1-methoxy-2-methyl-4-(methylthio)benzene
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With potassium permanganate; potassium carbonate |
2-methoxy-5-(methylthio)benzoic acid
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With potassium permanganate; potassium carbonate |
5-chlorosulfonyl-2-anisic acid
chloroacetic acid
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; sodium hydrogencarbonate; sodium sulfite 1) H2O, 75 deg C, 1 h, 2) 105 deg C, 47 h; Yield given. Multistep reaction; |
1-methoxy-2-methyl-4-(methylthio)benzene
2-methoxy-5-methylsulphonylbenzoic acid
4-methoxy-3-methylbenzenethiol
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aqueous NaOH 2: potassium carbonate; aqueous potassium permanganate solution View Scheme |
5-chlorosulfonyl-2-anisic acid
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tin; aqueous hydrochloric acid 2: aq. NaOH solution 3: potassium carbonate; aqueous potassium permanganate solution View Scheme |
5-mercapto-2-methoxybenzoic acid
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. NaOH solution 2: potassium carbonate; aqueous potassium permanganate solution View Scheme |
4-methoxy-3-methylbenzene-1-sulfonyl chloride
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tin; aqueous HCl / zuletzt auf dem Dampfbad 2: aqueous NaOH 3: potassium carbonate; aqueous potassium permanganate solution View Scheme |
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With hydrogenchloride | |
With hydrogenchloride | |
With hydrogenchloride | |
With hydrogenchloride |
2-methoxy-5-methylsulphonylbenzoic acid
(E)-methyl 4-aminobut-2-enoate trifluoroacetic acid salt
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; Sealed tube; | 74% |
2-methoxy-5-methylsulphonylbenzoic acid
chloroformic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In N-methyl-acetamide | 70% |
2-methoxy-5-methylsulphonylbenzoic acid
3-fluoro-4-[4-(5-methanesulfonyl-2-methoxy-benzoyl)-piperazin-1-yl]-benzonitrile
Conditions | Yield |
---|---|
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 69% |
2-methoxy-5-methylsulphonylbenzoic acid
chloroformic acid ethyl ester
C12H14O7S
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -40 - -10℃; for 0.5h; |
2-methoxy-5-methylsulphonylbenzoic acid
N-[2-(N'-benzyl-N'-methylamino)ethyl]-6-methoxy-3-methylsulfonylbenzamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / CH2Cl2 / 0.5 h / -40 - -10 °C 2: CH2Cl2 / 2 h / Ambient temperature View Scheme |
3-(pyridin-2-yl)-1H-pyrazol-4-amine
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With 1-hydroxy-7-aza-benzotriazole; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In N,N-dimethyl-formamide at 20℃; for 2h; |
3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepan-1-yl)ethyl)-3-phenylpyrrolidine hydrochloric acid salt
(+)-3-phenyl-3-(2-hydroxy-ethyl)-pyrrolidine (R,R)-di-p-anisoyltartaric acid salt
2-methoxy-5-methylsulphonylbenzoic acid
2-methoxy-5-methylsulphonylbenzoic acid
chloroformic acid ethyl ester
4-Amino-1,2-diethyl-pyrazolidine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 1.03 g (29%) |
2-methoxy-5-methylsulphonylbenzoic acid
isobutyl chloroformate
Conditions | Yield |
---|---|
With hydrogenchloride; triethylamine In water; ethyl acetate; isopropyl alcohol; acetone |
1,4-dioxane
2-methoxy-5-methylsulphonylbenzoic acid
N,N-diethylethylenediamine
tiapride
Conditions | Yield |
---|---|
In water |
2-methoxy-5-methylsulphonylbenzoic acid
N-benzyl-N-methylethylenediamine
N-[2-(N'-benzyl-N'-methylamino)ethyl]-6-methoxy-3-methylsulfonylbenzamide
3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepan-1-yl)ethyl)-3-phenylpyrrolidine hydrochloric acid salt
2-methoxy-5-methylsulphonylbenzoic acid
(+)-3-phenyl-3-(2-hydroxy-ethyl)-pyrrolidine (R,R)-di-p-anisoyltartaric acid salt
2-methoxy-5-methylsulphonylbenzoic acid
2-methoxy-5-methylsulphonylbenzoic acid
C2HF3O2*C15H24N2O4S3
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / water; N,N-dimethyl-formamide 2: tris-(2-carboxyethyl)-phosphine hydrochloride; triethylamine / water; N,N-dimethyl-formamide View Scheme |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In water; N,N-dimethyl-formamide |
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: borane-THF / tetrahydrofuran / 16 h / 0 °C 2: phosphorus tribromide / dichloromethane / 18 h / 20 °C 3: potassium carbonate / acetonitrile / 100 °C View Scheme |
2-methoxy-5-methylsulphonylbenzoic acid
2-(bromomethyl)-1-methoxy-4-(methylsulfonyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: borane-THF / tetrahydrofuran / 16 h / 0 °C 2: phosphorus tribromide / dichloromethane / 18 h / 20 °C View Scheme |
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
With borane-THF In tetrahydrofuran at 0℃; for 16h; | 4.9 g |
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: thionyl chloride / 3 h / Reflux; Inert atmosphere 2: triethylamine / dichloromethane / 20 °C 3: hydrogenchloride / acetone; water / 5 h / Reflux 4: Burgess Reagent / tetrahydrofuran / 0.17 h / 70 °C / Microwave irradiation View Scheme |
2-methoxy-5-methylsulphonylbenzoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: thionyl chloride / 3 h / Reflux; Inert atmosphere 2: triethylamine / dichloromethane / 20 °C 3: hydrogenchloride / acetone; water / 5 h / Reflux 4: Burgess Reagent / tetrahydrofuran / 0.17 h / 70 °C / Microwave irradiation 5: boron tribromide / dichloromethane / 0 - 20 °C View Scheme |
The Molecular formula of 2-methoxyl-5-methysulfonyl benzoic acid(50390-76-6):C9H10O5S
The Molecular Weight of 2-methoxyl-5-methysulfonyl benzoic acid(50390-76-6):230.24
The Molecular Structure of 2-Methyl-1,3-cyclopentanedione(765-69-5) is:
Melting point:189-197°C
Appearance:white to off-white powder
Synonyms:5-METHANESULFONYL-2-METHOXY-BENZOIC ACID;2-Methoxy-5-(methylsulphonyl)benzoic acid;2-METHOXY-5-METHYL SULFONYLBENZOIC ACID;4-methox+c578y-3-carboxymethylbenzenesulponate;5-mesyl-o-anisic acid;2-methoxyl-5-methysulfonyl benzoic acid;2-Methoxy-5-methy1 sulfonylbenzoic acid;2-METHOXY-6-(METHYLSULPHONYL)BENZOIC ACID
Hazard Codes
Xi:Irritant
Hazard Note:Irritant
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View