CAS No.496-78-6,2,4,5-Trimethylphenol Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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Henan Tianfu Chemical Co., Ltd.

Product Name: 2,4,5-TRIMETHYLPHENOL Synonyms: 1-Hydroxy-2,4,5-trimethylbenzene;2,4,5-trimethyl-pheno;5-hydroxypseudocumene;PSEUDOCUMENOL;2,4,5-TRIMETHYLPHENOL;Phenol, 2,4,5-trimethyl- CAS: 496-78-6 MF: C9H12O MW: 136.19 Appearance:white pow

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

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Shandong Mopai Biotechnology Co., LTD

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Win-Win chemical Co.Ltd

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Antimex Chemical Limied

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Hangzhou Fandachem Co.,Ltd

Phenol,2,4,5-trimethyl- cas 496-78-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

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Henan Kanbei Chemical Co.,LTD

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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HeBei Oriental Industry Co., Ltd

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Hangzhou Share Chemical Co., Ltd

At Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi

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Shanghai united Scientific Co.,Ltd.

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Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 2,4,5-TRIMETHYLPHENOL, CAS:496-78-6 with the most competitive price and the best qual

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Skyrun Industrial Co.,Ltd

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2,4,5-TriMethylphenol, 99%

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Chemical Co.Ltd

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Synthetic route

: 10496-92-1
4,5-dimethyl-2-hydroxybenzyl alcohol

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With 1% Pd/C; hydrogen In methanol	100%

: 89711-25-1
2,4,5-Trimethyl-3-methylsulfanyl-phenol

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With nickel In methanol for 2h; Heating;	99%

: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With water; hydrogen bromide; Aliquat 336 at 105℃; for 8h; Catalytic behavior;	75%

: 4906-82-5
6-acetoxy-2,4,6-trimethyl-cyclohexa-2,4-dienone

A: 496-78-6
2,4,5-trimethylphenol

B: 55977-89-4
Essigsaeure-(3-hydroxy-2,4,6-trimethylphenyl)ester

: (RS)-6-exo-Acetoxy-3,5,6-trimethylbicyclo<3.1.0>hex-3-en-2-on

D: (RS)-4-Acetoxy-2,4,5-trimethylcyclohexa-2,5-dien-1-on

Conditions

Conditions	Yield
With 2,2,2-trifluoroethanol for 2h; Ambient temperature; Irradiation; Further byproducts given;	A 2.2% B 1.6% C 45% D 27%

...Expand

: 67-56-1
methanol

: 95-65-8
3,4-Dimethylphenol

A: 527-54-8
3,4,5-trimethylphenol

B: 496-78-6
2,4,5-trimethylphenol

C: 526-85-2
2,3,4-trimethylphenol

Conditions

Conditions	Yield
Pd-containing mordenite at 350℃;	A 1% B 40% C 45%

...Expand

: 38441-63-3
2,4,4-Trimethyl-2,5-cyclohexadien-1-on

: 3908-55-2
Trimethyl(methylthio)silane

A: 496-78-6
2,4,5-trimethylphenol

B: 1215002-19-9
C10H14S

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid In dichloromethane for 168h; Reflux;	A 39% B 42%

...Expand

: 38441-63-3
2,4,4-Trimethyl-2,5-cyclohexadien-1-on

: 4551-15-9
phenylthiotrimethylsilane

A: 496-78-6
2,4,5-trimethylphenol

B: 1215002-21-3
phenyl(2,4,5-trimethylphenyl)sulfane

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid In dichloromethane for 168h; Reflux;	A 35% B 32%

...Expand

: 95-63-6
1,2,4-Trimethylbenzene

A: 16308-92-2
2,4-dimethylbenzyl alcohol

B: 700-13-0
Trimethylhydroquinone

C: 496-78-6
2,4,5-trimethylphenol

D: 53957-33-8
2,5-dimethylbenzyl alcohol

Conditions

Conditions	Yield
With glucose dehydrogenase; D-glucose; P450 BM3 R47S, Y51W mutant; NADPH; catalase; ascorbic acid In aq. phosphate buffer; dimethyl sulfoxide pH=7.5; Catalytic behavior; Enzymatic reaction;	A 31% B 12% C 34% D 12%

