Conditions | Yield |
---|---|
With sodium for 48h; Ambient temperature; | 90% |
With diethyl ether; sodium | |
With sodium Yield given; |
Diethyl disulfide
diethyl ether
1,2-disodiotetraphenylethane
A
1,1,2,2-tetraphenylethylene
B
sodium thioethylate
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol for 1.5h; Heating; |
S-ethyl diphenylphosphorothiolate
A
sodium diphenylphosphinate
B
sodium thioethylate
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetonitrile at 25℃; Rate constant; effect of H2O-MeCN proportion; further base and solvent; |
3-(ethylthio)propyl chloride
toluene
A
3,7-dithianonane
B
cyclopropane
C
sodium thioethylate
{PPN}{EtSFe(CO)4}
{PPN}{SPh}
{PPN}{PhSFe(CO)4}
B
sodium thioethylate
Conditions | Yield |
---|---|
With Na(1+) In tetrahydrofuran presence of Na(1+), 10 min, pptn of EtSNa; |
o-ethylmercapto-benzonitrile
sodium thioethylate
Conditions | Yield |
---|---|
Stage #1: o-ethylmercapto-benzonitrile With hydrogenchloride; water; chlorine In chlorobenzene at 45 - 70℃; for 3h; Stage #2: With sodium hydrogen sulfide; tetrabutylammomium bromide In water; chlorobenzene at 30℃; for 7h; Inert atmosphere; | 74 g |
2-chloro-6-(methylsulfonyl)pyridine
sodium thioethylate
2-chloro-6-ethylsulphenylpyridine
Conditions | Yield |
---|---|
With 18-crown-6 ether In benzene for 0.25h; Heating; | 100% |
In ethanol for 1.5h; Ambient temperature; | 90% |
diethyl chlorophosphate
sodium thioethylate
O,O,S-triethyl phosphorothioate
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 1.5h; | 100% |
4-bromoethylbutanoate
sodium thioethylate
4-ethylthiobutyric acid ethyl ester
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 0 - 20℃; for 15h; | 100% |
carbon disulfide
sodium thioethylate
bis(ethylsulfanyl thiocarbonyl)disulfide
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; sodium thioethylate In diethyl ether at 0 - 20℃; Stage #2: With iodine In diethyl ether at 20℃; for 2h; | 100% |
Stage #1: carbon disulfide; sodium thioethylate In diethyl ether at 0 - 20℃; for 2h; Stage #2: With iodine In diethyl ether at 20℃; for 2h; | 78.8% |
sodium thioethylate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 5h; Inert atmosphere; | 100% |
sodium thioethylate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 6h; Reflux; | 100% |
sodium thioethylate
Conditions | Yield |
---|---|
In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 2h; | 100% |
6-chloro-pyridazin-3-ylamine
sodium thioethylate
3-amino-6-ethylthiopyridazine
Conditions | Yield |
---|---|
In ethanol for 53h; Heating; | 99% |
Conditions | Yield |
---|---|
In methanol N2-atmosphere; mixing Ni-complex with excess NaSEt, filtration (after 1 d), addn. of excess Bu4NCl; crystn. (-30°C, 3 d), collection (filtration), washing (THF, hexane), drying (vac., 2 h); elem. anal.; | 99% |
sodium thioethylate
(3-bromo-4-(2,4-difluorophenoxy)benzyl)(ethyl)sulfane
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 4h; | 99% |
In N,N-dimethyl-formamide at 20℃; for 4h; Inert atmosphere; | 99% |
In N,N-dimethyl-formamide at 20℃; for 4h; | 1.30 g |
In N,N-dimethyl-formamide at 20℃; for 6h; |
1-benzyl-3-(2-bromoethyl)-1H-imidazol-3-ium bromide
sodium thioethylate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 15h; Schlenk technique; Inert atmosphere; | 99% |
In acetonitrile at 25℃; Inert atmosphere; Schlenk technique; | 99% |
sodium thioethylate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 3h; | 99% |
N-Mesyloxytroponimine
sodium thioethylate
Conditions | Yield |
---|---|
In tetrahydrofuran; ethanol at -20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 90 - 100℃; | A 98% B n/a |
sodium thioethylate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 1h; | 98% |
1-benzyl-3,5-dichloro-6-methylpyrazin-2(1H)-one
sodium thioethylate
1-benzyl-5-chloro-3-(ethylsulfanyl)-6-methyl-2(1H)-pyrazinone
