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:100-53-8
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:100-53-8
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryHangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical,
Cas:100-53-8
Min.Order:1 Gram
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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
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:100-53-8
Min.Order:10 Gram
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:100-53-8
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Benzyl MercaptanAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
stable supply&competitive price Storage:Available Package:25KG Or as client requirement Application:Important pharm intermediate Transportation:By air or By sea
Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
FandaChem, a China-based chemical company, specialize in exporting Benzyl mercaptan / C7H8S cas 100-53-8 (Fandachem), Please contact us by email freely. Appearance:white crystalline powder Storage:Store in dry, dark and ventilated pla
Cas:100-53-8
Min.Order:1 Kilogram
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inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:100-53-8
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Xiamen Luyunjia Trading Co.,Ltd Package:1kg/bag; 1781kg/drum, or as customer's request. Application:Xiamen Luyunjia Trading Co.,Ltd Transportation:DHL, EMS, FedEx, TNT, AIR, SEA Port:Beijing,Shanghai,Guangzhou ,China main port
Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Prompt reaction, good quality and best service make us reliable and outstanding in this industry.Appearance:Colorless to light yellow l
Cas:100-53-8
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
in storeAppearance:Colorless to light yellow transparent liquid Package:1kg Application:Organic Chemicals
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:100-53-8
Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiry1.We are not just a manufacturer but aslo a trading company.Our office located in Hangzhou. 2.We have document department who can meet customers' documentary requirements. 3.We have many cooperative plants who can provide price support for
Benzyl mercaptan Basic information Product Name: Benzyl mercaptan Synonyms: A-TOLUENETHIOL;BENZYL MERCAPTAN;Benzenemethanethiol;FEMA 2147;ALPHA-TOLUENETHIOL;ALPHA-T
Cas:100-53-8
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryConditions | Yield |
---|---|
With hydrosulfide exchange resin In acetonitrile at 25℃; for 0.25h; | 98% |
With thiourea In ethanol for 0.166667h; Reflux; | 95% |
With hydrosulfide exchange resin (from Amberlite IRA-400); triethylamine hydrochloride In methanol for 1h; Ambient temperature; | 87% |
Conditions | Yield |
---|---|
With sodium hydrogen telluride In ethanol 1.) 0 deg C, 2.) 40 deg C, 30 min; | 97% |
With sodium hydrogen telluride In ethanol Product distribution; 1.) 0 deg C, 2.) 40 deg C, 30 min; reductive cleavage of sulfur-sulfur bonds in dialkyl, diaryl disulfides and organic thiosulfites; | 97% |
With triethylphosphine In tetrahydrofuran; water for 1h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at 22 - 25℃; for 0.5h; | 97% |
Conditions | Yield |
---|---|
