Interesting facts
Interesting Facts about (1R,2S)-2-(Methylamino)-1-phenyl-propan-1-ol
(1R,2S)-2-(Methylamino)-1-phenyl-propan-1-ol is a notable compound in the field of organic chemistry due to its unique structural features and potential applications.
Key Characteristics
- Stereochemistry: The compound features specific chirality, denoted as (1R,2S), which is critical in medicinal chemistry. Chirality can greatly influence the biological activity of a compound, making this aspect essential for drug design.
- Functional Groups: This compound contains both an amino group and a hydroxyl group, indicating that it can participate in various chemical reactions, making it a versatile compound for synthesis.
- Amine Activity: As a molecule with a methylamino group, it can exhibit interactions typical of amines, such as hydrogen bonding capabilities, which can affect its solubility and reactivity.
Potential Applications
This compound has potential applications in the following areas:
- Pharmaceutical Development: Due to its structural resemblance to biologically active compounds, it can be investigated for potential therapeutic effects.
- Research Studies: The study of such compounds may provide insight into the mechanisms of action of similar molecules in biological systems.
- Drug Formulation: Its characteristics may be useful in formulating drugs that target specific receptors in the body.
Quote from the Field
As researchers often say, "The structure dictates the function." Understanding the nuances of compounds like (1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol helps chemists tailor molecules for desired effects in drug development.
In conclusion, (1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol is more than just a chemical entity; it embodies the intricate relationship between structure, activity, and potential applications in medicinal chemistry.
Synonyms
Ephedrine
l-Ephedrine
(-)-Ephedrine
299-42-3
Ephedrin
L(-)-Ephedrine
Lexofedrin
Ephedrol
Mandrin
Sanedrine
Fedrin
I-Sedrin
1-Sedrin
Ephedrine l-form
(1R,2S)-2-(methylamino)-1-phenylpropan-1-ol
Xenadrine
Norephedrine, N-methyl-
Ephedrine, anhydrous
racephedrine
Ephedrital
Ephedrosan
Ephedrotal
Ephedsol
Ephendronal
Ephoxamin
Kratedyn
Manadrin
Vencipon
Efedrin
Zephrol
Nasol
Ephedrine, L-(-)-
HSDB 3072
l-2-Methylamino-1-phenylpropanol
l-alpha-(1-Methylaminoethyl)benzyl alcohol
NSC 8971
EINECS 206-080-5
UNII-GN83C131XS
l-Erythro-2-(methylamino)-1-phenylpropan-1-ol
NSC 170951
Ephedrinum, anhydrous
GN83C131XS
CHEBI:15407
AI3-02761
(-)-alpha-(1-Methylaminoethyl)benzyl alcohol
NSC-8971
NSC-170951
(1R,2S)-1-phenyl-1-hydroxy-2-methylaminopropane
Biophedrin
Ephedremal
DTXSID0022985
Eciphin
Ephedral
(1R,2S)-2-methylamino-1-phenylpropan-1-ol
Benzenemethanol, alpha-(1-(methylamino)ethyl)-, (R-(R*,S*))-
EC 206-080-5
(1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol
Benzenemethanol, alpha-(1-(methylamino)ethyl)-, (-)-
Sal-Phedrine
EPHEDRINE (MART.)
EPHEDRINE [MART.]
Ephedrine [USAN:BAN]
1-Hydroxy-2-methylamino-1-phenylpropane
(1R,2S)-(-)-ephedrine
EPHEDRINE (EP MONOGRAPH)
EPHEDRINE [EP MONOGRAPH]
EPHEDRINE (USP MONOGRAPH)
EPHEDRINE [USP MONOGRAPH]
(-)-Ephedrine hemisulfate
NSC8971
(L)-EPHEDRINE
(-)-(1R,2S)-Ephedrine
Ephedrine (TN)
Ephedrine (USP)
1-2-Methylamino-1-phenylpropanol
Ephedrine Erythro Isomer
2-Methylamino-1-phenyl-1-propanol
Erythro Isomer of Ephedrine
1-Phenyl-1-hydroxy-2-methylaminopropane
Efedrina
alpha-Hydroxy-beta-methylaminopropylbenzene
1-alpha-(1-Methylaminoethyl)benzyl alcohol
alpha-(1-(Methylamino)ethyl)benzenemethanol
NSC170951
alpha-Hydroxy-beta-methyl amine propylbenzene
1(-)ephedrine
EPHEDRINE [MI]
EPHEDRINE [HSDB]
EPHEDRINE [VANDF]
(1R,2S)-2-methylamino-1-phenyl-propan-1-ol
EPHEDRINE [WHO-DD]
SCHEMBL4785
Lopac0_000501
GTPL556
(1r, 2s)-(-)-ephedrine
CHEMBL211456
DTXCID402985
-(1R,2S)-(-)-ephedrine
Benzenemethanol, alpha-((1S)-1-(methylamino)ethyl)-, (alphaR)-
HY-B1195
Benzenemethanol, .alpha.-[(1S)-1-(methylamino)ethyl]-, (.alpha.R)-
PDSP2_001327
PDSP2_001330
(1R,2S)-(-)-Ephedrine, 98%
AKOS016011257
Emerphed (ephedrine sulfate injection)
EPHEDRINE, ANHYDROUS [WHO-IP]
CCG-204592
CS-4802
DB01364
NCGC00162174-01
NCGC00162174-02
SBI-0051362.P003
EPHEDRINUM, ANHYDROUS [WHO-IP LATIN]
NS00000382
(1R,2S)-2-Methylamino-1-phenyl-1-propanol
C01575
D00124
(1R*,2S*)-2-methylamino-1-phenyl-1-propanol
(1R,2S)-2-(methylamino)-1-phenyl-1-propanol
AB00375843_06
A820118
Q219626
SR-01000075166
(1R,2S)-(-)-2-Methylamino-1-phenyl-1-propanol
SR-01000075166-1
BRD-K45014108-003-01-8
(1R,2S)-(-)-2-(N-methylamino)-1-phenylpropan-1-ol
(1R,2S)-(-)-alpha-(1-Methylaminoethyl)benzenemethanol
(R-(R*,S*))-alpha-(1-(Methylamino)ethyl)benzenemethanol
benzene, 1-hydroxy-2-methylamino)propyl- (-((-) ephedrine)-
PSEUDOEPHEDRINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
BENZENEMETHANOL, .ALPHA.-(1-(METHYLAMINO)ETHYL)-, (R-(R*,S*))-
(R-(R*,S*))-.ALPHA.-(1-(METHYLAMINO)ETHYL)BENZENEMETHANOL [WHO-IP]
206-080-5
Solubility of (1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol
(1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol, a compound characterized by its unique amine structure, exhibits noteworthy solubility characteristics. Its ability to dissolve in various solvents can be influenced by several factors, including:
It is crucial to note:
In summary, the solubility of (1R,2S)-2-(methylamino)-1-phenyl-propan-1-ol is highly dependent on the conditions, particularly the solvent type and temperature. As a general guideline, one might say: "The more polar the environment, the greater the dissolving power." This compound's versatility in solubility makes it a subject of interest in chemical and pharmaceutical applications.