15570-12-4

Basic information

• Product Name: 3-Methoxybenzenethiol
• Synonyms: 3-METHOXYTHIOPHENOL;3-MERCAPTOANISOLE;3-METHOXYBENZENETHIOL;3-METHOXYBENZENTHIOL;M-METHOXYBENZENETHIOL;M-METHOXYTHIOPHENOL;Benzenethiol, 3-methoxy-;m-Methoxy phenyl mercaptan
• CAS NO: 15570-12-4
• Molecular Formula: C₇H₈OS
• Molecular Weight: 140.2
• EINECS: 239-617-7
• Product Categories: THIOL;Sulphur Derivatives;Phenol&Thiophenol&Mercaptan;Phenoles and thiophenoles;API intermediates;Miscellaneous;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds;Thiols/Mercaptans
• Mol File: 15570-12-4.mol
• Article Data: 15

Chemical Properties

• Melting Point: 264.4-268.3 °C (decomp)
• Boiling Point: 223-226 °C(lit.)
• Flash Point: 205 °F
• Appearance: clear colorless to light yellow liquid
• Density: 1.13 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.143mmHg at 25°C
• Refractive Index: n20/D 1.587(lit.)
• Storage Temp.: 2-8°C
• PKA: 6.36±0.10(Predicted)
• Water Solubility: Not miscible or difficult to mix in water. Soluble in methanol, benzene, hexane, toluene and dichloromethane.
• Sensitive: Stench
• BRN: 2041496
• CAS DataBase Reference: 3-Methoxybenzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methoxybenzenethiol(15570-12-4)
• EPA Substance Registry System: 3-Methoxybenzenethiol(15570-12-4)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 20/21/22-36/37/38-22
• Safety Statements: 26-36/37-37/39
• RIDADR: UN 2810 6.1/PG 3
• WGK Germany: 3
• F: 13
• HazardClass: IRRITANT, STENCH
• PackingGroup: III
• Hazardous Substances Data: 15570-12-4(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless to light yellow liquid

Uses

Different sources of media describe the Uses of 15570-12-4 differently. You can refer to the following data:
1. Labelled analogue 3-Methoxy cy as phencyclidine but differs in terms binding affinity. 3-Methoxy
2. 3-Methoxythiophenol is used in the preparation of allenes.

InChI:InChI=1/C7H8OS/c1-8-6-3-2-4-7(9)5-6/h2-5,9H,1H3/p-1

Synthetic route

3-methoxy-1-iodobenzene (766-85-8) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
Stage #1: 3-methoxy-1-iodobenzene 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%
With sodiumsulfide nonahydrate; copper; ethane-1,2-dithiol In dimethyl sulfoxide at 100℃; for 20h; Inert atmosphere; Green chemistry;	89%
With copper(l) iodide; thiourea; L-proline; sodium t-butanolate In dimethyl sulfoxide at 90℃; for 24h; Inert atmosphere;	85%

1-methoxy-3-methylsulfanyl-benzene (2388-74-1) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; diethylamine In xylene for 6h; Heating;	88%

m-Anisidine (536-90-3) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
und ueber mehrere Stufen.Diazotization;
With hydrogenchloride; sodium nitrite Diazotization.man traegt in eine waessr. Loesung von xanthogensaurem Kalium bei 85-90grad ein und verseift den entstandenen Ester durch Kochen mit alkoh. Kalilauge;
(i) aq. NaNO2, aq. HCl, (ii) potassium ethylxanthate, (iii) KOEt, EtOH; Multistep reaction;

methoxybenzene (100-66-3) → 4-Methoxybenzenethiol (696-63-9) + 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With disulfur dichloride; carbon disulfide; aluminium amalgam Destillieren des Reaktionsprodukts unter wenig vermindertem Druck;

