Conditions | Yield |
---|---|
With sodium methylate In methanol at 45℃; | 97% |
With sodium hydride In tetrahydrofuran; diethyl ether for 1.75h; | 93% |
With sodium In diethyl ether | 90% |
Conditions | Yield |
---|---|
With sodium thiomethoxide In methanol at 23℃; for 0.5h; | 81% |
Conditions | Yield |
---|---|
With sodium In N,N,N,N,N,N-hexamethylphosphoric triamide at 90℃; |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
In tetrahydrofuran at 23℃; Rate constant; |
Conditions | Yield |
---|---|
In tetrahydrofuran at 23℃; Rate constant; |
diphenyldisulfane
A
sodium thiophenolate
B
thioxanthen-9-one 10,10-dioxide
Conditions | Yield |
---|---|
In tetrahydrofuran at 22.4 - 33.5℃; Rate constant; Thermodynamic data; Ea, ΔG*, ΔS*; |
Conditions | Yield |
---|---|
In tetrahydrofuran at 23℃; Rate constant; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol for 0.5h; Heating; | |
With sodium In ammonia | |
With sodium tetrahydroborate In ethanol | |
With sodium tetrahydroborate In ethanol Inert atmosphere; |
diphenylthiophosphinic acid-S-phenyl ester
A
sodium thiophenolate
B
sodium diphenylphosphinate
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetonitrile at 25℃; Rate constant; effect of H2O-MeCN proportion; further base and solvent; |
2-Chloroethyl phenyl sulfide
toluene
A
ethene
B
1,2-bis(phenylthio)ethane
C
sodium thiophenolate
1-chloro-4-(phenylthio)butane
toluene
A
1-butylene
B
ethene
C
1,4-bis-phenylsulfanyl-butane
D
sodium thiophenolate
3-chloropropyl phenyl sulfide
toluene
A
1,3-bis(phenylthio)propane
B
sodium thiophenolate
C
cyclopropane
Conditions | Yield |
---|---|
With methanol | |
Stage #1: sodium With methanol Stage #2: thiophenol In methanol |
Conditions | Yield |
---|---|
With NaH In tetrahydrofuran | A 450 mg (34%) B n/a |
Conditions | Yield |
---|---|
In quinoline; dimethyl sulfoxide |
Conditions | Yield |
---|---|
With acetic acid In methanol; water; dimethyl sulfoxide |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol Inert atmosphere; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetic acid / ethanol / 3 h / Reflux; Inert atmosphere 2: acetic acid / water; dimethyl sulfoxide View Scheme |
3-nitro-N-phenylphthalimide
sodium thiophenolate
Conditions | Yield |
---|---|
With acetic acid In water; dimethyl sulfoxide |
Conditions | Yield |
---|---|
o-phenylene-bis-nickel(II) bromide In ethylene glycol at 200℃; for 24h; | 100% |
With 1,5-(2,9-dimethyl-1,10-phenanthroyl)-p-tert-butylcalix[8]arene; copper(l) chloride In toluene at 110℃; for 15h; Schlenk technique; Glovebox; Inert atmosphere; | 95% |
With tetra(n-butyl)ammonium hydroxide In ammonia at -45℃; for 1.5h; Irradiation; further catalyst (Et3N); | 70% |
With 2C21H11N3O6(4-)*H(1+)*2Ni(2+)*14H2O*Co(3+) In N,N-dimethyl-formamide at 80℃; for 6h; Reagent/catalyst; Inert atmosphere; | 65 %Chromat. |
Conditions | Yield |
---|---|
In tetrahydrofuran Ambient temperature; | 100% |
5-chloropentyl acetate
sodium thiophenolate
5-(phenylthio)pentyl acetate
Conditions | Yield |
---|---|
In ethanol at 80℃; for 2h; | 100% |
carvotanacetone
sodium thiophenolate
5-isopropyl-2-methyl-3-(phenylthio)cyclohexanone
Conditions | Yield |
---|---|
In tetrahydrofuran Ambient temperature; | 100% |
4-Nitrophthalonitrile
sodium thiophenolate
3-(phenylthio)-phthalonitrile
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 100% |
3,4,5,6-tetramethyl-1,2-dinitrobenzene
sodium thiophenolate
1-nitro-2-(phenylthio)-3,4,5,6-tetramethylbenzene
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 120℃; for 0.25h; | 100% |
1-nitro-2-(phenylsulfonyl)benzene
sodium thiophenolate
2-nitrophenyl phenyl sulfide
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 120℃; for 3h; | 100% |
sodium thiophenolate
E-(1-methyl 1,3-butadienyl) sulfonyl benzene
E-(1-methyl 4-phenylthio 2-butenyl) sulfonyl benzene
Conditions | Yield |
---|---|
In ethanol; benzene at 25℃; for 3h; | 100% |
sodium thiophenolate
Methyl 2-cyclopentyl-6-bromo-4-hexenoate
Methyl 2-cyclopentyl-6-phenylthio-4-hexenoate
Conditions | Yield |
---|---|
In ethanol | 100% |
sodium thiophenolate
Methyl trans-1-(4-bromo-2-butenyl)cyclohexanecarboxylate
Methyl 1-(4-phenylthio-2-butenyl)-cyclohexanecarboxylate
Conditions | Yield |
---|---|
In ethanol | 100% |
sodium thiophenolate
acetic acid (2Z,6E)-8-bromo-3,7-dimethyl-octa-2,6-dienyl ester
(2Z,6E)-3,7-dimethyl-8-phenylthio-2,6-octadien-1-ol
Conditions | Yield |
---|---|
In methanol at 65℃; for 2h; | 100% |
sodium thiophenolate
Conditions | Yield |
---|---|
In methanol for 2h; Heating; | 100% |
sodium thiophenolate
1-bromo-2,2-dimethylcyclopropyl methyl sulfide
