Interesting facts
Interesting Facts about (2S,5R)-2-isopropyl-5-methyl-cyclohexanone
(2S,5R)-2-isopropyl-5-methyl-cyclohexanone is a fascinating compound within the world of organic chemistry. This compound belongs to the family of ketones, which are characterized by the presence of a carbonyl group (C=O) bonded to two carbon atoms. Here are a few compelling points about this intriguing molecule:
- Structural Insight: The stereochemistry of this molecule is of particular interest. The specific configuration of the stereocenters at C-2 and C-5 defines its chirality. The notation S and R indicates the arrangement of substituents in a manner that can have significant implications on its reactivity and interaction with biological molecules.
- Applications: Ketones are crucial in various fields such as pharmaceuticals and flavoring agents. The unique structure of (2S,5R)-2-isopropyl-5-methyl-cyclohexanone makes it a potential candidate for use in fragrance compositions while also being studied for its biological activities.
- Natural Occurrence: Compounds similar in structure often show up in nature. They can be found in essential oils and can impart distinctive aromas to different plants, contributing to ecological interactions.
- Reaction Mechanisms: Beyond its applications, understanding the reaction mechanisms involving (2S,5R)-2-isopropyl-5-methyl-cyclohexanone can provide insights into further synthetic pathways for creating more complex molecules.
- Synthesis Challenge: The synthesis of this specific compound poses interesting challenges in terms of selectivity and yield, making it a subject of study for synthetic chemists aiming for efficiency and effectiveness in reaction design.
To sum up, (2S,5R)-2-isopropyl-5-methyl-cyclohexanone is more than just a simple ketone; it is a compound rich in potential and reactivity that can lead to significant advancements in various scientific fields. As any chemist would say, "It's the small details that can lead to great discoveries!"
Synonyms
MENTHONE
trans-Menthone
p-Menthone
Neomenthone
Menthone racemic
89-80-5
trans-Menthan-3-one
trans-p-Menthan-3-one
p-Menthan-3-one, trans-
Menthone G
(2S,5R)-5-methyl-2-propan-2-ylcyclohexan-1-one
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, trans-
9NH5J4V8FN
CHEBI:36503
SINGLEEX ISOMENTHONE
MENTHONE, (A+-)-
201-941-1
214-049-2
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, (2R,5S)-rel-
(-)-Menthone
14073-97-3
l-MENTHONE
(2S,5R)-2-isopropyl-5-methylcyclohexanone
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, (2S,5R)-
L-Menthan-3-one
DL-Menthone
(1R,4S)-(-)-p-Menthan-3-one
(-)-(2S,5R)-Menthone
FEMA No. 2667
MFCD00001634
(1R,4S)-p-menthan-3-one
(2S,5R)-5-methyl-2-(propan-2-yl)cyclohexanone
(2S,5R)-5-METHYL-2-(1-METHYLETHYL)-CYCLOHEXANONE
(2S,5R)-5-methyl-2-(1-methylethyl)cyclohexanone
(2S-trans)-5-methyl-2-(1-methylethyl)cyclohexanone
(-)-(1R,4S)-menthone
(2S,5R)-2-isopropyl-5-methyl-cyclohexanone
DTXSID3044384
CHEBI:15410
(-)-5-Methyl-2-(1-methylethyl)cyclohexanone
5F709W4OG4
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, (2S-trans)-
Menthone (natural)
DTXCID1024384
p-Menthan-3-one racemic
MFCD00062998
(dl)-Menthone
CAS-14073-97-3
CCRIS 5747
HSDB 1268
(-)-Menthone (contains up to 15% D-Menthone)
p-Menthan-3-one, dl-
EINECS 201-941-1
EINECS 214-049-2
UNII-9NH5J4V8FN
menthon
UNII-5F709W4OG4
AI3-11106
Menthone (Mixture of Diastereomers)
trans-p-menthone
1-menthone
(-)menthone
5-Methyl-2-(1-methylethyl)cyclohexanone, trans-
NCGC00095606-01
Cyclohexan-1-one, 2-isopropyl-5-methyl-, racemic
EINECS 237-926-1
Menthan-3-one, trans
Spectrum_001299
rel-(2R,5S)-2-isopropyl-5-methylcyclohexanone
MENTHONE [FHFI]
SpecPlus_000437
MENTHONE, L-
L-MENTHONE [MI]
Spectrum2_000691
Spectrum3_001272
Spectrum4_001648
Spectrum5_000495
bmse000375
(-)-Menthone (Standard)
(-)-Menthone, 90%
EC 237-926-1
SCHEMBL21709
BSPBio_002864
KBioGR_002115
KBioSS_001779
MENTHONE, (-)-
SPECTRUM300564
DivK1c_006533
SPBio_000841
(1S)-trans-p-menthan-3-one
(-)-MENTHONE [FCC]
(2S,5R)-5-Methyl-2-(Propan-2-Yl)Cyclohexan-1-One
CHEMBL276311
orb1297522
DTXSID2044478
HY-N7916R
KBio1_001477
KBio2_001779
KBio2_004347
KBio2_006915
KBio3_002364
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, trans-(+/-)-
(-)-Menthone, analytical standard
HY-N7916
KAA45814
MSK40039
Tox21_111510
Tox21_302153
CCG-38562
MFCD00136033
MSK014083
AKOS006343213
Tox21_111510_1
FM74368
LMPR0102090004
SDCCGMLS-0066582.P001
2-Isopropyl-5-methylcyclohexanone, trans
NCGC00095606-02
NCGC00178425-01
NCGC00255957-01
1ST40039
AS-17440
SY067260
SY113819
(2S,5R)2-isopropyl-5-methylcyclohexanone
CS-0138798
1-METHYL-4-ISOPROPYLCYCLOHEXAN-3-ONE
C00843
EN300-383879
G66775
(2S,5R)-2-Isopropyl-5-methylcyclohexan-1-one
(2S, 5R)-trans-2-isopropyl-5-methylcyclohexanone
Q424902
SR-05000002387
5-Methyl-2-(1-methylethyl)-(2S,5R)-Cyclohexanone
pound inverted exclamation markA pound(c)-Menthone
SR-05000002387-1
5-Methyl-2-(1-methylethyl)-(2S-trans)-Cyclohexanone
(-)-Menthone, primary pharmaceutical reference standard
rel-(2S,5R)-5-methyl-2-(1-methylethyl)-cyclohexanone
Z1201619246
Cyclohexanone, 5-methyl-2-(1-methylethyl)-, trans-(.+/-.)-
1/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9+/m1/s
InChI=1/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9+/m1/s
Solubility of (2S,5R)-2-isopropyl-5-methyl-cyclohexanone
The solubility of (2S,5R)-2-isopropyl-5-methyl-cyclohexanone can be quite interesting due to its structural characteristics. Being a ketone, solubility in various solvents can vary significantly. Here are some key points to consider:
In summary, while (2S,5R)-2-isopropyl-5-methyl-cyclohexanone shows moderate solubility in polar solvents and better solubility in non-polar solvents, detailed solubility data in specific conditions can provide more precise insights. Understanding these dynamics is essential when handling this compound in various chemical processes.