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 97% |
4-(1,3-Dioxan-2-yl)-3-fluorobenzonitrile
sodium thioethylate
4-(1,3-Dioxan-2-yl)-3-(ethylsulfanyl)benzonitrile
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20 - 100℃; for 5h; Inert atmosphere; | 97% |
sodium thioethylate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 2h; Cooling with ice; | 97% |
N-(3-Azido-propyl)-4-(benzotriazol-1-yl-phenylacetylamino-methyl)-benzamide
sodium thioethylate
N-(3-Azido-propyl)-4-(ethylsulfanyl-phenylacetylamino-methyl)-benzamide
Conditions | Yield |
---|---|
In tetrahydrofuran for 4h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide at 0℃; for 10h; | 96% |
(S)-3-(2-fluoro-6-methoxy-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester
sodium thioethylate
(S)-3-(2-fluoro-6-hydroxy-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: (S)-3-(2-fluoro-6-methoxy-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester; sodium thioethylate In 1-methyl-pyrrolidin-2-one at 100℃; for 8h; Stage #2: With water In 1-methyl-pyrrolidin-2-one; diethyl ether; sodium chloride | 96% |
C11H13BrO4
sodium thioethylate
Conditions | Yield |
---|---|
In tetrahydrofuran at 0℃; for 2h; | 96% |
2-fluoro-5-[2-phenyl-4-(pyridin-4-yl)-1H-imidazol-5-yl]benzoic acid
sodium thioethylate
2-(ethylthio)-5-[2-phenyl-4-(pyridin-4-yl)-1H-imidazol-5-yl]benzoic acid
Conditions | Yield |
---|---|
Stage #1: 2-fluoro-5-[2-phenyl-4-(pyridin-4-yl)-1H-imidazol-5-yl]benzoic acid; sodium thioethylate With caesium carbonate In ISOPROPYLAMIDE at 90℃; for 4h; Stage #2: With hydrogenchloride In ISOPROPYLAMIDE; water pH=4.5; | 96% |
N-(2-acetylphenyl)-2-propenamide
sodium thioethylate
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 60℃; for 4h; | 96% |
sodium thioethylate
Conditions | Yield |
---|---|
In tetrahydrofuran at -5℃; for 2h; | 96% |
5,6-dichloro-2-pyridinecarboxylic acid
sodium thioethylate
5,6-bis-ethylpyridine-2-carboxylic acid
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 130 - 135℃; for 2h; | 95% |
bronidox
sodium thioethylate
A
Diethyl disulfide
B
5-nitro-5-(5-nitro-1,3-dioxa-5-cyclohexyl)-1,3-dioxacyclohexane
Conditions | Yield |
---|---|
In dimethyl sulfoxide for 3h; Ambient temperature; | A 95% B 90% |
5-nitro-5-(5-nitro-1,3-dioxa-5-cyclohexyl)-1,3-dioxacyclohexane
sodium thioethylate
A
Diethyl disulfide
B
5-(1,3-dioxa-5-cyclohexylidene)-1,3-dioxane
Conditions | Yield |
---|---|
for 3h; | A 95% B 92% |
Conditions | Yield |
---|---|
In dichloromethane at 40℃; for 3h; | 95% |
In dichloromethane at 30℃; for 3h; Yield given; |
2-carboxymethyl-3-trifluoromethansulfonyloxy-5α-cholest-2-eno
ethanethiol
sodium thioethylate
(5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-3-ethylsulfanyl-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2-carboxylic acid methyl ester
Conditions | Yield |
---|---|
for 15h; Ambient temperature; | 95% |
The CAS register number of Ethanethiol, sodiumsalt (1:1) is 811-51-8. It also can be called as Sodium ethyl mercaptide and the systematic name about this chemical is sodium ethanethiolate. The molecular formula about this chemical is C2H5NaS and the molecular weight is 84.12.
When you are using this chemical, please be cautious about it as the following:
This chemical is corrosive and it can cause burns and destroy living tissue on contact. When contact with water, it can liberate toxic gas. If you want to use it, wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) What`s more, in case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: CCS[Na]
(2)InChI: InChI=1/C2H6S.Na/c1-2-3;/h3H,2H2,1H3;/q;+1/p-1/rC2H5NaS/c1-2-4-3/h2H2,1H3
(3)InChIKey: QJDUDPQVDAASMV-LGPHYPBZAI
(4)Std. InChI: InChI=1S/C2H6S.Na/c1-2-3;/h3H,2H2,1H3;/q;+1/p-1
(5)Std. InChIKey: QJDUDPQVDAASMV-UHFFFAOYSA-M
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