1-methoxy-3-methylsulfanyl-benzene (2388-74-1) → 3-methylsulfanylphenol (3463-03-4) + 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With hydrogenchloride; sodium isopropanethiolate 1)sodium isopropanethiolate,HMPA,120 degC,2.5 h 2)hydrochloric acid; Yield given. Multistep reaction. Yields of byproduct given;

[Dimethylamino-(3-methoxy-phenylsulfanyl)-methylene]-dimethyl-ammonium; iodide → 3-methoxybenzenethiol (15570-12-4) + tetramethylurea (632-22-4)

Conditions	Yield
at 20℃; Rate constant; pH=11;

[(3-methoxyphenyl)sulfanyl]acetic acid (3996-32-5) → 3-methoxybenzenethiol (15570-12-4) + Glyoxilic acid (298-12-4)

Conditions	Yield
With perchloric acid; sodium perborate; acetic acid at 24.9℃; Rate constant; Thermodynamic data; Mechanism; var. temp., ΔH(excit.), ΔS(excit.);

Ethyl-3-methoxyphenyl-disulfid (55975-74-1) → 3-methoxybenzenethiol (15570-12-4) + ethanethiol (75-08-1)

Conditions	Yield
With triphenylphosphine In 1,4-dioxane; water at 30℃; Rate constant;

S-(3-methoxyphenyl) dimethylcarbamothioate (50667-88-4) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With potassium hydroxide In methanol Heating;
With sodium hydroxide In methanol

(3S,3aR,4S,6aR,9S,9aR,9bR)-4-Hydroxy-3-(3-methoxy-phenylsulfanylmethyl)-9-methyl-6-methylene-octahydro-azuleno[4,5-b]furan-2,8-dione (248584-43-2) → grosheimin (22489-66-3) + 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With phosphate buffer In methanol at 37℃; pH=7.4; Kinetics; Hydrolysis;

[(3-methoxyphenyl)sulfanyl]acetic acid (3996-32-5) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With perchloric acid; pyridinium chlorochromate In water; acetic acid at 24.85 - 44.85℃; Kinetics; Oxidation;

carbon disulfide (75-15-0) + methoxybenzene (100-66-3) + disulfur dichloride + amalgamated aluminium → 4-Methoxybenzenethiol (696-63-9) + 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
Destillation des entstandenen Oels unter wenig vermindertem Druck;

chloride of/the/ m-anisolesulfonic acid → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With sulfuric acid; zinc

m-anisole-sulfonic acid chloride → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With ethanol; zinc

hydrogenchloride (7647-01-0) + 3-Methoxybenzenesulfonyl chloride (10130-74-2) + zinc → 3-methoxybenzenethiol (15570-12-4)

O-methylresorcine (150-19-6) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
Multi-step reaction with 3 steps 1: (i) NaH, DMF, (ii) /BRN= 635823/ 2: 280 °C 3: aq. NaOH / methanol View Scheme
Multi-step reaction with 3 steps 1: (i) NaH, DMF, (ii) /BRN= 635823/ 2: 270 °C 3: KOH / methanol / Heating View Scheme

O-(3-methoxyphenyl) N,N-dimethylcarbamothioate (50667-83-9) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
Multi-step reaction with 2 steps 1: 280 °C 2: aq. NaOH / methanol View Scheme
Multi-step reaction with 2 steps 1: 270 °C 2: KOH / methanol / Heating View Scheme

((4-methoxy-2-(naphthalen-2-yloxy)phenyl)methylene)bis((3-methoxyphenyl)sulfane) (1221001-36-0) → 9-methoxy-12-(3-methoxyphenylthio)-12H-benzo[a]xanthene (1221001-41-7) + 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With scandium tris(trifluoromethanesulfonate) In dichloromethane at 20℃; Friedel Crafts reaction;

sodium 3-methoxyphenylsulfanesulfonate (1561023-51-5) → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With nickel(II) fluoride; triethoxyphenylsilane; palladium diacetate; trifluoroacetic acid In N,N-dimethyl acetamide at 100℃; Schlenk technique; Inert atmosphere;

