Interesting facts
Exploring 4-[1-Hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol
4-[1-Hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol is a fascinating compound with a complex structure that showcases the elegance of organic chemistry. Below are some intriguing aspects of this compound:
- Structural Complexity: This molecule features a benzene ring substituted with hydroxyl groups and an aminoalkyl chain, highlighting its potential for diverse interactions.
- Potential Applications: Due to its structural properties, the compound is of interest in medicinal chemistry, particularly for its role in the development of pharmacologically active compounds.
- Biological Relevance: The presence of the isopropylamino group suggests possible biological activity, making it a candidate for further investigation in biochemical research.
- Research Interest: Scientists are intrigued by the potential of similar compounds to act as enzyme inhibitors, which can lead to novel therapies in various medical fields.
- Synthesis Pathways: Understanding how to synthesize such compounds efficiently opens doors for innovations in synthetic organic chemistry.
In the realm of chemistry, every compound tells a story, and 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol is no exception. Not only does it present opportunities for scientific advancement, but it also serves as a testament to the intricate connection between structure and function in chemical compounds.
Synonyms
isoproterenol
Isoprenaline
7683-59-2
Isopropydrin
Novodrin
Asiprenol
Assiprenol
Bellasthman
Isoprenalin
Respifral
Aludrine
Asmalar
Norisodrine
Neodrenal
Proternol
neo-Epinine
Isopropylarterenol
Isonorin
Saventrine
Isonorene
Aludrin
Isadrine
Isorenin
Lomupren
N-Isopropylnoradrenaline
Isopropyladrenaline
Isopropylnorepinephrine
N-Isopropylnorepinephrine
Bronkephrine
Isupren
Vapo-N-iso
Isopropylnoradrenaline
Isopropyl noradrenaline
dl-Isadrine
Racemic isoprenaline
Racemic isoproterenol
(+-)-Isoproterenol
DL-ISOPROTERENOL
Isoprenalina
Isoprenalinum
Isoproterenolum
Epinephrine isopropyl homolog
(+-)-Isoprenaline
Aleudrin
Aleudrine
4-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzene-1,2-diol
DL(+-)-Isoproterenol
Dihydroxyphenylethanolisopropylamine
WIN 5162
1-(3,4-Dihydroxyphenyl)-2-(isopropylamino)ethanol
ICI 46399
Isoprenalinum [INN-Latin]
Isoprenalina [INN-Spanish]
1-(3,4-Dihydroxyphenyl)-2-isopropylaminoethanol
149-53-1
alpha-(Isopropylaminomethyl)protocatechuyl alcohol
CCRIS 3081
1,2-Benzenediol, 4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-
N-Isopropyl-beta-dihydroxyphenyl-beta-hydroxyethylamine
4-(1-Hydroxy-2-((1-methylethyl)amino)ethyl)-1,2-benzenediol
NSC 9975
NSC-9975
1,2-Benzenediol, 4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)-
Isoproterenol Chloride
EINECS 231-687-7
NSC 33791
NSC-33791
UNII-L628TT009W
BRN 2213857
Isoprenaline (INN)
Isoprenaline [INN]
Isopropylaminomethyl-3,4-dihydroxyphenyl carbinol
Isoproterenol dl-form
DTXSID4023175
CHEBI:64317
L628TT009W
4-(1-Hydroxy-2-(isopropylamino)ethyl)benzene-1,2-diol
3,4-Dihydroxy-alpha-((isopropylamino)methyl)benzyl alcohol
CHEMBL434
Protocatechuyl alcohol, alpha-(isopropylaminomethyl)-
DTXCID603175
Isopropylaminomethyl(3,4-dihydroxyphenyl)carbinol
7683-59-2 (free)
3-13-00-02387 (Beilstein Handbook Reference)
NSC33791
3,4-dihydroxy-alpha-[(isopropylamino)methyl]benzyl alcohol
NCGC00015558-06
3,4-Dihydroxy-.alpha.-(isopropylaminomethyl)-benzyl alcohol
A-21
Isoproterenol [JAN]
Benzyl alcohol, 3,4-dihydroxy-alpha-((isopropylamino)methyl)-
Protocatechuyl alcohol,-
Isoprenalinum (INN-Latin)
Isoprenalina (INN-Spanish)
ISOPRENALINE (MART.)
ISOPRENALINE [MART.]