...Expand

: 95-63-6
1,2,4-Trimethylbenzene

A: 16308-92-2
2,4-dimethylbenzyl alcohol

B: 6966-10-5
3,4-dimethylbenzyl alcohol

C: 496-78-6
2,4,5-trimethylphenol

D: 2416-94-6
2,3,6-trimethylphenol

E: 697-82-5
2,3,5-trimethylphenol

F: 53957-33-8
2,5-dimethylbenzyl alcohol

Conditions

Conditions	Yield
With glucose dehydrogenase; D-glucose; P450 BM3; NADPH; catalase; ascorbic acid In aq. phosphate buffer; dimethyl sulfoxide pH=7.5; Catalytic behavior; Enzymatic reaction;	A 27% B 5% C 34% D 9% E 8% F 14%

...Expand

: 95-63-6
1,2,4-Trimethylbenzene

A: 16308-92-2
2,4-dimethylbenzyl alcohol

B: 700-13-0
Trimethylhydroquinone

C: 496-78-6
2,4,5-trimethylphenol

D: 697-82-5
2,3,5-trimethylphenol

E: 53957-33-8
2,5-dimethylbenzyl alcohol

Conditions

Conditions	Yield
With glucose dehydrogenase; D-glucose; P450 BM3 R47S, Y51W, I401M mutant; NADPH; catalase; ascorbic acid In aq. phosphate buffer; dimethyl sulfoxide pH=7.5; Catalytic behavior; Reagent/catalyst; Enzymatic reaction;	A 17% B 32% C 31% D 7% E 7%

...Expand

: 95-63-6
1,2,4-Trimethylbenzene

A: 16308-92-2
2,4-dimethylbenzyl alcohol

B: 700-13-0
Trimethylhydroquinone

C: 496-78-6
2,4,5-trimethylphenol

D: 2416-94-6
2,3,6-trimethylphenol

E: 697-82-5
2,3,5-trimethylphenol

F: 53957-33-8
2,5-dimethylbenzyl alcohol

Conditions

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%

...Expand

: 95-65-8
3,4-Dimethylphenol

: 75-11-6
diiodomethane

A: 496-78-6
2,4,5-trimethylphenol

B: 526-85-2
2,3,4-trimethylphenol

Conditions

Conditions	Yield
With diethylzinc In toluene for 1.58333h; Inert atmosphere; Reflux;	A 3% B 2%

...Expand

: 917-64-6
methyl magnesium iodide

: 137-18-8
2,5-Dimethyl-1,4-benzoquinone

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield

: 68097-96-1
1-<(4-Hydroxy-3,6-dimethyl-phenyl)-methyl>-piperidin

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With 1,4-dioxane; copper oxide-chromium oxide at 165℃; under 73550.8 Torr; Hydrogenolyse;

: 85231-15-8
4-formyl-2,5-dimethylphenol

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With hydrogenchloride; amalgamated zinc; toluene

: 137-17-7
2,4,5-trimethylaniline

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
Diazotization;
(i) NaNO2, H2SO4, (ii) H2O; Multistep reaction;

: 3453-84-7
2,4,5-trimethylbenzenesulfonic acid

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With potassium hydroxide beim Verschmelzen;

: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

: 628-13-7
pyridine hydrochloride

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield

: nitroso-(2,4,5-trimethyl-phenyl)-amidosulfuric acid

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With water

: 90765-52-9
1,2,5-Trimethyl-cyclohexen-(2)-ol-(3)-on-(4)

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With phosphoric acid

: 7474-10-4
3,4,6-trimethyl-2-cyclohexen-1-one

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
palladium on barium sulfate In biphenyl

: 633337-82-3
7-methoxy-4,6-dimethyl-3H-isobenzofuran-1-one

: 10034-85-2
hydrogen iodide

red phosphorus: red phosphorus

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield

...Expand

trimer(ic) 4.5.7-trimethyl-coumarone: trimer(ic) 4.5.7-trimethyl-coumarone

A: 1027417-43-1
4,5,7-trimethyl-benzofuran

B: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield

: 7758-99-8
copper(II) sulfate

: 64-19-7
acetic acid

: 90565-17-6
(2,4,5-trimethyl-phenyl)-hydrazine

A: 95-63-6
1,2,4-Trimethylbenzene

B: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield

...Expand

sodium salt of/the/ N-<2.4.5-trimethyl-phenyl>-hydrazine-N'-sulfonic acid: sodium salt of/the/ N-<2.4.5-trimethyl-phenyl>-hydrazine-N'-sulfonic acid

