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Cas:75-15-0
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Carbon disulfide CAS: 75-15-0 Specification mp -112--111 °c(lit.) bp 46 °c(lit.) density 1.266 g/ml at 25 °c vapor density 2.67 (vs air) vapor pressure 5.83 psi ( 20 °c)
Product Detail Minimum Order Qty. 10 Gram
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inquiryAppearance:colourless to light yellow liquid with... Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:C
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A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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C-5263 Carbon disulfideAppearance:Colorless transparent liquid Application:The product is an important raw material for producing Viscose Fiber, Rubber Accelerator, Agricultur
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High purity Carbon disulfide 98% TOP1 supplier in China CAS NO.75-15-0 Application:High purity Carbon disulfide 98% TOP1 supplier in China CAS NO.75-15-0
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inquiryHigh purity&quality Carbon disulphide Application:phama
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inquiryCarbon disulphide Basic information Product Name: Carbon disulphide Synonyms: Alcohol of sulfur;Carbon bisulfuret;Carbon bisulphide;Carbon sulfide;Carbon sulfid
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inquirytetrachloromethane
sulfur
A
disulfur dichloride
B
carbon disulfide
Conditions | Yield |
---|---|
byproducts: S(x)Cl2; (N2), bomb reed, heated at 250°C for 24 h; cooled in liquid air in vac., distd.; | A 95% B n/a |
byproducts: S(x)Cl2; (N2), bomb reed, heated at 250°C for 15 h; cooled in liquid air in vac., distd.; | A 86% B n/a |
byproducts: S(x)Cl2; (N2), bomb reed, heated at 210°C for 8 d; cooled in liquid air in vac., distd.; | A 70% B n/a |
methanol
methylthiol
A
carbon disulfide
B
Dimethyldisulphide
C
dimethyltrisulfane
Conditions | Yield |
---|---|
Stage #1: methanol; methylthiol With hydrogen sulfide; aluminum oxide with 14percent by weight of potassium tungstate at 400℃; Stage #2: With sulfur; N-cyclohexyl-cyclohexanamine | A n/a B 94.9% C n/a |
Conditions | Yield |
---|---|
In melt at 180℃; for 0.166667h; Inert atmosphere; | A n/a B 88% |
sulfur dioxide
A
carbon disulfide
B
disulfur
C
carbon oxide sulfide
Conditions | Yield |
---|---|
byproducts: CO, CO2; at 1400 K, with excess of carbon; | A 81.16% B 10.82% C 8.02% |
byproducts: CO, CO2; at 1000 K, with excess of carbon; | A 37.08% B 3.22% C 59.7% |
sulfur
chloroform
A
hydrogenchloride
B
disulfur dichloride
C
carbon disulfide
Conditions | Yield |
---|---|
(N2), bomb reed, heated at 205°C for 60 h; cooled in liquid air in vac. for a week, distd.; Raman spectr.; | A n/a B 80% C n/a |
Conditions | Yield |
---|---|
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C; catalyst: asbestos powder;; | A n/a B 71.5% |
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C;; | A n/a B 58% |
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C;; | A n/a B 22.1% |
bis (2-chloroethyl) sulphide
acetylene
A
thiophene
B
carbon disulfide
C
Benzo[b]thiophene
D
benzene
Conditions | Yield |
---|---|
With disulfide oil at 650℃; for 1.75h; Further byproducts given; | A 68% B 0.09 g C 0.12 g D 0.25 g |
thiourea
A
carbon disulfide
Conditions | Yield |
---|---|
With tetraphosphorus decasulfide at 140℃; for 40h; | A n/a B 5% C 58% |
With ammonium hydroxide; tetraphosphorus decasulfide 1.) 40 h, 140 deg C; Yield given. Multistep reaction. Yields of byproduct given; |
Conditions | Yield |
