Interesting facts
Interesting Facts about Cyclohex-3-ene-1-carbaldehyde
Cyclohex-3-ene-1-carbaldehyde is a fascinating compound in the world of organic chemistry, known for its unique structure and reactivity. Here are some interesting points to consider:
- Structure: This compound features a cyclohexene ring, which provides a degree of unsaturation and reactivity not found in fully saturated aliphatic aldehydes. The presence of the aldehyde functional group at the 1 position offers intriguing possibilities for chemical transformations.
- Reactivity: Due to its unsaturation, cyclohex-3-ene-1-carbaldehyde can undergo various reactions, such as cycloadditions and nucleophilic additions, making it a valuable intermediate in organic synthesis.
- Synthetic Utility: The compound serves as a building block in the synthesis of more complex organic molecules. Its versatility is particularly notable in the pharmaceutical industry for developing potential drug candidates.
- Chemical Behavior: As an aldehyde, it can readily participate in condensation reactions, which can affect its reactivity in different chemical environments.
- Flavor and Fragrance: Compounds similar in structure often have applications in the flavor and fragrance industries. Their structure may influence olfactory properties, contributing to fragrance formulations.
As noted chemist Robert H. Grubbs once said, "The beauty of chemistry lies in its ability to weave simple elements into intricate tapestries of compounds." Cyclohex-3-ene-1-carbaldehyde is a perfect example of this elegance, representing the intersection of simplicity and complexity in organic synthesis.
In conclusion, cyclohex-3-ene-1-carbaldehyde not only captivates chemists with its structural features but also paves the way for advancements in organic synthesis, highlighting the profound impact of such compounds in the broader scientific community.
Synonyms
3-CYCLOHEXENE-1-CARBOXALDEHYDE
100-50-5
Cyclohex-3-ene-1-carbaldehyde
1,2,3,6-Tetrahydrobenzaldehyde
4-Formylcyclohexene
Cyclohexene-4-carboxaldehyde
1-Formyl-3-cyclohexene
1-Cyclohexene-4-carboxaldehyde
1,2,5,6-Tetrahydrobenzaldehyde
3-Cyclohexen-1-aldehyde
4-Cyclohexene-1-carboxaldehyde
delta1-Tetrahydrobenzaldehyde
3-Cyclohexene-1-carbaldehyde
NSC 16241
4-Formyl-1-cyclohexene
HSDB 5334
cyclohex-3-enecarbaldehyde
EINECS 202-858-3
UN2498
BRN 0774001
DTXSID1026661
AI3-21661
NSC-16241
GAK9539347
DTXCID006661
EC 202-858-3
4-07-00-00134 (Beilstein Handbook Reference)
.DELTA.1-TETRAHYDROBENZALDEHYDE
.DELTA.3-TETRAHYDROBENZALDEHYDE
3-CYCLOHEXEN-1-ALDEHYDE [HSDB]
3-CYCLOHEXENE-1-CARBOXALDEHYDE, (+/-)-
Benzaldehyde, tetrahydro-
UNII-GAK9539347
4Formylcyclohexene
1Formyl3cyclohexene
EINECS 215-315-0
3Cyclohexen1aldehyde
MFCD00001572
3-cyclohexenecarbaldehyde
Cyclohex3ene1carbaldehyde
Cyclohexene4carboxaldehyde
WLN: L6UTJ DVH
3-cyclohexenecarboxaldehyde
1,2,3,6-Tetrahydrobenzaldehyde(1,2,5,6)
1Cyclohexene4carboxaldehyde
4Cyclohexene1carboxaldehyde
delta1Tetrahydrobenzaldehyde
3-cyclohexene carboxaldehyde
SCHEMBL42869
1,3,6-Tetrahydrobenzaldehyde
1,5,6-Tetrahydrobenzaldehyde
3-cyclohexene-1-carboaldehyde
1,2,3,6tetrahydrobenzaldehyde
1,2,5,6tetrahydrobenzaldehyde
1,2,3,6-tetrahydrobenzaldehyd
3-Cyclohexene-1-carbaldehyde #
CHEMBL3188123
DELTA3-TETRAHYDROBENZALDEHYDE
NSC16241
STR03930
Tox21_201059
STK397283
DELTA 1-TETRAHYDROBENZALDEHYDE
3-Cyclohexene-1-carboxaldehyde, 97%
AKOS000119878
AKOS016843227
UN 2498
NCGC00248910-01
NCGC00258612-01
CAS-100-50-5
FC170544
NS00002610
(+-)-3-CYCLOHEXENE-1-CARBOXALDEHYDE
EN300-18427
A18008
(.+-.)-3-CYCLOHEXENE-1-CARBOXALDEHYDE
Q27278997
Z57936862
F8889-7486
cyclohex-3-enecarbaldehyde;3-Cyclohexene-1-carboxaldehyde
1,2,3,6-Tetrahydrobenzaldehyde [UN2498] [Flammable liquid]
202-858-3
Solubility of Cyclohex-3-ene-1-carbaldehyde
Cyclohex-3-ene-1-carbaldehyde, a compound with a unique structure, exhibits interesting solubility characteristics that are worth noting:
In summary: The solubility of cyclohex-3-ene-1-carbaldehyde is influenced by its structural features, aligning with the common principle that “like dissolves like.” Thus, it is best soluble in organic solvents where it can interact effectively, while remaining largely insoluble in water.