Stage #1: benzyl bromide With potassium carbonate; tiolacetic acid In methanol at 20℃; for 0.5h; Stage #2: With potassium carbonate In methanol at 20℃; for 0.5h; | 96% |
With hydrosulfide exchange resin (from Amberlite IRA-400); triethylamine hydrochloride In methanol for 1h; Ambient temperature; | 88% |
Stage #1: benzyl bromide With thiourea In water at 100℃; for 2h; Inert atmosphere; Stage #2: With sodium hydroxide In water; toluene at 60℃; for 1h; | 84% |
benzylthioacetate
phenylmethanethiol
Conditions | Yield |
---|---|
With acetyl chloride In methanol at 25 - 30℃; for 3h; | 96% |
With potassium carbonate In methanol at 20℃; for 0.5h; | 96% |
With palladium diacetate In methanol for 1h; Heating; | 95% |
Thiocarbonic acid S-benzyl ester O-[1-(3,5-dimethoxy-phenyl)-2-oxo-2-phenyl-ethyl] ester
phenylmethanethiol
Conditions | Yield |
---|---|
In benzene for 1h; Irradiation; | 95% |
1-[[(Z)-2-(benzylsulfanyl)vinyl]sulfonyl]-4-methylbenzene
phenylmethanethiol
Conditions | Yield |
---|---|
With pyrrolidine In acetonitrile at 20℃; | 95% |
Conditions | Yield |
---|---|
With hydrogen In water at 180℃; under 7500.75 Torr; for 5h; Reagent/catalyst; Temperature; Autoclave; | A 95% B 12% |
Conditions | Yield |
---|---|
In water at 70℃; for 2h; | A 94.27% B n/a |
at 70℃; for 2h; |
1-(2-Benzylsulfanyl-2-methyl-propane-1-sulfonyl)-4-methyl-benzene
phenylmethanethiol
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol for 0.5h; Product distribution; Ambient temperature; further reagents: CH3ONa, CH3OLi, KOH, other solvent: CH3OH; cleavage of various adducts; | 93% |
N-Phenyl-thioformimidic acid benzyl ester
phenylmethanethiol
Conditions | Yield |
---|---|
With hydrogenchloride In water Ambient temperature; | 92% |
Conditions | Yield |
---|---|
With magnesium; acetic acid In methanol at 20℃; | 92% |
phenylmethanethiol
Conditions | Yield |
---|---|
Stage #1: C22H18O3S With sodium hypochlorite In dichloromethane; water at 20℃; Stage #2: at 80℃; for 12h; | 90% |
Conditions | Yield |
---|---|
With sodium hydrogen telluride In ethanol 1.) 0 deg C, 2.) 40 deg C, 30 min; | 89% |
Conditions | Yield |
---|---|
In chloroform 1:1 mixt. stirred for 10 min; evapd., washed (Et2O), dried (vac.); NMR; | A 89% B n/a |
trimethyl(4-mercaptomethylphenyl)silane
phenylmethanethiol
Conditions | Yield |
---|---|
With potassium trimethylsilonate In dimethyl sulfoxide at 60℃; under 760.051 Torr; for 12h; Catalytic behavior; Reagent/catalyst; Solvent; Sealed tube; | 88% |
Conditions | Yield |
---|---|
With potassium carbonate; tiolacetic acid In methanol at 20℃; for 0.5h; | A 87% B 13% |
dibenzyl trithiocarbonate
phenylmethanethiol
Conditions | Yield |
---|---|
With diisobutylaluminium hydride In toluene at 110℃; | 86% |
Conditions | Yield |
---|---|
With tetraphosphorus decasulfide In toluene for 1.5h; Solvent; Reagent/catalyst; Reflux; | 85% |
With diethyl ether; ethylmagnesium bromide | |
With diethyl ether; phenylmagnesium bromide |
Conditions | Yield |
---|---|
Stage #1: benzyl alcohol With sodium sulfide; sodium hydrogencarbonate In ethanol for 2h; Reflux; Enzymatic reaction; Stage #2: With hydrogenchloride In ethanol; water Reagent/catalyst; | 85% |
Stage #1: benzyl alcohol With N-Bromosuccinimide; triphenylphosphine In acetone at -10 - 25℃; Substitution; Stage #2: With polymer supported hydrosulfide resin In acetone at 25℃; for 0.166667h; Substitution; | 81% |
With Lawessons reagent In toluene for 48h; Heating; | 55% |
