Interesting facts
Interesting Facts about S-ethyl azepane-1-carbothioate
S-ethyl azepane-1-carbothioate is a fascinating compound that belongs to the class of thioesters, known for their role in various synthetic and biological processes. Here are some remarkable insights about this compound:
- Structure and Functionality: S-ethyl azepane-1-carbothioate contains a unique seven-membered ring structure (azepane) that contributes to its reactivity and stability. Its thioester functional group (-C(=O)S-) is particularly significant in biochemical processes, such as enzyme catalysis.
- Biological Importance: Compounds like S-ethyl azepane-1-carbothioate can serve as precursors for biologically active molecules. In nature, similar thioesters play crucial roles in cellular metabolism and the biosynthesis of various natural products.
- Synthetic Utility: The compound can act as a versatile building block in organic synthesis. Its ability to participate in nucleophilic acyl substitution reactions makes it valuable for creating complex organic molecules.
- Odor and Flavor Chemistry: Thioesters, including S-ethyl azepane-1-carbothioate, can impart distinct odors and flavors, which find applications in the fragrance and food industries. The unique scent profile of this compound could lead to interesting applications in those fields.
As a Chemistry Student or a Research Scientist, understanding compounds like S-ethyl azepane-1-carbothioate broadens your appreciation of the chemical world and opens doors to innovative research opportunities. Its combination of structural uniqueness and functional versatility exemplifies the intricate interplay of chemistry and biological processes.
Synonyms
MOLINATE
2212-67-1
Ordram
S-Ethyl azepane-1-carbothioate
Jalan
Yalan
Yulan
Higalnate
Hydram
Molmate
Felan
Sakkimol
S-Ethyl hexahydro-1H-azepine-1-carbothioate
Molinate estrella
Stauffer R-4,572
Ethyl 1-hexamethyleneiminecarbothiolate
S-Ethyl N,N-hexamethylenethiocarbamate
S-Ethyl hexahydroazepine-1-carbothioate
Malerbane Giavoni L
1H-Azepine-1-carbothioic acid, hexahydro-, S-ethyl ester
S-Ethyl-N-hexamethylenethiocarbamate
Caswell No. 444
Molinate [BSI:ISO]
S-Ethyl 1-hexamethyleneiminothiocarbamate
Perhydroazepin-1-carbothioate
R-4572
68N5G08DJQ
CHEBI:6964
HSDB 873
S-Ethyl perhydroazepine-1-thiocarboxylate
DTXSID6024206
MOLINATE [HSDB]
MOLINATE [ISO]
MOLINATE [MI]
EINECS 218-661-0
R 4572
SC 998
S-Ethyl perhydroazepin-1-carbothioate
EPA Pesticide Chemical Code 041402
S-Ethyl N,N-hexamethylenothiocarbamate
S-Ethyl-N,N-hexamethylenethiocarbamate
BRN 1239196
UNII-68N5G08DJQ
CCRIS 8083
DTXCID204206
S-Aethyl-N-hexahydro-1H-azepinthiolcarbamat
S-Aethyl-N-hexahydro-1H-azepinthiolcarbamat [German]
S-ethyl perhydroazepine-1-carbothioate
SC-9908
Ialan
5-20-04-00034 (Beilstein Handbook Reference)
C9H17NOS
S-ethyl 1-hexamethylenaminothiocarbamate
Ordam
Molinic acid
hexahydro-1H-azepine-1-carbothioic acid S-ethyl ester
Stauffer R4,572
S-ethyl 1-hexamethylenamino-thiocarbamate
SEthyl azepane1carbothioate
S-Ethyl 1-azepanecarbothioate
SEthylNhexamethylenethiocarbamate
SEthyl perhydroazepin1carbothioate
SEthylN,Nhexamethylenethiocarbamate
SEthyl hexahydroazepine1carbothioate
azepan-1-yl(ethylsulfanyl)methanone
SEthyl N,Nhexamethylenethiocarbamate
Ethyl 1hexamethyleneiminecarbothiolate
SAethylNhexahydro1Hazepinthiolcarbamat
SEthyl perhydroazepine1thiocarboxylate
SEthyl hexahydro1Hazepine1carbothioate
SEthyl 1hexamethyleneiminothiocarbamate
R4572
1HAzepine1carbothioic acid, hexahydro, Sethyl ester
1H-AZEPINE-1 CARBOTHIOIC ACID, HEXAHYDRO-S-ETHYL ESTER
1H-AZEPINE-1-CARBOTHIOIC ACID, HEXAHYDRO-S-ETHYL ESTER
S-ETHYL ESTER HEXAHYDRO-1H-AZEPINE-1-CARBOTHIOIC ACID
218-661-0
dedopgxggqyymw-uhfffaoysa-n
CAS-2212-67-1
SCHEMBL63895
MLS001065581
BIDD:ER0419
CHEMBL1865916
S-Ethyl 1-azepanecarbothioate #
HMS3039B07
Tox21_201572
Tox21_300817
MFCD00055352
Molinate 10 microg/mL in Cyclohexane
AKOS006230487
KS-5374
Molinate 100 microg/mL in Cyclohexane
NCGC00091443-01
NCGC00091443-02
NCGC00091443-03
NCGC00091443-04
NCGC00091443-05
NCGC00254721-01
NCGC00259121-01
AS-13882
SMR000568482
DB-045809
Molinate, PESTANAL(R), analytical standard
NS00000706
Q1943471
Solubility of S-ethyl azepane-1-carbothioate
S-ethyl azepane-1-carbothioate, with its unique structure, presents interesting solubility characteristics that are pivotal for its applications in various chemical processes. Understanding the solubility of this compound can guide researchers and industrial chemists in effectively utilizing it.
Key Points Regarding Solubility:
To summarize, while S-ethyl azepane-1-carbothioate shows promising solubility profiles in certain organic solvents, its performance in water is likely constrained. As always, it is recommended to conduct empirical solubility tests for precise applications in laboratory settings.