(2,2-Dimethyl-1-methylsulfanyl-cyclopropylsulfanyl)-benzene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium perchlorate In methanol at 20 - 25℃; for 24h; | 100% |
sodium thiophenolate
Conditions | Yield |
---|---|
With hydrogenchloride; sodium perchlorate In methanol at 20 - 25℃; for 24h; | 100% |
tetrabutyl-ammonium chloride
sodium thiophenolate
tetra-N-butylammonium benzenethiolate
Conditions | Yield |
---|---|
In tetrahydrofuran for 4h; Inert atmosphere; | 100% |
sodium thiophenolate
6,8-dibromo-1,4-dimethoxybenzocyclohepten-7-one
6,8-bis(phenylthio)-1,4-dimethoxy-7H-benzocyclohepten-6-one
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 85℃; for 1h; | 100% |
sodium thiophenolate
9-<2,3-anhydro-5-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl>adenine
9-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3-C-phenylthio-β-D-xylofuranosyl]adenine
Conditions | Yield |
---|---|
In methanol for 6.5h; Heating; | 100% |
2-chlorobenzo[d][1,3]thiazole
sodium thiophenolate
2-(phenylthio)benzothiazole
Conditions | Yield |
---|---|
In ethanol for 5h; Heating; | 100% |
sodium thiophenolate
4-[(tert-butyldimethylsilyl)oxy]but-2-yn-1-yl 4-methylbenzene-1-sulfonate
tert-butyl-dimethyl-(4-phenylsulfanyl-but-2-ynyloxy)-silane
Conditions | Yield |
---|---|
With 18-crown-6 ether In toluene at 20℃; | 100% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 60℃; for 4h; | 100% |
sodium thiophenolate
cis-(2S,3S)-(+)-N-(p-toluenesulfonyl)-2-carbomethoxy-3-phenylaziridine
Conditions | Yield |
---|---|
100% |
sodium thiophenolate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; a mixt. of Ti-compd. and NaSPh in THF is stirred for 1 h (N2); solvent is removed, residue is extd. into benzene, ppt. is filtered off, filtrate is kept for 1 week, elem. anal.; | 100% |
sodium thiophenolate
N-methyl-tri-n-butyl-ammonium bromide
methyl-phenyl-thioether
Conditions | Yield |
---|---|
In butan-1-ol at 115℃; for 5h; | 99.5% |
Conditions | Yield |
---|---|
In N,N,N,N,N,N-hexamethylphosphoric triamide at 90℃; for 0.00972222h; microwave irradiation; | 99% |
In ethanol Heating; | 89% |
In dimethyl sulfoxide at 150℃; for 0.25h; Microwave irradiation; | 83% |
With ethanol |
Conditions | Yield |
---|---|
In N,N,N,N,N,N-hexamethylphosphoric triamide at 100℃; for 0.00833333h; microwave irradiation; | 99% |
In N,N-dimethyl-formamide at 80℃; for 4h; Product distribution; Mechanism; | 58 % Chromat. |
In N,N-dimethyl-formamide at 80℃; for 4h; | 58 % Chromat. |
Conditions | Yield |
---|---|
dodecyldimethylsulfonium methyl sulfate In water at 40℃; for 6h; | 99% |
polymer-supported polyether 6a In water; toluene at 25℃; Rate constant; other polymer-supported crown ethers and cryptands as phase-transfer catalysts; | |
hexadecyltetrabutylphosphonium bromide at 20℃; for 0.15h; Product distribution; further times and phase-transfer catalysts; | 100 % Chromat. |
Ph3S(1+)*X(1-); bromine; iodide; perchlorate(1-) In dichloromethane; water at 40℃; for 12h; |
p-(1-methyl-1-nitropropyl)nitrobenzene
sodium thiophenolate
A
2-(p-nitrophenyl)-2-butyl phenyl sulfide
B
diphenyldisulfane
Conditions | Yield |
---|---|
In dimethyl sulfoxide for 0.75h; | A 99% B 99% |
2-(Chloromethyl)-cyclopropannitril
sodium thiophenolate
2-Phenylsulfanylmethyl-cyclopropanecarbonitrile
Conditions | Yield |
---|---|
In methanol for 16h; Heating; | 99% |
sodium thiophenolate
(2-bromo-1,1-difluoro-ethyl)benzene
2,2-Difluoro-2-phenylethyl phenyl sulfide
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide at 25℃; for 2h; | 99% |
The cas register number of Sodium thiophenolate is 930-69-8. It also can be called as Benzenethiol, sodium salt and the Systematic name about this chemical is sodium benzenethiolate.
Physical properties about Sodium thiophenolate are: (1)ACD/LogP: 2.52; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.49; (4)ACD/LogD (pH 7.4): 1.67; (5)ACD/BCF (pH 5.5): 44.97; (6)ACD/BCF (pH 7.4): 6.83; (7)ACD/KOC (pH 5.5): 519.58; (8)ACD/KOC (pH 7.4): 78.9; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 38.8Å2; (13)Flash Point: 50.6 °C; (14)Enthalpy of Vaporization: 39.93 kJ/mol; (15)Boiling Point: 169.1 °C at 760 mmHg; (16)Vapour Pressure: 2.07 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
It can causes burns. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. So people must 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.)
People can use the following data to convert to the molecule structure.
1.SMILES: [Na+].[S-]c1ccccc1
2.InChI: InChI=1/C6H6S.Na/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1
3.InChIKey: RZWQDAUIUBVCDD-REWHXWOFAQ
4.Std. InChI: InChI=1S/C6H6S.Na/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1.
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