GL Biochem (Shanghai) Ltd. founded in 1998, has become an internationally recognized biochemical manufacturing company that specializes in producing/synthesizing and providing peptide reagents, custom peptides and antibodies. GL Biochem is based in
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inquiryIn stock Contract customization Low Temperature Reactions Fluorine Chemistry Hydrogenation Nitration Chlorination Appearance:white to light yellow crystalline powder Storage:cool and dry warehouse Package:25KG/Drum Application:pharmaceutical i
Hunan Kaimir Biotechnology Co., Ltd. is a professional technology company specializing in the research and production of raw materials and intermediates. In 2017, it was recognized as a high-tech enterprise and a small technological innovation giant
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inquiryProduct Description Product website: http://www.finerchem.com Product Name ISOPSEUDOCUMENOL CAS No. 697-82-5 Appearance
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inquiryBest service,high quality and cheap price. Appearance: Clear colorless to light yellow liquid Storage:Dry,Seal and Cool place Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air
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2,3,5-Trimethylphenol Factory CAS 697-82-5 Isopseudocumenol CAS no 697-82-5 1-Hydroxy-2,3,5-trimethylbenzene 2,3,5-Trimethylphenol Manufacturer High quality Best price In stock factory CAS 697-82-5 2,3,5-Trimethylphenol COA TDS price MSDS
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inquiryName:2,3,5-Trimethylphenol CAS NO: 697-82-5 Grade:Medical scientific research and export Molecular formula:C9H12O Molecular weight:136.191 Product Quality 12 years of chemical raw materials Mature operation of the industry System stability
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inquiryProduct Name: 2,3,5-Trimethylphenol Synonyms: ISOPSEUDOCUMENOL;AKOS BBS-00008093;6-HYDROXYPSEUDOCUMENE;2,3,5-TRIMETHYLPHENOL;1-Hydroxy-2,3,5-trimethylbenzene;2,3,5-trimethyl-pheno;2,3,5-Thrimethylphenol;2,3,5-Trimethylphenol/TMP/Isopse
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inquiryName: 2,3,5-Trimethylphenol Synonyms: Isopseudocumenol CAS:697-82-5 MF: C9H12O Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application: Flavours & Fragrances Intermediates Transportation:B
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inquiryProduct Name: 2,3,5-Trimethylphenol Synonyms: ISOPSEUDOCUMENOL;AKOS BBS-00008093;6-HYDROXYPSEUDOCUMENE;2,3,5-TRIMETHYLPHENOL;1-Hydroxy-2,3,5-trimethylbenzene;2,3,5-trimethyl-pheno;2,3,5-TRIMETHYLPHENOL PESTANAL, 250 MG;2,3,5-Trimethylphenol, 98
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inquiry2,3,5-Trimethylphenol CAS:697-82-5 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inter
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Name: 2, 3, 5-Trimethylphenol CAS NO.: 697-82-5 Structural formula: Appearance: almost white solid, melting point: 92~94℃ Content: 99.0% mi
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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inquiry2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With indium; ammonium chloride In ethanol for 18h; Debenzylation; Heating; | 100% |
With indium; ammonium chloride In methanol for 18h; Heating; | 100% |
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With tetrahydrofuran; titanium(III) chloride; lithium for 14h; Heating; | 92% |
2,3,5-Trimethyl-(4-methylphenylsulfonyloxy)benzene
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With titanium(III) chloride; lithium In tetrahydrofuran at 25℃; for 18h; Substitution; | 91% |
2,4,6-trimethylpyrylium tetrafluoroborate
dimethylsulfoxonium methylide
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
In tetrahydrofuran; dimethyl sulfoxide 1.) -5 deg C, 1 h, 2.) room temperature, 7 h; | 80% |
methanol
2,3-Dimethylphenol
A
2,3,6-trimethylphenol
B
2,3,4-trimethylphenol
C