A: 496-78-6
2,4,5-trimethylphenol

B: 90565-17-6
(2,4,5-trimethyl-phenyl)-hydrazine

Conditions

Conditions	Yield
With hydrogenchloride

: 75-09-2
dichloromethane

: 95-63-6
1,2,4-Trimethylbenzene

: 359-48-8
trifluoroacetyl peroxide

A: 935-92-2
2,3,5-Trimethyl-1,4-benzoquinone

B: 496-78-6
2,4,5-trimethylphenol

C: 2416-94-6
2,3,6-trimethylphenol

D 4-hydroxy-2,4,5-trimethyl-cyclohexa-2,5-dienone (?): 4-hydroxy-2,4,5-trimethyl-cyclohexa-2,5-dienone (?)

Conditions

Conditions	Yield

...Expand

: 95-63-6
1,2,4-Trimethylbenzene

A: 527-60-6
Mesitol

B: 496-78-6
2,4,5-trimethylphenol

C: 2416-94-6
2,3,6-trimethylphenol

D: 697-82-5
2,3,5-trimethylphenol

E ArCH2OH, ArCH2Ar',: ArCH2OH, ArCH2Ar',

Conditions

Conditions	Yield
palladium diacetate; sodium persulfate In acetic acid at 115℃; for 3h; Product distribution; other oxidants: NaNO3, HPA-2, H2O2, AgNO3; other other reaction times and temperatures;

...Expand

acidic 1.2.4-trimethyl-benzenediazonium sulfate-(5): acidic 1.2.4-trimethyl-benzenediazonium sulfate-(5)

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
With sulfuric acid Sonnenlicht;

: 3453-84-7
2,4,5-trimethylbenzenesulfonic acid

potash: potash

: 496-78-6
2,4,5-trimethylphenol

Conditions

Conditions	Yield
beim Schmelzen;

: 496-78-6
2,4,5-trimethylphenol

: 96-32-2
bromoacetic acid methyl ester

: 95450-50-3
(2,4,5-Trimethyl-phenoxy)-acetic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In butanone for 5.5h; Heating;	100%

: 79-21-0
peracetic acid

: 496-78-6
2,4,5-trimethylphenol

A: 13038-87-4
2,3,5-trimethyl-1,6-benzoquinone

B: 69305-42-6
1-acetoxy-2,4,5-trimethylbenzene

C: 4537-09-1
1,4-dimethoxy-2,3,5-trimethyl-benzene

D: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

: 5-acetoxy-2,4-dihydroxy-2,4,5-trimethyl-3,6-lacto-1-hexanoic acid

Conditions

Conditions	Yield
sulfuric acid at 50℃; for 0.5h; Mechanism; Thermodynamic data; effect of catalysts;	A n/a B 0.03% C 0.07% D 0.07% E 99.76%

...Expand

: 496-78-6
2,4,5-trimethylphenol

: 5-acetoxy-2,4-dihydroxy-2,4,5-trimethyl-3,6-lacto-1-hexanoic acid

Conditions

Conditions	Yield
With peracetic acid; sulfuric acid at 50℃; for 0.5h;	99.76%

: 496-78-6
2,4,5-trimethylphenol

: 64-19-7
acetic acid

A: 13038-87-4
2,3,5-trimethyl-1,6-benzoquinone

B: 69305-42-6
1-acetoxy-2,4,5-trimethylbenzene

C: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

D: 36592-62-8
4-acetoxy-2,3,5-trimethylphenol

E: 109576-73-0
3-acetoxy-2,5-dihydroxy-5-carboxy-2,3,5-trimethylpentan-4-olide

Conditions

Conditions	Yield
With peracetic acid at 50℃; for 0.25h; Product distribution; Kinetics; Thermodynamic data;	A 0.03% B 0.03% C 0.06% D 0.06% E 97.8%

...Expand

: 496-78-6
2,4,5-trimethylphenol

: Diphenyliodonium fluoride

: C15H16O

Conditions

Conditions	Yield
With sodium hydrogencarbonate In dichloromethane at 40℃;	90%

: 358-23-6
trifluoromethylsulfonic anhydride

: 496-78-6
2,4,5-trimethylphenol

: 2,3,5-trimethylphenyl trifluoromethanesulfonate

Conditions

Conditions	Yield
In pyridine; dichloromethane at 0 - 20℃; for 2h; Inert atmosphere;	90%