methanol
benzyl dithiobenzoate
A
methyl thiobenzoate
B
phenylmethanethiol
Conditions | Yield |
---|---|
With sodium hydroxide In water at 20℃; for 1h; | A 82% B n/a |
S-benzyl thiocarbamate
phenylmethanethiol
Conditions | Yield |
---|---|
Stage #1: benzyl S-thiocarbamate With tetraphosphorus decasulfide In toluene Reflux; Stage #2: With water Acidic conditions; | 80% |
allyl(benzyl)sulfide
A
1-benzylsulfanyl-3-chloro-propan-2-ol
B
phenylmethanethiol
Conditions | Yield |
---|---|
With water; copper dichloride; lithium tetrachloropalladate(II) In N,N-dimethyl-formamide at 50℃; for 24h; | A 78.7% B 10% |
SS-benzyl O-methyl carbono(dithioperoxoate)
A
methyl α-(phenylthio)acetate
B
phenylmethanethiol
Conditions | Yield |
---|---|
With triphenylphosphine In benzene Ambient temperature; | A 78% B 21% |
Conditions | Yield |
---|---|
With tetraphosphorus decasulfide In toluene for 3h; Solvent; Reflux; | 75% |
Benzylsulfanyl-triisopropyl-silane
A
triisopropylsilyl fluoride
B
phenylmethanethiol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride; water In tetrahydrofuran 1.) 25 deg C, 1 h; | A n/a B 73% |
benzyl 2-methylprop-2-en-1-yl sulfide
A
phenylmethanethiol
Conditions | Yield |
---|---|
With water; copper dichloride; lithium tetrachloropalladate(II) In N,N-dimethyl-formamide at 50℃; for 48h; | A 10% B 72.6% |
O,S-dibenzyl dithiocarbonate
A
dibenzyl sulfide
B
dithiocarbonic acid S,S'-dibenzyl ester
C
phenylmethanethiol
Conditions | Yield |
---|---|
Aliquat 336 at 100℃; for 1.5h; Yields of byproduct given; | A n/a B 70% C n/a |
Conditions | Yield |
---|---|
In water; acetic acid electroreduction on Hg-cathode, 0.8 A; | A 70% B 13% |
Conditions | Yield |
---|---|
Stage #1: acetic anhydride With molybdenium(VI) dioxodichloride In dichloromethane at 20℃; for 0.5h; Stage #2: phenylmethanethiol In dichloromethane at 20℃; for 4h; | 100% |
With silica gel for 0.0533333h; Microwave irradiation; neat (no solvent); | 100% |
yttria-stabilized zirconia In acetonitrile for 6h; Heating; | 97% |
Conditions | Yield |
---|---|
With pyridine chromium peroxide for 0.02h; Product distribution; effect of various chromium(VI) based oxidants; | 100% |
With barium ferrate(VI) In benzene for 1h; Product distribution; Heating; | 100% |
With pyridine chromium peroxide for 0.02h; | 100% |
nitromethane
cyclohexanone
phenylmethanethiol
1-benzylthio-1-nitromethylcyclohexane
Conditions | Yield |
---|---|
With piperidine In benzene | 100% |
With piperidine In acetonitrile for 4h; Heating; | 96% |
With piperidine In acetonitrile for 4h; Heating / reflux; | 22% |
With piperidine In benzene Heating; |
nitromethane
cyclopentanone
phenylmethanethiol
1-benzylthio-1-nitromethylcyclopentane
Conditions | Yield |
---|---|
With piperidine In benzene | 100% |
With piperidine In acetonitrile for 4h; Heating; | 94% |
With piperidine In benzene Heating; |
(2-nitroethenyl)benzene
phenylmethanethiol
benzyl (2-nitro-1-phenylethyl) sulfide
Conditions | Yield |
---|---|
at 20℃; for 0.1h; Michael addition; neat (no solvent); | 100% |
at 20℃; for 2h; Michael addition; Neat (no solvent); regioselective reaction; | 92% |
In water at 20℃; for 1h; thia-Michael addition; | 91% |
With 2,2'-azobis(isobutyronitrile); quinoclamine; N,N-dimethyl-formamide; Quinine In toluene |
styrene oxide
phenylmethanethiol
1-(1-phenyl-2-hydroxy) ethyl-benzyl sulfide