---|---|
at 150 - 200℃; for 0.5h; further O-alkyl-S-phthalylglycyl xanthates; | A n/a B 53% |
2,2-Dimethyl-1,3-diphenyl-7-thia-2-sila-bicyclo[3.2.0]hept-3-ene-6-thione
A
carbon disulfide
B
1,1-dimethyl-2,5-diphenylsilole
Conditions | Yield |
---|---|
In tetrahydrofuran for 67h; Irradiation; or 180 deg C, 15 h; | A n/a B 40% |
Conditions | Yield |
---|---|
A n/a B 25% |
Conditions | Yield |
---|---|
With sulfur at 270-360°C;; | A 19.8% B n/a |
With sulfur glowing at 500°C; | |
With S glowing at 500°C; |
Conditions | Yield |
---|---|
at 580 - 610℃; for 0.0236111h; Mechanism; Product distribution; pyrolysis of dimethyl sulfide and "disulfide oil", var. reaction conditions; | A 6% B 9.5% C n/a |
Conditions | Yield |
---|---|
With carbon monoxide; platinum | A 1% B n/a |
2,5-diethyl-thiophene
acetyl chloride
A
carbon disulfide
B
1-(2,5-diethyl-[3]thienyl)-ethanone
Conditions | Yield |
---|---|
With aluminium trichloride |
tetrachloromethane
disulfiram
A
carbon disulfide
B
diethylamino-thioxo-methanesulfenyl chloride
Conditions | Yield |
---|---|
at 145℃; |
Conditions | Yield |
---|---|
With aluminium trichloride; sulfur at 120℃; | |
With copper; sulfur | |
With sulfur; aluminium |
2-allylanisole
A
carbon disulfide
B
(2,3-dihydro-2-benzofuranyl)-methyl bromide
Conditions | Yield |
---|---|
With bromine at 0℃; |
4,6-dithioxo-[1,3,5]triazinan-2-one
carbon disulfide
Conditions | Yield |
---|---|
at 360℃; |
thiophosgene
diethyl ether
sodium dimethyldithiocarbamate
A
carbon disulfide
B
bis(dimethylthiocarbamoyl)sulfide
Conditions | Yield |
---|---|
With iron at 100℃; |
Conditions | Yield |
---|---|
With ammonium chloride at 200℃; | |
With aluminium trichloride at 100℃; | |
With iron at 37℃; | |
at 200℃; |
diethyl ether
(dimethyl-thiocarbamic acid )-phthalic acid-thioanhydride
A
carbon disulfide
B
N,N,N',N'-tetramethyl-phthalamide
diethyl ether
tributylphosphine-carbon disulfide adduct
A
carbon disulfide
B
tributylphosphine
Conditions | Yield |
---|---|
With silica gel |
methane
carbon disulfide
Conditions | Yield |
---|---|
With aluminum oxide; silica gel; sulfur at 600℃; | |
With iron sulfide; sulfur at 800 - 1000℃; | |
With silver sulfide; sulfur at 800 - 1000℃; |
ethanol
(dimethyl-thiocarbamic acid )-phthalic acid-thioanhydride
A
carbon disulfide
B
N,N,N',N'-tetramethyl-phthalamide
ethanol
tributylphosphine-carbon disulfide adduct
A
carbon disulfide
B
tributylphosphine
Conditions | Yield |
---|---|
With aluminum oxide; sulfur at 600℃; |
Conditions | Yield |
---|---|
With sulfur |
Conditions | Yield |
---|---|
at 100℃; for 12h; Ionic liquid; Green chemistry; | 100% |
In water at 20℃; for 1h; Green chemistry; | 95% |
In water at 20℃; for 0.833333h; Green chemistry; | 95% |
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.; | 100% |
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; for 1h; Stage #2: With dmap; di-tert-butyl dicarbonate at 0 - 20℃; for 4h; | 96% |
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In methanol at 0 - 5℃; Stage #2: With bis(trichloromethyl) carbonate In chloroform at 0℃; for 4h; Further stages.; | 95% |
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; aniline With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.; | 100% |
Stage #1: carbon disulfide; aniline With potassium carbonate In water at 20℃; for 3h; Inert atmosphere; Stage #2: With 1,3,5-trichloro-2,4,6-triazine In dichloromethane; water at 0℃; for 0.5h; Inert atmosphere; Stage #3: With sodium hydroxide In dichloromethane; water pH=11; Inert atmosphere; | 98% |
