DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:53339-53-0
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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Type:Manufacturers
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Min.Order:1 Gram
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Cas:53339-53-0
Min.Order:100 Gram
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Min.Order:1 Gram
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Min.Order:10 Kilogram
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Type:Trading Company
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Type:Lab/Research institutions
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Min.Order:0 Metric Ton
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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Min.Order:1 Kilogram
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Min.Order:1 Metric Ton
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Min.Order:0
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Type:Lab/Research institutions
inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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FandaChem, a China-based chemical company, specialize in exporting 4-Mercaptobenzyl alcohol / C7H8OS cas no 53339-53-0 (Fandachem), Please contact us by email freely. Appearance:white crystalline powder Storage:Store in dry, dark
Cas:53339-53-0
Min.Order:1 Kilogram
Negotiable
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4-mercaptobenzoic acid
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 6h; Inert atmosphere; | 97% |
With lithium aluminium tetrahydride In tetrahydrofuran for 16.5h; Inert atmosphere; Reflux; | 93% |
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 16h; Inert atmosphere; | 82% |
4-iodo-benzyl alcohol
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Stage #1: 4-iodo-benzyl alcohol With copper(l) iodide; potassium carbonate; sulfur In N,N-dimethyl-formamide at 90℃; for 12h; Inert atmosphere; Stage #2: With sodium tetrahydroborate In N,N-dimethyl-formamide at 40℃; Inert atmosphere; Cooling with ice; | 89% |
4-(pentafluoro-λ6-sulphanyl)benzoic acid
A
[4-(pentafluoro-λ6-sulfanyl)phenyl]methanol
B
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at -5 - 20℃; | A 81% B n/a |
dimethyl 4,4'-dithiobisbenzoate
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran; diethyl ether for 1h; Ambient temperature; | 71% |
diethyl 4,4'-dithiobis
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
4-(methylthio)benzyl alcohol
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
methyl 4-mercaptobenzoate
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
S-(4-carbomethoxyphenyl) N,N-dimethylthiocarbamate
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. KOH / methanol 2: 51 percent / LiAlH4 / tetrahydrofuran / 14 h View Scheme |
4,4'-Dithiobisbenzoic acid
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) SOCl2, 2.) Et3N / 1.) reflux, 2 h, 2.) Et2O, reflux, 2 h 2: 71 percent / LiAlH4 / diethyl ether; tetrahydrofuran / 1 h / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 2: LiAlH4; diethyl ether View Scheme |
4-amino-benzoic acid
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (i) aq. HCl, NaNO2, (ii) potassium ethyl xanthate, (iii) KOH, EtOH 2: HCl 3: LiAlH4 View Scheme |
4-mercaptobenzaldehyde
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; water In acetonitrile |
Conditions | Yield |
---|---|
With N-acetylcystein at 37℃; pH=4.5; Kinetics; pH-value; Reagent/catalyst; |
A
carbon dioxide
B
4-mercaptobenzyl alcohol
D
7-ethyl-10-hydroxycamptothecin
Conditions | Yield |
---|---|
With N-acetylcystein at 37℃; pH=4.5; Kinetics; pH-value; |
Conditions | Yield |
---|---|
With N-acetylcystein at 37℃; pH=4.5; Kinetics; pH-value; |
Conditions | Yield |
---|---|
With N-acetylcystein at 37℃; pH=4.5; Kinetics; pH-value; |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 4 h / 200 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Reflux View Scheme |
N,N-dimethyl[(4-formylphenyl)thio]formamide
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 4h; Reflux; |
4-hydroxy-benzaldehyde
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: 1,4-diaza-bicyclo[2.2.2]octane / N,N-dimethyl-formamide / 0.08 h / 20 °C / Inert atmosphere 1.2: Inert atmosphere 2.1: 4 h / 200 °C 3.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Reflux View Scheme |
Conditions | Yield |
---|---|
With GLUTATHIONE In aq. phosphate buffer for 5h; pH=7.4; |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 12h; | 95% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With water In methanol; chloroform at 0 - 20℃; for 42.1667h; | 94% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