Conditions | Yield |
---|---|
With erbium(III) triflate In acetonitrile at 25℃; for 0.75h; | 100% |
aluminum oxide; molybdenum(VI) oxide at 20℃; for 0.25h; | 89% |
ammonium cerium(IV) nitrate In acetonitrile for 1.5h; Heating; | 70% |
With 2C21H12N3O6(3-)*Co(3+)*17H2O*Tb(3+) In neat (no solvent) at 25℃; for 4h; Reagent/catalyst; regioselective reaction; | 86 %Chromat. |
2-benzofuran-1(3H)-one
phenylmethanethiol
2-<(Benzylthio)methyl>benzoic acid
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide; mineral oil for 45h; Reflux; | 100% |
With sodium hydride In N,N-dimethyl-formamide for 24h; Heating; | 99% |
58% | |
With sodium ethanolate In ethanol |
Conditions | Yield |
---|---|
Stage #1: phenylmethanethiol With potassium hydroxide In methanol at 70℃; for 0.25h; Inert atmosphere; Schlenk technique; Green chemistry; Stage #2: benzyl bromide With copper(l) iodide In methanol at 110℃; for 12h; Inert atmosphere; Schlenk technique; Green chemistry; | 100% |
Stage #1: phenylmethanethiol With sodium methylate In methanol at -10℃; for 0.166667h; Stage #2: benzyl bromide In methanol at 20℃; | 96% |
Stage #1: phenylmethanethiol With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere; Stage #2: benzyl bromide In tetrahydrofuran at 20℃; for 4h; Inert atmosphere; | 92% |
1,3-dibromoroacetone
phenylmethanethiol
1,3-Bis<(phenylmethyl)thio>-2-propanone
Conditions | Yield |
---|---|
With sodium In ethanol at -5℃; for 4h; | 100% |
Conditions | Yield |
---|---|
With pyridine; O-phenyl phosphorodichloridate In 1,2-dimethoxyethane for 16h; Ambient temperature; | 100% |
(methoxycarbonyl)disulfanyl chloride
phenylmethanethiol
Methoxycarbonyl benzyl trisulfane
Conditions | Yield |
---|---|
In dichloromethane at -78℃; for 1h; | 100% |
Conditions | Yield |
---|---|
With pyridine In diethyl ether for 0.5h; | 100% |
methyl (((9H-fluoren-9-yl)methoxy)carbonyl)-L-phenylalaninate
phenylmethanethiol
A
methyl (2S)-2-amino-3-phenylpropanoate
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In N,N-dimethyl-formamide for 0.0333333h; Product distribution; other protected peptides, other thiol, var. TBAF conc., var. time, var. solvent, with or without ultrasound mixing; | A n/a B 100% |
With tetrabutyl ammonium fluoride In N,N-dimethyl-formamide for 0.05h; | A n/a B 100% |
vinylidene-1,1-diphosphonic acid
phenylmethanethiol
(2-Benzylsulfanyl-1-phosphono-ethyl)-phosphonic acid
Conditions | Yield |
---|---|
With acetic acid; triethylamine at 110℃; for 15h; Product distribution; reaction of vinylidenediphosphonic acid with various thiols; | 100% |
With acetic acid; triethylamine at 110℃; for 15h; | 100% |
nitromethane
phenylmethanethiol
acetone
benzyl(2-methyl-1-nitropropan-2-yl)sulfane
Conditions | Yield |
---|---|
With piperidine In benzene | 100% |
With piperidine In tetrahydrofuran for 12h; Heating; | 96% |
With piperidine for 15h; Heating; | 49% |
In benzene at 100℃; for 22h; Dean-Stark; | 23% |
With piperidine In benzene for 10h; Reflux; Inert atmosphere; |
phenylmethanethiol
Benzylthiosulfenylchlorid
Conditions | Yield |
---|---|
With pyridine; sulfur dichloride In diethyl ether at -78℃; for 0.5h; | 100% |
Conditions | Yield |
---|---|
With benzyl alcohol; aluminium dodecatungsten phosphate In dichloromethane at 20℃; for 4h; | 100% |
With methanesulfonic acid at 80℃; for 0.0833333h; Microwave irradiation; Ionic liquid; | 99% |