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
Pd-containing mordenite at 350℃; | A 80% B 5% C 5% |
methanol
3,5-Dimethylphenol
A
3,4,5-trimethylphenol
B
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
Pd-containing mordenite at 350℃; | A 6% B 70% |
1,2,4-Trimethylbenzene
A
2,4-dimethylbenzyl alcohol
B
Trimethylhydroquinone
C
2,4,5-trimethylphenol
D
2,3,6-trimethylphenol
E
2,3,5-trimethylphenol
F
2,5-dimethylbenzyl alcohol
Conditions | Yield |
---|---|
With glucose dehydrogenase; D-glucose; P450 BM3 R47S, Y51W, A330F, I401M mutant; NADPH; catalase; ascorbic acid In aq. phosphate buffer; dimethyl sulfoxide pH=7.5; Catalytic behavior; Enzymatic reaction; | A 25% B 23% C 28% D 5% E 8% F 9% |
formaldehyd
3,5-dimethyl-2-cyclohexen-1-one
diethyl amine hydrochloride
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With hydrogenchloride; ethanol Behandeln des Reaktionsprodukts mit HCl in Aether und Erhitzen der erhaltenen Hydrochloride unter vermindertem Druck auf 200-235grad; |
3,5,5-Trimethylcyclohex-2-en-1-one
A
3,4,5-trimethylphenol
B
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With bromine; 1,2,4-Trichlorobenzene |
3,5-dimethyl-2-piperidin-1-ylmethyl-phenol
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With calcium hydroxide | |
With 1,4-dioxane; copper oxide-chromium oxide at 165℃; Hydrogenolyse; |
2-(Morpholinomethyl)-3,5-dimethylphenol
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With 1,4-dioxane; copper oxide-chromium oxide at 165℃; Hydrogenolyse; |
Conditions | Yield |
---|---|
With aluminium trichloride at 100℃; |
Conditions | Yield |
---|---|
With aluminium trichloride at 100℃; |
2-chloro-3,5,6-trimethylphenol
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With sodium hydroxide; aluminum nickel |
Conditions | Yield |
---|---|
Diazotization; | |
With sulfuric acid; sodium nitrite 1.) 0 deg C, 1 h, 2.) reflux, 2 h; Yield given. Multistep reaction; |
2-Dimethylaminomethyl-3,5-dimethyl-phenol
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With 1,4-dioxane; copper oxide-chromium oxide at 165℃; Hydrogenolyse; |
Conditions | Yield |
---|---|
With hydrogen iodide; acetic acid at 150℃; |
4-Hexadecyloxy-2,3,6-trimethyl-phenol
acetic anhydride
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With hydrogen iodide; acetic acid at 150℃; |
Conditions | Yield |
---|---|
With sulfuric acid at 20℃; |
Conditions | Yield |
---|---|
With activated bauxit at 450℃; under 12503.6 Torr; |
methanol
3,5-Dimethylphenol
A
2,3,5-trimethylphenol
B
2,3,5,6-tetramethylphenol
C
pentamethylphenol
Conditions | Yield |
---|---|
at 450℃; under 7355.08 - 12503.6 Torr; Leiten ueber aktivierten Bauxit; |
2,3,5-trimethylphenol
bromoacetic acid methyl ester
(2,3,5-Trimethyl-phenoxy)-acetic acid methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In butanone for 5.5h; Heating; | 100% |
trifluoromethylsulfonic anhydride
2,3,5-trimethylphenol
2,3,5-Trimethylphenyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
In pyridine at 0 - 20℃; for 1h; | 100% |
With triethylamine In toluene at 20℃; Flow reactor; |
Conditions | Yield |
---|---|
With sodium hydride In dimethyl sulfoxide for 10h; Ambient temperature; | 99.8% |
With sodium hydride In dimethyl sulfoxide for 10h; | 98% |
Stage #1: 2,3,5-trimethylphenol With sodium hydride In tetrahydrofuran at 0℃; for 1h; Stage #2: methyl iodide In tetrahydrofuran at 0℃; for 3h; | 92% |
2,3,5-trimethylphenol
C18H23O2PS2
Conditions | Yield |
---|---|
With tetraphosphorus decasulfide for 0.0694444h; Microwave irradiation; | 99.3% |
2,3,5-trimethylphenol
carbonic acid dimethyl ester
2,3,5-trimethylanisole
Conditions | Yield |
---|---|
With dimanganese decacarbonyl at 180℃; for 1h; Reagent/catalyst; | 99% |
Conditions | Yield |
---|---|
Stage #1: 2,3,5-trimethylphenol With tetraphosphorus decasulfide In chloroform at 35℃; Stage #2: triethylamine In chloroform | 98% |
2,3,5-trimethylphenol
propionic acid
Conditions | Yield |
---|---|