C12H17NO2S → 3-methoxybenzenethiol (15570-12-4)

Conditions	Yield
With sodium hydroxide In diphenylether at 80 - 120℃; for 8h; Flow reactor; Large scale;	921.3 g

3-methoxybenzenethiol (15570-12-4) + Bromoacetaldehyde diethyl acetal (2032-35-1) → 1-[(2,2-diethoxyethyl)sulfanyl]-3-methoxybenzene (96803-85-9)

Conditions	Yield
Stage #1: 3-methoxybenzenethiol With potassium carbonate In acetonitrile at 20℃; Stage #2: Bromoacetaldehyde diethyl acetal In acetonitrile for 15h;	100%
With potassium carbonate In acetone at 20℃; for 3h;	100%
With potassium carbonate In acetone at 20℃; for 3h;	100%

3-methoxybenzenethiol (15570-12-4) + methyl iodide (74-88-4) → 1-methoxy-3-methylsulfanyl-benzene (2388-74-1)

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 0.5h;	100%
With sodium hydride In N,N-dimethyl-formamide 1.) 0 deg C, 15 min, 2.) room temperature, 45 min;	90%
With 1,8-diazabicyclo[5.4.0]undec-7-ene In benzene for 48h; Substitution;

5-bromo-3-(2-bromo-4-fluorophenoxy)picolinonitrile (1065609-78-0) + 3-methoxybenzenethiol (15570-12-4) → 5-bromo-3-(2-bromo-4-fluorophenoxy)picolinonitrile

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.5h;	100%

3-methoxybenzenethiol (15570-12-4) + 4,5-dibromothiophene-2-carboxaldehyde (38071-22-6) → 4-bromo-5-[(3-methoxyphenyl)thio]thiophene-2-carbaldehyde (1138032-94-6)

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;

PVS (5535-48-8) + 3-methoxybenzenethiol (15570-12-4) → 2-[(3-methoxyphenyl)sulfanyl]ethyl phenyl sulfone (1308834-07-2)

Conditions	Yield
With potassium carbonate In dichloromethane at 20℃; for 20h; Inert atmosphere;	100%

3-methoxybenzenethiol (15570-12-4) + acetic anhydride (108-24-7) → S-3-methoxyphenyl ethanethioate

Conditions	Yield
Stage #1: 3-methoxybenzenethiol; acetic anhydride With triethylamine In dichloromethane at 20℃; for 3h; Stage #2: With hydrogenchloride In dichloromethane; water	100%

4-butanolide (96-48-0) + 3-methoxybenzenethiol (15570-12-4) → 4-((3-methoxyphenyl)thio)butanoic acid sodium salt

Conditions	Yield
With ethanol; sodium for 24h; Inert atmosphere; Reflux;	100%
With sodium In ethanol for 24h; Inert atmosphere; Reflux;	100%

3-methoxybenzenethiol (15570-12-4) + (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide (206193-17-1) → C19H17F3N2O3S

Conditions	Yield
Stage #1: 3-methoxybenzenethiol With sodium hydride In tetrahydrofuran; mineral oil Stage #2: (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide In tetrahydrofuran; mineral oil at 20℃; for 20h;	100%

3-methoxybenzenethiol (15570-12-4) → bis(3-methoxyphenyl)disulfide (59014-89-0)

Conditions	Yield
1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione In chloroform at 20℃; for 0.0166667h;	99.6%
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione In chloroform at 20℃; for 1h; Inert atmosphere;	97%
With titanium(IV) oxide; oxygen In acetonitrile under 750.075 Torr; for 0.416667h; Irradiation;	96%

3-methoxybenzenethiol (15570-12-4) + 2-fluorobenzonitrile (394-47-8) → 2-((3-methoxyphenyl)thio)benzonitrile

