Interesting facts
Interesting Facts about (1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide
(1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide is a fascinating compound that resides at the intersection of organic chemistry and pharmacology. This unique compound showcases the diverse properties and functionalities that can arise from the combination of aromatic structures and functional groups.
Key Characteristics:
- Pyridinic Influence: The presence of a pyridine ring enhances the compound's reactivity and interaction with biological systems, making it of particular interest in medicinal chemistry.
- Quaternary Ammonium Ion: The quaternization of nitrogen in the pyridine system contributes to increased solubility in polar solvents and can influence its biological activity.
- Carbamate Group: The carbamate moiety is known for its roles in both herbicides and pharmaceuticals, emphasizing its importance in agriculture and health sectors.
This compound has garnered attention for its potential applications, including:
- Development of novel neurotransmitter inhibitors that may offer therapeutic benefits.
- Integration in formulations aimed at enhancing agricultural practices by acting as effective biocides.
- Exploration in synthetic pathways for related compounds that may lead to groundbreaking discoveries in chemical synthesis.
As we learn more about compounds like (1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide, we unlock the doors to innovative research avenues. This compound exemplifies how meticulous chemical design can lead to products with significant industrial and therapeutic potential.
Synonyms
PYRIDOSTIGMINE BROMIDE
101-26-8
Mestinon
Kalimin
Kalymin
Regonol
3-(Dimethylcarbamoyloxy)-1-methylpyridinium Bromide
Regonal
Mestinon bromide
3-((Dimethylcarbamoyl)oxy)-1-methylpyridin-1-ium bromide
Pyridostigmini bromidum
Bromure de pyridostigmine
Bromuro de piridostigmina
Piridostigmina bromuro
CCRIS 6798
Pyridostigmine (bromide)
HSDB 3924
EINECS 202-929-9
UNII-KVI301NA53
MFCD00079283
NSC-679759
NSC-758435
Ro 1-5130
KVI301NA53
DTXSID9023540
Pyridinium, 3-(((dimethylamino)carbonyl)oxy)-1-methyl-, bromide
3-Hydroxy-1-methylpyridinium bromide dimethylcarbamate
Pyridostigmini bromidum [INN-Latin]
3-(Dimethylcarbamyloxy)-1-methylpyridinium bromide
Bromure de pyridostigmine [INN-French]
Bromuro de piridostigmina [INN-Spanish]
1-Methyl-3-hydroxypyridinium bromide dimethylcarbamate
MLS000028385
RO-1-5130
3-[(dimethylcarbamoyl)oxy]-1-methylpyridin-1-ium bromide
DTXCID503540
(1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate;bromide
3-(((Dimethylamino)carbonyl)oxy)-1-methylpyridinium bromide
3-Hydroxy-1-methylpyridinium bromide dimethylcarbamate (ester)
Pyridinium, 3-hydroxyl-1-methyl-, bromide, dimethylcarbamate
Pyridinium, 3-[[(dimethylamino)carbonyl]oxy]-1-methyl-, bromide
Dimethylcarbamic acid ester of 3-hydroxy-1-methylpyridinium bromide
Carbamic acid, dimethyl-, ester with 3-hydroxy-1-methylpyridinium bromide
NSC679759
NSC 758435
NCGC00094324-02
SMR000058605
Pyridostigmine bromide [USP:INN:BAN:JAN]
Pyridinium, 3-hydroxy-1-methyl-, bromide, dimethylcarbamate (ester)
3-(Dimethylaminocarbonyloxy)-1-methylpyridinium bromide
CHEMBL812
Pyridostigmini bromidum (INN-Latin)
Pyridinium, 3-[[(dimethylamino)carbonyl]oxy]-1-methyl-, bromide (1:1)
PYRIDOSTIGMINE BROMIDE (MART.)
PYRIDOSTIGMINE BROMIDE [MART.]