Stage #1: carbon disulfide; aniline With potassium carbonate In water at 20℃; Stage #2: With 1,3,5-trichloro-2,4,6-triazine In dichloromethane; water at 0℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
at 100℃; for 12h; Ionic liquid; Green chemistry; | 100% |
aluminum oxide; zinc(II) oxide at 100℃; for 2h; Condensation; | 98% |
In water at 20℃; for 1.33333h; Solvent; Time; Green chemistry; | 97% |
carbon disulfide
methyloxirane
4-methyl-1,3-dithiolane-2-thione
Conditions | Yield |
---|---|
(2-propanolato)-[(2,2',2''-nitrilotris[ethanolato])-(3)-N,O,O',O'']titanium at 120℃; for 48h; | 100% |
With [aluminum((1R,2R)-N,N′-bis(3,5-di-tert-butyl-salicylidene)cyclohexane-1,2-diamine)2O]; tetrabutylammomium bromide at 90℃; for 16h; Neat (no solvent); chemoselective reaction; | 94% |
With potassium hydroxide; ethanol |
carbon disulfide
(S)-1-phenyl-ethylamine
N,N'-bis<(S)-(1-phenylethyl)>thiourea
Conditions | Yield |
---|---|
In ethanol Inert atmosphere; Reflux; | 100% |
at 47℃; | 97% |
In ethanol for 20h; Heating; | 79% |
carbon disulfide
malononitrile
methyl iodide
[Bis(methylthio)methylene]malononitrile
Conditions | Yield |
---|---|
With potassium carbonate; tetrabutylammomium bromide In benzene at 60℃; for 3h; | 100% |
Stage #1: malononitrile With potassium carbonate In dimethyl sulfoxide at 20℃; for 0.166667h; Large scale reaction; Stage #2: carbon disulfide In dimethyl sulfoxide at 0 - 22℃; for 0.5h; Large scale reaction; Stage #3: methyl iodide In dimethyl sulfoxide at 5 - 20℃; Large scale reaction; | 99% |
Stage #1: carbon disulfide; malononitrile With potassium carbonate In dimethyl sulfoxide at 0 - 20℃; for 2h; Stage #2: methyl iodide In dimethyl sulfoxide at 0 - 20℃; for 12h; | 93.9% |
carbon disulfide
cyclohexanol
methyl iodide
<<(methylthio)thiocarbonyl>oxy>cyclohexane
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; cyclohexanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Addition; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; Methylation; Further stages.; | 100% |
Stage #1: carbon disulfide; cyclohexanol In dimethyl sulfoxide at 20℃; for 0.333333h; Stage #2: With N-benzyl-trimethylammonium hydroxide In dimethyl sulfoxide at 20℃; for 1h; Stage #3: methyl iodide In dimethyl sulfoxide at 20℃; for 3h; | 82% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water for 1h; Ambient temperature; | 80% |
carbon disulfide
cyclododecanol
methyl iodide
O-cyclododecyl-S-methyl dithiocarbonate
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; cyclododecanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Addition; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; Methylation; Further stages.; | 100% |
With sodium hydride | 87% |
Stage #1: carbon disulfide; cyclododecanol With n-butyllithium In tetrahydrofuran; hexane at 0 - 20℃; for 3h; Stage #2: methyl iodide at 20℃; | 80% |
piperidine
carbon disulfide
triethylamine
triethylammonium piperidinodithiocarbamate
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 0.2h; | 100% |
In acetonitrile | |
In diethyl ether |
Conditions | Yield |
---|---|
Stage #1: morpholine With sodium hydroxide In methanol; water at 0℃; for 0.333333h; Stage #2: carbon disulfide In methanol; water at 0 - 20℃; | 100% |
With sodium hydroxide In acetonitrile for 5h; | 92% |
With sodium hydroxide In ethanol at 20 - 40℃; | 71% |
carbon disulfide
N-cycloheptatrienylidene-4-methyl-aniline
3-p-Tolyl-3,8a-dihydro-cycloheptathiazole-2-thione
Conditions | Yield |
---|---|
at 60℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With dmap; di-tert-butyl dicarbonate; triethylamine | 100% |
With S,S'-bis(1-phenyl-1H-tetrazol-5-yl) dithiocarbonate; triethylamine In acetonitrile for 0.333333h; | 95% |
