Interesting facts
Interesting Facts About [2-(phenylcarbamoyloxy)-3-(1-piperidyl)propyl] N-phenylcarbamate;hydrochloride
This compound is an intriguing member of the carbamate family, known for its diverse applications in both the pharmaceutical and agricultural sectors. As a hydrochloride salt, it is often studied due to its enhanced stability and solubility in aqueous solutions. Here are some interesting aspects of this compound:
- Pharmaceutical Relevance: This compound exhibits potential as a therapeutic agent. Its structure suggests it could interact with certain biological pathways, which warrants further investigation in drug discovery processes.
- Mechanism of Action: Carbamate derivatives are known to act as inhibitors of acetylcholinesterase. This feature could make the compound useful in treating cognitive disorders by enhancing cholinergic activity in the brain.
- Hybrid Nature: The presence of both a piperidyl and phenyl carbamate moiety in its structure reflects its hybrid nature, combining properties of nitrogen-containing heterocycles with carbamate functionalities. This unique arrangement may contribute to complex pharmacological profiles.
- Potential in Research: The compound could serve as a valuable research tool in neuropharmacology, allowing scientists to explore the effects of carbamates on neurological functions.
- Synergistic Effects: Studies may reveal that combining this compound with other therapeutic agents could yield synergistic effects, enhancing therapeutic outcomes and minimizing side effects.
In summary, [2-(phenylcarbamoyloxy)-3-(1-piperidyl)propyl] N-phenylcarbamate;hydrochloride represents a compelling area of study, bridging the fields of medicinal chemistry and pharmacology. Its unique structure and potential applications in health sciences make it a promising candidate for future investigations.
Synonyms
DIPERODON HYDROCHLORIDE
537-12-2
Proctodon
Diperocaine
Diperodon HCl
Diothane hydrochloride
Diperdon hydrochloride
EINECS 208-659-8
NSC 76069
5YZ5R8I73Y
DTXSID1045324
NSC-76069
3-Piperidino-1,2-propanediol dicarbanilate hydrochloride
3-(1-Piperidyl)-1,2-propanediol dicarbanilate hydrochloride
DTXCID9025324
DIPERODON HYDROCHLORIDE [MI]
DIPERODON HYDROCHLORIDE [VANDF]
DIPERODON HYDROCHLORIDE [MART.]
DIPERODON HYDROCHLORIDE [WHO-DD]
1,2-Propanediol, 3-piperidino-, dicarbanilate, hydrochloride
DIPERODON HYDROCHLORIDE [GREEN BOOK]
1,2-Propanediol, 3-piperidino-, dicarbanilate (ester), monohydrochloride
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamato) (ester), monohydrochloride
DIPERODON HYDROCHLORIDE (MART.)
1,2-PROPANEDIOL, 3-(1-PIPERIDINYL)-, 1,2-BIS(N-PHENYLCARBAMATE), HYDROCHLORIDE (1:1)
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride (9CI)
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamato) (ester), monohydrochloride (9CI)
1,2-Propanediol, 3-piperidino-, dicarbanilate (ester), monohydrochloride (8CI)
208-659-8
Diperodon (hydrochloride)
[2-(phenylcarbamoyloxy)-3-piperidin-1-ylpropyl] N-phenylcarbamate;hydrochloride
UNII-5YZ5R8I73Y
MDL 28574; 6-Butyryl castanospermine; Castanospermine 6-butyrate
Prestwick_673
d-Diothane hydrochloride
l-Diothane hydrochloride
dl-Diothane hydrochloride
NCGC00016500-01
CAS-537-12-2
MLS002154257
SCHEMBL1169004
CHEMBL1456312
NIOSH/TZ1103000
NIOSH/TZ1103100
NIOSH/TZ1103200
OWULVAZDMWJBLB-UHFFFAOYSA-N
HMS1568L22
Pharmakon1600-01505780
HY-B1226
NSC76069
Tox21_110460
NSC759247
s4397
AKOS024374933
Tox21_110460_1
CCG-213549
CS-4874
NSC-759247
NCGC00166142-04
DA-62908
SMR001233518
TS-07639
Diperodon hydrochloride, analytical standard
NS00079941
SW196828-3
TZ11030000
TZ11031000
TZ11032000
H38634
SR-01000841186
SR-01000841186-2
Q27263073
dl-Piperidinopropane-2,3-diol dicarbanilate hydrochloride
1, 3-piperidino-, dicarbanilate (ester), monohydrochloride
d-1-Piperidinopropane-2,3-diol dicarbanilate hydrochloride
l-1-Piperidinopropane-2,3-diol dicarbanilate hydrochloride
1, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride
3-(piperidin-1-yl)propane-1,2-diyl bis(phenylcarbamate) hydrochloride
(+)-3-(1-Piperidinyl)-1,2-propanediol bis(phenylcarbamate) (ester) monohydrochloride
(+-)-3-(1-Piperidinyl)-1,2-propanediol bis(phenylcarbamate) (ester) monohydrochloride
(-)-3-(1-Piperidinyl)-1,2-propanediol bis(phenylcarbamate) (ester) monohydrochloride
1,2-Propanediol, 3-piperidino-, dicarbanilate (ester), monohydrochloride, (+)-
1,2-Propanediol, 3-piperidino-, dicarbanilate (ester), monohydrochloride, (+-)-
1,2-Propanediol, 3-piperidino-, dicarbanilate (ester), monohydrochloride, (-)-
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride, (+)-
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride, (+-)-
1,2-Propanediol, 3-(1-piperidinyl)-, bis(phenylcarbamate) (ester), monohydrochloride, (-)-
Solubility of [2-(phenylcarbamoyloxy)-3-(1-piperidyl)propyl] N-phenylcarbamate; hydrochloride
The solubility of a compound can significantly influence its biological activity and effectiveness in various applications. In the case of [2-(phenylcarbamoyloxy)-3-(1-piperidyl)propyl] N-phenylcarbamate; hydrochloride, several considerations come into play:
As a case in point, it’s common for salts like hydrochlorides to be more soluble than their neutral counterparts. To sum up, understanding the solubility of [2-(phenylcarbamoyloxy)-3-(1-piperidyl)propyl] N-phenylcarbamate; hydrochloride is essential for optimizing its use in various chemical and pharmaceutical processes. As stated, “The right solvent can make all the difference.”