With boron trifluoride diethyl etherate In dichloromethane at 20℃; for 0.0166667h; | 99% |
With toluene-4-sulfonic acid In acetonitrile for 12h; Reflux; | 97% |
With toluene-4-sulfonic acid In benzene |
Conditions | Yield |
---|---|
With sodium carbonate In methanol; water at 20℃; for 0.5h; | 100% |
With sodium ethanolate In ethanol for 0.166667h; Reflux; Inert atmosphere; | 99% |
With potassium carbonate In acetonitrile for 3h; Inert atmosphere; | 95% |
phenylmethanethiol
[(3aR,5S,6aR)-5-Azidomethyl-2,2-dimethyl-dihydro-furo[2,3-d][1,3]dioxol-(6Z)-ylidene]-acetic acid methyl ester
Conditions | Yield |
---|---|
With lithium methanolate In methanol for 0.0833333h; | 100% |
phenylmethanethiol
acetic acid 3-acetoxy-6-acetoxymethyl-2-(4,5-diacetoxy-2-acetoxymethyl-6-but-3-enyloxy-tetrahydro-pyran-3-yloxy)-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In 1,4-dioxane at 50 - 80℃; Addition; | 100% |
phenylmethanethiol
N,N-dimethyl-5,7-bis(trifluoroacetyl)-8-quinolylamine
1-[8-Benzylsulfanyl-5-(2,2,2-trifluoro-acetyl)-quinolin-7-yl]-2,2,2-trifluoro-ethanone
Conditions | Yield |
---|---|
In acetonitrile for 8h; Substitution; Heating; | 100% |
2-iodo-4-methoxybromobenzene
phenylmethanethiol
2-benzylsulfanyl-1-bromo-4-methoxy-benzene
Conditions | Yield |
---|---|
With triethylamine; 1,1'-bis-(diphenylphosphino)ferrocene; bis(dibenzylideneacetone)-palladium(0) In N,N-dimethyl-formamide at 70℃; for 2.5h; | 100% |
With 1,1'-bis-(diphenylphosphino)ferrocene; triethylamine; bis(dibenzylideneacetone)-palladium(0) In N,N-dimethyl-formamide at 70℃; for 3h; |
Conditions | Yield |
---|---|
With potassium hydroxide; N-benzyl-N,N,N-triethylammonium chloride at 20℃; for 1h; | 100% |
nitromethane
phenylmethanethiol
butanone
2-benzylthio-2-nitromethylbutane
Conditions | Yield |
---|---|
With piperidine In benzene | 100% |
With ethylenediamine In acetonitrile for 8h; Heating; | 95% |
With ethylenediamine In acetonitrile |
nitromethane
phenylmethanethiol
cycloheptanone
1-benzylthio-1-nitromethylcycloheptane
Conditions | Yield |
---|---|
With piperidine In benzene | 100% |
With ethylenediamine In acetonitrile for 12h; Heating; | 83% |
ethyl 3-methylbut-2-enoate
phenylmethanethiol
ethyl 3-methyl-3-benzylthiobutanoate
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol at 20 - 50℃; for 36h; | 100% |
phenylmethanethiol
(4-bromo-phenyl)-(2-fluoro-4-methoxy-phenyl)-methanone
(2-benzylsulfanyl-4-methoxyphenyl)(4-bromophenyl)methanone
Conditions | Yield |
---|---|
Stage #1: phenylmethanethiol With potassium tert-butylate In tetrahydrofuran at 20℃; for 0.5h; Stage #2: (4-bromo-phenyl)-(2-fluoro-4-methoxy-phenyl)-methanone In tetrahydrofuran at 20℃; for 1.5h; | 100% |
With potassium tert-butylate In tetrahydrofuran at 20℃; |
ethynyl p-tolyl sulfone
phenylmethanethiol
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 0.333333h; | 100% |
phenylmethanethiol
(4R,5aS,7aS,7bR)-5,5a,6,7,7a,7b-hexahydro-7b-hydroxy-4-methyl-indeno[1,7-bc]furan-2(4H)-one
Conditions | Yield |
---|---|
In ethanol at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
Stage #1: phenylmethanethiol With tetra-(n-butyl)ammonium iodide; caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 1-iodo-propane In N,N-dimethyl-formamide at 0 - 20℃; for 2h; | 100% |
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