With titanium tetrachloride In neat (no solvent) at 100℃; for 5h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With bis(η3-allyl-μ-chloropalladium(II)); caesium carbonate; XPhos In tetrahydrofuran; acetonitrile at 120℃; Inert atmosphere; regioselective reaction; | 98% |
2,3,5-trimethylphenol
3-Chloro-2-methylpropene
2,3,5-Trimethyl-1-(2-methyl-2-propenyloxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide; acetone Heating; | 97% |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 3h; | |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 3h; |
Conditions | Yield |
---|---|
With titanium superoxide; dihydrogen peroxide; acetic acid In water at 50℃; for 2h; | 96% |
With oxygen In water; acetonitrile at 40℃; under 15001.5 Torr; for 1h; Green chemistry; | 94% |
With 5,10,15,20-tetrakis(2,6-dichlorophenyl)porphyrin; oxygen In chloroform; acetonitrile for 24h; Product distribution; Further Variations:; Reagents; Irradiation; | 93% |
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 3h; | 96% |
2-methyl-3-bromo-1-propene
2,3,5-trimethylphenol
2,3,5-Trimethyl-1-(2-methyl-2-propenyloxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 15h; | 96% |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 15h; | 96% |
trimethylsilyl isothiocyanate
2,3,5-trimethylphenol
2,3,5-trimethyl-4-thiocyanatophenol
Conditions | Yield |
---|---|
With 1-chloro-1λ3-benzo[d][1,2]iodaoxol-3(1H)-one In dichloromethane at 20℃; for 1h; | 96% |
2,3,5-trimethylphenol
allyl bromide
1,2,5-trimethyl-3-(prop-2-en-1-yloxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 80℃; | 95% |
With potassium carbonate; acetone | |
With sodium hydroxide In N,N-dimethyl-formamide |
2,3,5-trimethylphenol
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide In methanol; dichloromethane for 0.333333h; | 95% |
With 1-butyl-3-methylimidazolium tribromide at -10℃; | 86% |
2,3,5-trimethylphenol
2-Bromoacetyl bromide
Bromo-acetic acid 2,3,5-trimethyl-phenyl ester
Conditions | Yield |
---|---|
With pyridine In diethyl ether for 1h; Ambient temperature; | 94% |
Conditions | Yield |
---|---|
With potassium hydroxide; Raney Ni-Al; water at 90℃; for 20h; | 91.2% |
With nickel at 155℃; Hydrogenation; | |
With nickel; sodium(2,3,5-(methyl)3phenoxide) at 170℃; under 95616 - 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With iodine; oxygen; copper(II) nitrate In water at 80℃; under 760.051 Torr; for 3h; Green chemistry; regioselective reaction; | 91% |
With hydrogenchloride; potassium iodate; potassium iodide In methanol at 20℃; for 0.5h; | 62.2% |
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl acetamide at 20℃; Heating; | 91% |
2,2-(dimethyl)-2-phenylacetaldehyde
2,3,5-trimethylphenol
2,2,4,6,7-pentamethyl-3-phenyl-2,3-dihydrobenzofuran
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In toluene at 110℃; for 1h; | 90% |
2-chloroethyl ethyl ether
2,3,5-trimethylphenol
1-(2-ethoxyethoxy)-2,3,5-trimethylbenzene
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 20 - 70℃; for 48h; | 90% |
2,3,5-trimethylphenol
4,4-dimethoxy-3,5-dimethylcyclohexa-2,5-dien-1-one
Conditions | Yield |
---|---|
With methanesulfonic acid at 20℃; regioselective reaction; | 90% |
Conditions | Yield |
---|---|
With C62H54Cl2N4Pd2; trifluoroacetic acid at 20℃; for 12.0833h; Cooling with ice; regioselective reaction; | 90% |
2,3,5-trimethylphenol
7-(4-fluorophenyl)-7-hydroxyheptanoic acid
7-(4-fluorophenyl)-7-(2-hydroxy-3,4,6-trimethylphenyl)heptanoic acid
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane at 60℃; for 6h; | 89% |
2,3,5-trimethylphenol
Ethyl 2-bromopropionate
ethyl 2-(2,3,5-trimethylphenyl)oxypropionate
Conditions | Yield |
---|---|
With potassium iodide In N,N-dimethyl-formamide; acetone Heating; | 89% |
2,3,5-trimethylphenol
1-(3-methoxyphenyl)-2-(2,3,5-trimethylphenoxy)ethanone
Conditions | Yield |
---|---|
88% |
Conditions | Yield |
---|---|
With tin(IV) chloride In neat (no solvent) at 100℃; for 8h; Inert atmosphere; chemoselective reaction; | 88% |
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