Stage #1: carbon disulfide; 1-Adamantanamine With triethylamine In ethanol at 0℃; for 1.5h; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 1h; | 90% |
Stage #1: carbon disulfide; 1-Adamantanamine With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.; | 82% |
With potassium hydroxide |
carbon disulfide
2-[(4-methylphenyl)amino]acetohydrazide
C10H12N3OS2(1-)*K(1+)
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 16h; | 100% |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 16h; | 100% |
carbon disulfide
2-((4-chlorophenyl)amino)acetohydrazide
C9H9ClN3OS2(1-)*K(1+)
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 16h; | 100% |
carbon disulfide
Phenyl-bis-(dimethylamino)-arsin
dimethylthiocarbamic acid phenylarsonous acid-thioanhydride
Conditions | Yield |
---|---|
100% |
carbon disulfide
N-p-bromophenyl-2,4,6-cycloheptatriene-1-imine
3-(4-Bromo-phenyl)-3,8a-dihydro-cycloheptathiazole-2-thione
Conditions | Yield |
---|---|
at 60℃; for 24h; | 100% |
carbon disulfide
N-p-methoxyphenyl-2,4,6-cycloheptatriene-1-imine
3-(4-Methoxy-phenyl)-3,8a-dihydro-cycloheptathiazole-2-thione
Conditions | Yield |
---|---|
at 60℃; for 24h; Mechanism; other p-substituted phenyliminotropones; | 100% |
at 60℃; for 24h; | 100% |
carbon disulfide
bis(N,N-diethylamido)-o-chlorophenylarsonite
C16H24AsClN2S4
Conditions | Yield |
---|---|
100% |
carbon disulfide
C12H26ClP
A
2-(Di-tert-butyl-phosphinothioyl)-3-methyl-but-1-ene-1-thione
B
C12H27ClP(1+)*Cl(1-)
Conditions | Yield |
---|---|
In pentane at 15 - 20℃; for 8h; | A 85% B 100% |
carbon disulfide
2-butylbenzimidazo<1,2-d><1,2,4>thiadiazol-3(2H)-one
3H-benzimidazo<2,1-c><1,2,4>dithiazol-3-thione
Conditions | Yield |
---|---|
In dichloromethane for 24h; Ambient temperature; | 100% |
carbon disulfide
(1S,2R,4R)-1-amino-2-exo-hydroxy-7,7-dimethyl-bicyclo[2.2.1]heptane
(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.01,5>decane
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 15h; Heating; | 100% |
With triethylamine In tetrahydrofuran Heating; |
Conditions | Yield |
---|---|
In diethyl ether for 84h; | 100% |
carbon disulfide
Nicotinic acid hydrazide
potassium N-(pyridine-4-carbonyl)-hydrazine carbodithiolate
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 0 - 20℃; | 100% |
With potassium hydroxide In ethanol for 1h; | 94% |
With potassium hydroxide In ethanol |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol | 100% |
With potassium hydroxide In ethanol at 20℃; | 100% |
With potassium hydroxide In ethanol at 20℃; for 16h; | 99% |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 16h; Cooling with ice; | 100% |
With potassium hydroxide In ethanol at 25℃; for 3h; |
carbon disulfide
2-(2-methyl-1H-indol-3-yl)acetohydrazide
α-(2-Methylindol-3-yl)acetyldithiocarbazinic acid potassium salt
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 10h; Ambient temperature; | 100% |
With potassium hydroxide In ethanol at 20℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With potassium hydroxide In 1,4-dioxane | 100% |
With potassium hydroxide In N,N-dimethyl-formamide at 25℃; for 24h; | |
Stage #1: ethyl acetoacetate With potassium carbonate In N,N-dimethyl-formamide for 1h; Stage #2: carbon disulfide In N,N-dimethyl-formamide for 2h; |
carbon disulfide
4-methoxybenzoic acid hydrazide
potassium N-(4-methoxybenzoyl)hydrazinecarbodithioate
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 20℃; | 100% |
With potassium hydroxide | |
With potassium hydroxide In ethanol |
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