: 496-78-6
2,4,5-trimethylphenol

: 103187-28-6
7-(4-fluorophenyl)-7-hydroxyheptanoic acid

: 121099-56-7
7-(4-fluorophenyl)-7-(2-hydroxy-3,5,6-trimethylphenyl)heptanoic acid

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane at 60℃; for 6h;	78%

: 496-78-6
2,4,5-trimethylphenol

: sodium[tertrakis(2,4,5-trimethylphenoxy)borate]

Conditions

Conditions	Yield
Stage #1: With boric acid In toluene for 12h; Heating; Stage #2: 2,4,5-trimethylphenol With sodium In tetrahydrofuran at 20℃;	71%

: 1040913-82-3
sodium 2,4,5-trimethylphenolate

: 496-78-6
2,4,5-trimethylphenol

: 11113-50-1
boric acid

: sodium[tertrakis(2,4,5-trimethylphenoxy)borate]

Conditions

Conditions	Yield
In toluene phenol (excess) and acid heated for 2 h (Dean-Stark trape), volatiles removed (vac.), dissolved (THF), added dropwise to a soln. of Na compd. (THF), stirred for 1-12 h; ppt. filtered, washed (diethyl ether, pentane), dried (high vac.); elem.anal.;	71%

...Expand

: 496-78-6
2,4,5-trimethylphenol

: 4-(2-oxoimidazolidin-1-yl)benzene-1-sulfonyl chloride

: 1311945-68-2
2,4,5-trimethylphenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 25℃; for 24h; Inert atmosphere;	69%

: 496-78-6
2,4,5-trimethylphenol

: 37831-62-2
ethyl 4-chloronicotinate

: 1415407-43-0
ethyl 4-(2,4,5-trimethylphenoxy)nicotinate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 3h;	69%

: 50-00-0
formaldehyd

: 496-78-6
2,4,5-trimethylphenol

: 2-hydroxymethyl-3,4,6-trimethylphenol

Conditions

Conditions	Yield
With sodium hydroxide	59%
With extinguished lime; water; calcium carbonate at 50℃;

: 496-78-6
2,4,5-trimethylphenol

: 110932-47-3
3,3',4,4',5,5'-hexamethyl-2,2'-biphenol

Conditions

Conditions	Yield
With 4,4'-di-tert-butylbiphenyl; 10-methyl-9-(2,4,6-trimethylphenyl) acridinium tetrafluoroborate In 1,2-dichloro-ethane at 35℃; Solvent; Irradiation;	56%
With selenium(IV) oxide; acetic acid at 85℃;	39%
With trifluoroacetic acid at 30℃; Ionic liquid; Electrochemical reaction;	30%
With tetraethylammonium methyl sulfate In hexafluoropropan-2-ol at 50℃; Electrolysis;	22%

: 67-56-1
methanol

: 496-78-6
2,4,5-trimethylphenol

: 5-methoxy-2,3-dimethylbenzyl methyl ether

Conditions

Conditions	Yield
With chlorine In dichloromethane -60 deg C -> room temperature;	53%

: 496-78-6
2,4,5-trimethylphenol

: C18H22O2Se

Conditions

Conditions	Yield
With pyridine; selenium(IV) oxide at 55℃;	40%

: 496-78-6
2,4,5-trimethylphenol

: 74-88-4
methyl iodide

: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

Conditions

Conditions	Yield
Stage #1: 2,4,5-trimethylphenol With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; Solvent;	32%

: 2832-19-1
2-Chloro-N-(hydroxymethyl)acetamide

: 496-78-6
2,4,5-trimethylphenol

: 51571-06-3
2-Aminomethyl-3,4,6-trimethyl-phenol; hydrochloride

Conditions

Conditions	Yield
With hydrogenchloride In ethanol for 0.5h; Heating;	22%

: 496-78-6
2,4,5-trimethylphenol

: 57-15-8
1,1,1-trichloro-2-methyl-2-propanol

: 86550-00-7
2-(2,4,5-Trimethylphenoxy)isobutyric Acid

Conditions

Conditions	Yield
With sodium hydroxide In acetone for 21h; temp. below 35 degC;	20%

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