646
Q181559
(+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one
F0001-0763
Z104473074
200-945-0