Interesting facts
Interesting Facts About (1-ethyl-1-methyl-propyl) Carbamate
(1-ethyl-1-methyl-propyl) carbamate, often simply referred to as a carbamate derivative, is a fascinating compound that plays a significant role in various fields of chemistry, particularly in agrochemistry and medicinal chemistry. Here are some interesting insights:
- Chemical Classification: This compound belongs to the carbamate family, which are esters of carbamic acid. Carbamates are widely recognized for their applications as herbicides, insecticides, and pesticides in agriculture.
- Biological Activity: Many carbamates, including this one, exhibit interesting biological properties. They can act as enzyme inhibitors, particularly of the acetylcholinesterase enzyme, which is crucial in nerve function.
- Industrial Relevance: Due to their stability and efficacy, carbamates are used in several industrial applications, including the manufacture of plastics, coatings, and pharmaceuticals.
- Synthetic Routes: The synthesis of (1-ethyl-1-methyl-propyl) carbamate can involve various methods, including the reaction of isocyanates with alcohols. This presents exciting opportunities to explore green chemistry methods for production.
- Environmental Considerations: The environmental impact of carbamate compounds is a topic of ongoing research. Understanding their biodegradation pathways is crucial for mitigating ecological risks.
With its diverse applications and remarkable properties, (1-ethyl-1-methyl-propyl) carbamate serves as a compelling subject of study, highlighting the intricate connections between chemistry, biology, and environmental science. As scientists continue to explore its potential benefits and drawbacks, it remains a vital compound within both industrial and academic circles.
Synonyms
Emylcamate
78-28-4
Emilcamato
Emylcamat
3-methylpentan-3-yl carbamate
Nuncital
Psicoplegil
Restetal
Stratran
Striatan
Striatran
Statran
1-Ethyl-1-methylpropyl carbamate
tert-Hexanol carbamate
3-Methyl-3-pentanol carbamate
KABI-925
Kabi-295
tert-Hexyl carbamate
Diethyl methyl carbinol urethan
MK-250
Methyl diethyl carbinol urethan
Emylcamatum
91 JD
JD-91
3-Pentanol, 3-methyl-, carbamate
Emylcamate [INN:BAN]
Carbamic acid, tert-hexyl ester
Emylcamatum [INN-Latin]
Emilcamato [INN-Spanish]
KABI 925
Stratan
NSC 169882
CARBAMIC ACID, 1-ETHYL-1-METHYLPROPYL ESTER
terc.Hexylester kyseliny karbaminove
EINECS 201-101-4
UNII-KCJ747D3R4
Emylcamate (INN)
NSC-169882
BRN 1755436
KCJ747D3R4
terc.Hexylester kyseliny karbaminove [Czech]
EMYLCAMATE [MI]
EMYLCAMATE [INN]
EMYLCAMATE [WHO-DD]
DTXSID40228645
4-03-00-00058 (Beilstein Handbook Reference)
3-Pentanol, carbamate
Emylcamatum (INN-Latin)
Emilcamato (INN-Spanish)
WLN: ZVOX2&2&1
KAB 1925
3-Pentanol, 3-methyl-, carbamate (8CI)
SCHEMBL387718
CHEMBL2104208
DTXCID90151136
N05BC03
CHEBI:134769
AAA07828
NSC169882
NSC169917
AKOS006273433
DB13572
NSC-169917
DA-63179
HY-121340
CS-0081492
NS00037982
D07317
EN300-212804
3-Pentanol, 3-methyl-, carbamate (8CI)(9CI)
Q378997
Z1198155508
201-101-4
Solubility of (1-ethyl-1-methyl-propyl) carbamate
(1-ethyl-1-methyl-propyl) carbamate exhibits interesting characteristics regarding its solubility, primarily dependent on its **polarity** and **functional groups**. The presence of the carbamate functional group enhances its potential for solubility in various solvents.
Solubility in Water
As a member of the carbamate family, (1-ethyl-1-methyl-propyl) carbamate has some degree of solubility in water due to hydrogen bonding capabilities. Here are some key points:
Solubility in Organic Solvents
This compound is likely to show a higher solubility in organic solvents due to its alkyl groups' hydrophobic nature. The following characteristics can be noted:
In summary, the solubility of (1-ethyl-1-methyl-propyl) carbamate is marked by its dual nature: it has a reasonable solubility in water while favoring organic solvents due to its molecular structure. Understanding this solubility behavior is crucial for its applications in various chemical processes.