In methanol at 20℃; for 3.08333h; | 94% |
tert-butyl bromoisobutyrate
4-mercaptobenzyl alcohol
tert-butyl 2-(4-hydroxymethylphenylthio)-2-methylpropanoate
Conditions | Yield |
---|---|
Stage #1: 4-mercaptobenzyl alcohol With potassium hydroxide In ethanol for 1h; Reflux; Stage #2: tert-butyl bromoisobutyrate In ethanol for 1.5h; Reflux; | 94% |
4-mercaptobenzyl alcohol
4-mercaptobenzoic acid
Conditions | Yield |
---|---|
With diethylene glycol dimethyl ether at 70℃; for 0.5h; Sonication; | 94% |
With oxygen at 120℃; for 16h; Green chemistry; | 84% |
4-mercaptobenzyl alcohol
bromoacetic acid methyl ester
(4-hydroxymethyl-phenylsulfanyl)-acetic acid methyl ester
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran Heating; | 90% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With sodium methylate In methanol at 15 - 20℃; for 24h; Inert atmosphere; | 85% |
2,2'-dipyridyldisulphide
4-mercaptobenzyl alcohol
(4-(pyridin-2-yldisulfanyl)phenyl)methanol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 83% |
With acetic acid In ethanol at 20℃; for 12h; Inert atmosphere; | 82% |
In dichloromethane at 20℃; | 82% |
2-(isopropyldisulfanyl)pyridine
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With acetic acid In ethanol at 20℃; for 0.5h; | 83% |
With acetic acid In ethanol at 20℃; for 0.5h; | 82% |
4-mercaptobenzyl alcohol
[bromo(difluoro)methyl](trimethyl)silane
Conditions | Yield |
---|---|
Stage #1: 4-mercaptobenzyl alcohol With sodium hydroxide In acetonitrile at 0℃; for 0.166667h; Stage #2: [bromo(difluoro)methyl]-trimethyl-silane In acetonitrile at 0℃; for 0.5h; | 80% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 3h; Inert atmosphere; | 78% |
6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-(prop-2-yn-1-yl)hexanamide
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
In acetonitrile at 20℃; Inert atmosphere; | 78% |
In acetonitrile at 20℃; for 4h; Inert atmosphere; | 43% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 19h; | 76% |
methyl 2-bromomethylbenzoate
4-mercaptobenzyl alcohol
2-(4-hydroxymethyl-phenylsulfanylmethyl)-benzoic acid methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 12h; Heating / reflux; | 72% |
α-bromo-γ-butyrolactone
4-mercaptobenzyl alcohol
3-(4-(hydroxymethyl)phenylthio)dihydrofuran-2(3H)-one
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 72% |
4-mercaptobenzyl alcohol
[bromo(difluoro)methyl](trimethyl)silane
Conditions | Yield |
---|---|
With potassium hydrogen difluoride In dichloromethane; water at 20℃; for 10h; | 72% |
4-mercaptobenzyl alcohol
Conditions | Yield |
---|---|
With N,N,N,N,-tetramethylethylenediamine; tris[2-phenylpyridinato-C2,N]iridium(III) In acetonitrile at 20℃; for 48h; Schlenk technique; Sealed tube; Inert atmosphere; Irradiation; | 71% |
4-mercaptobenzyl alcohol
ethyl bromoacetate
Conditions | Yield |
---|---|
Stage #1: 4-mercaptobenzyl alcohol With potassium carbonate In acetone at 20℃; for 0.5h; Stage #2: ethyl bromoacetate In acetone for 6h; | 70% |
Conditions | Yield |
---|---|
With iodine In ethanol at 0 - 25℃; for 2h; | 69% |
With iodine In ethanol at 0℃; for 2h; | 68.8% |
4-mercaptobenzyl alcohol
4-(hydroxymethyl)phenyl disulfide
Conditions | Yield |
---|---|
With iodine; triethylamine In methanol at 20℃; for 1h; | 66% |
With iodine | |
With iodine |
4-mercaptobenzyl alcohol
ethyl 2-phenyl-2-bromoacetate
1-(4-hydroxymethyl-phenylsulfanyl)-phenyl-acetic acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 12h; Heating / reflux; | 63% |
1-(5-phenyl-1,3,4-oxadiazole-2-carbonyl)-azetidin-3-yl methanesulfonate
4-mercaptobenzyl alcohol
(3-(4-(hydroxymethyl)phenylthio)azetidin-1-yl)(5-phenyl-1,3,4-oxadiazol-2-yl)methanone
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 90℃; | 61% |
With caesium carbonate In N,N-dimethyl-formamide at 90℃; | 61% |
4-mercaptobenzyl alcohol
pyridin-2-yl sulfenyl chloride
(4-(pyridin-2-yldisulfanyl)phenyl)methanol
Conditions | Yield |
---|---|
In dichloromethane | 55% |
4-mercaptobenzyl alcohol
5,5'-dinitro-2,2'-disulfanediyl-bis-pyridine
Conditions | Yield |
---|---|
Stage #1: 4-mercaptobenzyl alcohol; 5,5'-dinitro-2,2'-disulfanediyl-bis-pyridine In dichloromethane at 25℃; for 1.25h; Inert atmosphere; Stage #2: With manganese(IV) oxide In dichloromethane at 25℃; for 0.166667h; Inert atmosphere; | 54.1% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 2.5h; | 47% |
3-nitrophenylsulfenylchloride
4-mercaptobenzyl alcohol
4-<(3-Nitrophenyl)dithio>benzenemethanol
Conditions | Yield |
---|---|
In dichloromethane | 41% |
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