.alpha.-(Isopropylaminomoethyl)protocatechuyl alcohol
WLN: QR BQ DYQ1MY1&1
3,4-Dihydroxy-.alpha.-[(isopropylamino)methyl]benzyl alcohol
4-{1-hydroxy-2-[(1-methylethyl)amino]ethyl}benzene-1,2-diol
CAS-7683-59-2
ISOPROP
Noradrenaline, Isopropyl
1, 4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-
4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol
4-(1-hydroxy-2-(propan-2-ylamino)ethyl)benzene-1,2-diol
Benzyl alcohol,4-dihydroxy-.alpha.-[(isopropylamino)methyl]-
Isoproterenol-l
3,4-DIHYDROXY-.ALPHA.-((ISOPROPYLAMINO)METHYL)BENZYL ALCOHOL
Isoproterenol (-)
Isoproterenol,(+)
ISOPROTERONOL
Isuprel (Salt/Mix)
Izadrin (Salt/Mix)
Euspiran (Salt/Mix)
L-Isoproterenol; Levisoprenaline; Proternol L
(+/-)-isoprenaline
(+/-)-isoproterenol
Spectrum_000949
Prestwick0_001097
Prestwick1_001097
Prestwick2_001097
Spectrum2_001061
Spectrum3_000474
Spectrum4_000024
Spectrum5_000880
(.+/-.)-Isoprenaline
ISOPROTERENOL [MI]
(.+/-.)-Isoproterenol
SCHEMBL4165
DL(.+/-.)-Isoproterenol
Lopac0_000711
Oprea1_009434
BSPBio_002208
GTPL536
ISOPROTERENOL [VANDF]
KBioGR_000427
KBioSS_001429
DivK1c_000894
ISOPRENALINE [WHO-DD]
SPBio_001042
SPBio_003057
SGCUT00015
4-(1-Hydroxy-2(isopropylamino)ethyl)-benzene 1,2-diol
BDBM25392
KBio1_000894
KBio2_001429
KBio2_003997
KBio2_006565
KBio3_001428
C01CA02
NSC9975
R03AB02
R03CB01
NINDS_000894
4-{1-hydroxy-2-[(propan-2-yl)amino]ethyl}benzene-1,2-diol
HMS2089A12
HMS3742A11
ISOPROTERENOL DL-FORM [MI]
BCP09043
to_000062
(A+/-)-Isoproterenol hydrochloride
Tox21_110172
PDSP1_001425
PDSP2_001409
STL558077
AKOS015913894
Tox21_110172_1
CCG-204727
CCG-204796
DB01064
SDCCGSBI-0050620.P003
SDCCGSBI-0050689.P005
IDI1_000894
NCGC00015558-04
NCGC00015558-05
NCGC00015558-07
NCGC00015558-08
NCGC00015558-09
NCGC00015558-10
NCGC00015558-11
NCGC00015558-12
NCGC00015558-13
NCGC00015558-14
NCGC00015558-25
NCGC00016665-02
NCGC00025274-03
NCGC00025274-04
NCGC00162220-01
114-45-4
TS-08150
SBI-0050689.P004
HY-108353
CS-0028436
NS00001320
C07056
D08090
EN300-148243
AB00053487-09
AB00053487-10
AB00053487_11
AB00053487_12
AG-219/03618046
L000936
Q415550
.alpha.-(Isopropylaminomethyl)protocatechuyl alcohol
BRD-A04322457-003-15-3
BRD-A04322457-003-16-1
BRD-A04322457-003-17-9
BRD-A04322457-003-18-7
4-[1-Hydroxy-2-(isopropylamino)ethyl]-1,2-benzenediol
Protocatechuyl alcohol,.alpha.-(isopropylamino-methyl),-
4-[1-Hydroxy-2-(isopropylamino)ethyl]-1,2-benzenediol #
N-Isopropyl-.beta.-dihydroxyphenyl-.beta.-hydroxyethylamine
4-[1-hydroxy-2-(isopropylamino)ethyl]pyrocatechol;hydrochloride
4-{1-hydroxy-2-[(propan-2-yl)amino]ethyl}benzene-1,2-diol, 2
Benzyl alcohol, 3,4-dihydroxy-.alpha.-((isopropylamino)methyl)-
231-687-7
Solubility of 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol
The solubility of the compound 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol (C8H11NO3) is influenced by several factors, primarily its polar functional groups and hydrophobic aromatic structure. Here are some key considerations regarding its solubility:
It is critical to note that while the compound may dissolve to some extent in water due to its polar functional groups, the extent of solubility can be significantly affected by temperature and the presence of other solutes. In many cases, solubility behavior can vary markedly depending on the solvent used, making experimentation essential to precisely determine its solubility profile.
In conclusion, the solubility of C8H11NO3 presents an interesting interplay between its polar and non-polar characteristics. Further analysis and experimental data will provide a clearer picture of its solubility in various conditions.