Conditions	Yield
With potassium fluoride on basic alumina; 18-crown-6 ether In acetonitrile for 18h; Heating;	99%
With potassium fluoride on basic alumina; 18-crown-6 ether In acetonitrile for 18h; Heating;	99%

3-methoxybenzenethiol (15570-12-4) + methyl 2-(bromomethyl)-6-nitrobenzoate (61940-21-4) → methyl 2-(3-methoxyphenylthiomethyl)-6-nitrobenzoate

Conditions	Yield
With sodium bicarbonate; sodium chloride; triethylamine In dichloromethane	99%

(1H-1,2,3-benzotriazol-1-yl)(2,3-dihydro-1H-indol-1-yl)methanethione (865075-55-4) + 3-methoxybenzenethiol (15570-12-4) → 2,3-dihydroindole-1-carbodithioic acid 3-methoxyphenyl ester

Conditions	Yield
With sodium hydride In dichloromethane for 18h;	99%

ethyl (2-chloroaceto)acetate (638-07-3) + 3-methoxybenzenethiol (15570-12-4) → 3-methoxybenzenethiol (16768-98-2)

Conditions	Yield
With potassium carbonate In acetonitrile at 0 - 20℃; for 2h;	99%
With potassium hydroxide In methanol at 20℃; for 6h;
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 2.16667h;

3-methoxybenzenethiol (15570-12-4) + 5-bromoacetyl-2,4-dimethylthiazole hydrobromide (76007-16-4) → 1-(2,4-dimethylthiazol-5-yl)-2-(3-methoxyphenylsulfanyl) ethanone (374754-18-4)

Conditions	Yield
With potassium hydroxide In ethanol; water	99%

2-chloro-3-(phenylamino)naphthalene-1,4-dione (1090-16-0) + 3-methoxybenzenethiol (15570-12-4) → 2-(3-methoxyphenylthio)-3-(phenylamino)naphthalene-1,4-dione (1171120-72-1)

Conditions	Yield
With triethylamine In methanol at 70℃; for 4h;	99%
Stage #1: 3-methoxybenzenethiol With triethylamine In water for 0.0833333h; Green chemistry; Stage #2: 2-chloro-3-(phenylamino)naphthalene-1,4-dione In water at 65℃; Green chemistry;	99%

3-methoxybenzenethiol (15570-12-4) + 4-bromo-8-nitroquinolin-2(1H)-one → 4-(3-methoxyphenylthio)-8-nitroquinolin-2(1H)-one

Conditions	Yield
Stage #1: 3-methoxybenzenethiol With sodium hydride In N,N-dimethyl-formamide at 20℃; for 0.5h; Inert atmosphere; Stage #2: 4-bromo-8-nitroquinolin-2(1H)-one In N,N-dimethyl-formamide at 20℃; for 2h; Inert atmosphere;	99%

3-methoxybenzenethiol (15570-12-4) + tert-butyl alcohol (75-65-0) → tert-butyl 3-methoxyphenyl sulfoxide (49833-47-8)

Conditions	Yield
Stage #1: 3-methoxybenzenethiol; tert-butyl alcohol With perchloric acid; acetic anhydride; acetic acid at 20℃; for 24h; Cooling with ice; Stage #2: With dihydrogen peroxide at 0 - 20℃; for 8h;	99%

3-methoxybenzenethiol (15570-12-4) + Diphenylphosphine oxide (4559-70-0) → diphenylthiophosphinic acid-S-3-methoxyphenyl ester

Conditions	Yield
With tert-Butyl peroxybenzoate; potassium iodide In dimethyl sulfoxide at 20℃; for 8h;	99%
With oxygen; rose bengal In N,N-dimethyl-formamide at 20℃; for 12h; Schlenk technique; Inert atmosphere; Irradiation;	91%
With sodium carbonate In N,N-dimethyl-formamide at 20℃; for 3h;	77%