PYRIDOSTIGMINE BROMIDE (USP-RS)
PYRIDOSTIGMINE BROMIDE [USP-RS]
Bromure de pyridostigmine (INN-French)
PYRIDINIUM, 3-(((DIMETHYLAMINO)CARBONYL)OXY)-1-METHYL-, BROMIDE (1:1)
Bromuro de piridostigmina (INN-Spanish)
3-Dimethylcarbamoyloxy-1-methylpyridinium bromide;3-Dimethylcarbamoyloxy-1-methylpyridinium bromide
CAS-101-26-8
Piridostigmina bromuro [DCIT]
PYRIDOSTIGMINE BROMIDE (EP IMPURITY)
Pyridostigmine bromide (USP:INN:BAN:JAN)
PYRIDOSTIGMINE BROMIDE [EP IMPURITY]
PYRIDOSTIGMINE BROMIDE (EP MONOGRAPH)
PYRIDOSTIGMINE BROMIDE [EP MONOGRAPH]
PYRIDOSTIGMINE BROMIDE (USP MONOGRAPH)
PYRIDOSTIGMINE BROMIDE [USP MONOGRAPH]
Bromide, Pyridostigmine
SR-01000003072
3-{[(dimethylamino)carbonyl]oxy}-1-methylpyridinium bromide
Mestinon (TN)
Pryidostigmine Bromide
pyridostigminii bromidum
pyridostigmine (cation)
Opera_ID_420
Pyridostigmine bromide oral
SCHEMBL41147
MLS001074080
SPECTRUM1503240
CHEBI:8666
HY-B0207AR
HMS500K09
HY-B0207A
N07AA02
Pyridostigmine Bromide (Mestinon)
VNYBTNPBYXSMOO-UHFFFAOYSA-M
HMS1922M05
HMS2092P14
HMS2234D06
HMS3259M16
HMS3263O11
HMS3369P02
HMS3651G13
HMS3884M21
Pharmakon1600-01503240
PYRIDOSTIGMINE BROMIDE [MI]
AVD85808
BCP02148
Pyridostigmine (bromide) (Standard)
PYRIDOSTIGMINE BROMIDE [INN]
PYRIDOSTIGMINE BROMIDE [JAN]
Tox21_111266
Tox21_501035
CCG-40306
NSC758435
PYRIDOSTIGMINE BROMIDE [HSDB]
s1608
AKOS015895321
Tox21_111266_1
AC-8143
FP27317
LP01035
NC00581
PYRIDOSTIGMINE BROMIDE [WHO-DD]
PYRIDOSTIGMINE BROMIDE [WHO-IP]
NCGC00015862-07
NCGC00094324-01
NCGC00094324-03
NCGC00094324-04
NCGC00261720-01
Pyridostigmine bromide (JP18/USP/INN)
AS-13164
SY108979
PYRIDOSTIGMINE BROMIDE [ORANGE BOOK]
EU-0101035
NS00079096
P1339
SW199029-2
PYRIDOSTIGMINI BROMIDUM [WHO-IP LATIN]
D00487
EN300-120686
P 9797
T71526
3-Dimethylcarbamoyloxy-1-methylpyridinium bromide
SR-01000003072-2
SR-01000003072-4
3-[(Dimethylcarbamoyl)oxy]-1-methylpyridinium Bromide
Q26840825
3-((Dimethylcarbamoyl)oxy)-1-methylpyridin-1-iumbromide
Z1269171738
Carbamic Acid,Dimethyl-, Ester with 3-Hydroxy-1-methylpyridinium Bromide
Pyridostigmine bromide, European Pharmacopoeia (EP) Reference Standard
Pyridostigmine bromide, United States Pharmacopeia (USP) Reference Standard
Pyridostigmine bromide; 3-[[(Dimethylamino)carbonyl]oxy]-1-methylpyridinium bromide
202-929-9
Solubility of (1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide
The solubility of (1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide is influenced by a variety of factors, primarily due to its ionic and polar characteristics. Key points to consider include:
In summary, the solubility of (1-methylpyridin-1-ium-3-yl) N,N-dimethylcarbamate; bromide is likely to be high in water and other polar solvents. This characteristic makes it essential for applications in various chemical processes.