3-methoxybenzenethiol (15570-12-4) + 2,2,6-trimethyl-4-phenyl-1,4-diazabicyclo[4.1.0]heptan-5-one → 3-((3-methoxyphenylthio)methyl)-3,5,5-trimethyl-1-phenylpiperazin-2-one

Conditions	Yield
With tris(pentafluorophenyl)borate In acetonitrile at 65℃; for 18h; Inert atmosphere;	99%

3-methoxybenzenethiol (15570-12-4) + benzenesufonyl hydrazide (80-17-1) → S-(3-methoxyphenyl) benzenesulfonothioate

Conditions	Yield
With tert.-butylhydroperoxide; sodium iodide In acetonitrile at 20℃; for 12h;	99%

3-methoxybenzenethiol (15570-12-4) + tert-butyl (2-oxo-1-propylindolin-3-ylidene)carbamate → tert-butyl (3-((3-methoxyphenyl)thio)-2-oxo-1-propylindolin-3-yl)carbamate

Conditions	Yield
With C12H15CoN2O6(1-)*K(1+) In dichloromethane at 20℃; for 0.0833333h; Schlenk technique; Green chemistry;	99%

1-(4-(4-bromobenzoyl)piperidin-1-yl)ethanone (66309-71-5) + 3-methoxybenzenethiol (15570-12-4) → 1-(4-(4-((3-methoxyphenyl)thio)benzoyl)piperidin-1-yl)ethanone

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); potassium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In toluene at 120℃; for 24h; Sealed tube; Inert atmosphere;	99%

3-methoxybenzenethiol (15570-12-4) + 2-fluoro-6-[(4-methylphenyl)sulfanyl]benzonitrile (175204-11-2) → 2-(3-Methoxy-phenylsulfanyl)-6-p-tolylsulfanyl-benzonitrile

Conditions	Yield
With potassium fluoride on basic alumina; 18-crown-6 ether In acetonitrile for 18h; Heating;	98%

3-methoxybenzenethiol (15570-12-4) + 2-fluoro-6-[(4-methylthio)phenoxy]benzonitrile → 2-(3-Methoxy-phenylsulfanyl)-6-(4-methylsulfanyl-phenoxy)-benzonitrile

Conditions	Yield
With potassium fluoride on basic alumina; 18-crown-6 ether In acetonitrile for 18h; Heating;	98%

3-methoxybenzenethiol (15570-12-4) + 2,6 dichloropurine (5451-40-1) → 2-chloro-6-[(3-methoxyphenyl)thio]purine

Conditions	Yield
With potassium tert-butylate In isopropyl alcohol at 50℃;	98%

3-methoxybenzenethiol (15570-12-4) + 5-(ethoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (15568-86-2) → 5-(3-methoxy-phenylsulfanylmethylene)-2,2-dimethyl-[1,3]dioxane-4,6-dione

Conditions	Yield
With 1-butyl-3-methylimidazolium Tetrafluoroborate In ethyl acetate for 0.1h; microwave irradiation;	98%

3-methoxybenzenethiol (15570-12-4) + 2-(4-fluorophenyl)-6-iodoimidazo[1,2-a]pyridine (478040-44-7) → 2-(4-fluorophenyl)-6-(3-methoxyphenylsulfanyl)imidazo[1,2-a]pyridine

Conditions	Yield
With copper(l) iodide; potassium carbonate; ethylene glycol In isopropyl alcohol at 80℃; for 20h;	98%

2-bromo-pyridine (109-04-6) + 3-methoxybenzenethiol (15570-12-4) → 2-[(3-methoxyphenyl)thio]pyridine

Conditions	Yield
Stage #1: 2-bromo-pyridine With 1,2,3-Benzotriazole; copper(l) iodide In dimethyl sulfoxide for 0.166667h; Stage #2: 3-methoxybenzenethiol With potassium tert-butylate In dimethyl sulfoxide at 100℃; Further stages.;	98%
With potassium carbonate In dimethyl sulfoxide at 110℃; for 18h; Inert atmosphere;	82%
With copper(l) iodide; 1-Hydroxymethyl-1H-benzotriazole; potassium tert-butylate In dimethyl sulfoxide at 80℃;	71%
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 20h;
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 20h;

ethyl 4,7-dichloro-6-fluoroquinoline-3-carboxylate + 3-methoxybenzenethiol (15570-12-4) → C19H15NO3SClF

Conditions	Yield
With triethylamine In tetrahydrofuran at 25℃;	98%
Stage #1: ethyl 4,7-dichloro-6-fluoroquinoline-3-carboxylate; 3-methoxybenzenethiol In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: With potassium carbonate In N,N-dimethyl-formamide at 0 - 10℃; for 1h;	60%

tert-butyl {[5-bromo-4-(2-fluoropyridin-3-yl)-1,3-thiazol-2-yl]methyl}methylcarbamate (1138033-70-1) + 3-methoxybenzenethiol (15570-12-4) → tert-butyl ({4-(2-fluoropyridin-3-yl)-5-[(3-methoxyphenyl)thio]-1,3-thiazol-2-yl}methyl)methylcarbamate (1138033-81-4)

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In toluene at 105℃; for 12h;	98%

Upstream product

• 536-90-3 m-Anisidine 
• 100-66-3 methoxybenzene 
• 2388-74-1 1-methoxy-3-methylsulfanyl-benzene 
• 75-15-0 carbon disulfide 
• 766-85-8 3-methoxy-1-iodobenzene 
• 1221001-36-0 ((4-methoxy-2-(naphthalen-2-yloxy)phenyl)methylene)bis((3-methoxyphenyl)sulfane) 
• 1561023-51-5 sodium S-(3-methoxyphenyl) thiosulfate 
• 50667-83-9 O-(3-methoxyphenyl) N,N-dimethylcarbamothioate 
• 150-19-6 O-methylresorcine 
• 7647-01-0 hydrogenchloride 
• 10130-74-2 m-Methoxybenzenesulfonyl chloride 
• 3996-32-5 [(3-methoxyphenyl)sulfanyl]acetic acid 
• 248584-43-2 (3S,3aR,4S,6aR,9S,9aR,9bR)-4-Hydroxy-3-(3-methoxy-phenylsulfanylmethyl)-9-methyl-6-methylene-octahydro-azuleno[4,5-b]furan-2,8-dione 
• 50667-88-4 S-(3-methoxyphenyl) dimethylcarbamothioate 

Downstream Products

• 91540-76-0 3-(3-methoxy-phenylsulfanyl)-3-(3-nitro-phenyl)-1-phenyl-propan-1-one 
• 873377-73-2 (2-methoxy-phenyl)-(3-methoxy-phenyl)-sulfide 
• 34256-01-4 3-methoxy-benzenesulfonic acid 
• 63762-91-4 2-<(3-Methoxyphenyl)thio>-1-phenylethanone 
• 2388-74-1 1-methoxy-3-methylsulfanyl-benzene 
• 109943-11-5 1-(4-methanesulfonyl-phenylsulfanyl)-3-methoxy-benzene 
• 92243-62-4 Ethyl-(3-methoxy-phenyl)-trithiocarbonat 
• 100376-34-9 2-(3-Methoxy-3,6-dichlor-phenylmercapto)-cyclohexandion-(1,3) 
• 128348-23-2 3-methoxyphenyl 3-thienyl sulfide 
• 98733-08-5 1-<(2,2-dimethoxyethyl)thio>-3-methoxybenzene 
• 76440-44-3 3-((m-methoxyphenyl)thio)cyclohexanone 
• 76440-44-3 3-((m-methoxyphenyl)thio)cyclohexanone 
• 64793-83-5 3-(3-Methoxy-phenylthio)-isovaleriansaeure 
• 81536-25-6 ethyl 2-mercapto-4-methoxycinnamate 

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