CAS No.32360-03-5,2-tert-Butyl-5-pentadecylphenol Suppliers

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5-pentadecyl-2-tert-butyl-phenol

Cas:32360-03-5

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

Zhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed

2-tert-Butyl-5-pentadecylphenol

Cas:32360-03-5

Min.Order:1 Kilogram

FOB Price: $2.0

Type:Lab/Research institutions

inquiry

Shandong Mopai Biotechnology Co., LTD

Shandong Mopai Biotechnology 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 chemicals. W

5-pentadecyl-2-tert-butyl-phenol

Cas:32360-03-5

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

factory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents

5-pentadecyl-2-tert-butyl-phenol

Cas:32360-03-5

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Zibo Hangyu Biotechnology Development Co., Ltd

home-produced Application:medicine

2-tert-Butyl-5-pentadecylphenol

Cas:32360-03-5

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Synthetic route

: 1634-04-4
tert-butyl methyl ether

: 501-24-6
3-n-Pentadecylphenol

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

Conditions

Conditions	Yield
tin(IV) chloride In dichloromethane for 16h; Ambient temperature;	98%

: 507-20-0
tertiary butyl chloride

: 501-24-6
3-n-Pentadecylphenol

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

Conditions

Conditions	Yield
With zinc(II) chloride In acetone at 60℃; for 3h; Temperature;
With zinc(II) chloride In acetone at 50℃; for 5h;	31.2 g

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 106-93-4
ethylene dibromide

: 2-(2-bromo-ethoxy)-1-tert-butyl-4-pentadecyl-benzene

Conditions

Conditions	Yield
With potassium hydroxide at 70℃; for 6h;	88%

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 106-95-6
allyl bromide

: 502495-06-9
2-allyloxy-1-tert-butyl-4-n-pentadecylbenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone Heating;	80%

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 4392-24-9
Cinnamyl bromide

: 1-tert-butyl-4-n-pentadecyl-2-(3-phenylallyloxy)benzene

Conditions

Conditions	Yield
With potassium carbonate In acetone Heating;	79%

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 3-n-pentadecyl-6-tert-butyl-2,4-dinitrophenol

Conditions

Conditions	Yield
With nitric acid In methanol at 20℃; for 0.5h;	79%

: 4784-77-4, 39616-19-8, 29576-14-5
(E)-1-Bromo-2-butene

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2-(but-2-enyloxy)-1-tert-butyl-4-n-pentadecylbenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone Heating;	77%

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 265310-65-4
2-tert-butyl-5-n-pentadecyl-1,4-benzoquinone

Conditions

Conditions	Yield
With water; dihydrogen peroxide; acetic acid; methyltrioxorhenium(VII) at 25℃; for 12h; Catalytic oxidation;	71%
With poly(4-vinylpyridine) 25 percent cross-linked; dihydrogen peroxide; methyltrioxorhenium(VII) In ethanol; water at 40℃;
Multi-step reaction with 2 steps 1: K2CO3 / dimethylformamide / 12 h / 25 °C 2: 49 percent / H2O2; H2O; AcOH / methyltrioxorhenium(VII) / 12 h / 25 °C View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

A: 3-n-pentadecyl-6-tert-butyl-2-nitrophenol

B: 2-tert-butyl-5-n-pentadecyl-4-nitrophenol

Conditions

Conditions	Yield
With nitric acid In methanol at 20℃; for 0.5h;	A 15% B 69%

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 172759-21-6
2-tert-butyl-4-bromo-5-n-pentadecylphenol

Conditions

Conditions	Yield
With bromine In tetrachloromethane at 0℃; for 0.25h;

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 74-88-4
methyl iodide

: 265310-67-6
2-tert-Butyl-5-n-pentadecylphenyl methyl ether

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 12h; Methylation;

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 5-tert-butyl-3-nitro-2-pentadecyl-[1,4]benzoquinone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 15 percent / HNO3 / methanol / 0.5 h / 20 °C 2: 25 percent / methylrhenium trioxide; aq. H2O2; AcOH / 4 h / 80 °C View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 5-tert-butyl-3-nitro-2-pentadecyl-benzene-1,4-diol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 15 percent / HNO3 / methanol / 0.5 h / 20 °C 2: 26 percent / methylrhenium trioxide; aq. H2O2; AcOH / 4 h / 80 °C View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 699008-88-3
4-[2-(2-tert-butyl-5-pentadecyl-phenoxy)-ethoxy]-benzaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 88 percent / KOH / 6 h / 70 °C 2: 60 percent / K2CO3 / acetone / 24 h / Heating View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2-allyl-6-tert-butyl-3-n-pentadecylphenol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 80 percent / K2CO3 / acetone / Heating View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 6-tert-butyl-2-(1-methylallyl)-3-n-pentadecylphenol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 77 percent / K2CO3 / acetone / Heating View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 9-tert-butyl-6-n-pentadecyl-4,5-dihydro-3H-benzo[b]oxepin-2-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 80 percent / K2CO3 / acetone / Heating 2: 90 percent / 1,4-bis(diphenylphosphino)butane; H2 / Pd(OAc)2 / toluene / 24 h / 100 °C / 31028.9 Torr View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2-tert-butyl-5-n-pentadecyl-4-(3-phenylallyl)phenol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 79 percent / K2CO3 / acetone / Heating View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 265310-66-5
2-tert-Butyl-5-n-pentadecyl-p-hydroquinone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 71 percent / H2O2; H2O; AcOH / methyltrioxorhenium(VII) / 12 h / 25 °C 2: 100 percent / NaBH4 / ethanol; tetrahydrofuran / 1 h / 25 °C View Scheme
Multi-step reaction with 3 steps 1: K2CO3 / dimethylformamide / 12 h / 25 °C 2: 49 percent / H2O2; H2O; AcOH / methyltrioxorhenium(VII) / 12 h / 25 °C 3: 100 percent / NaBH4 / ethanol; tetrahydrofuran / 1 h / 25 °C View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2,4-dibromo-6-tert-butyl-3-n-pentadecylphenol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: Br2 / CCl4 / 0.25 h / 0 °C 2: Br2 / CCl4 / Heating View Scheme

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2,4,4-tribromo-6-tert-butyl-3-n-pentadecylphenol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Br2 / CCl4 / 0.25 h / 0 °C 2: Br2 / CCl4 / Heating 3: Br2, acetic acid / Ambient temperature View Scheme

: 50-00-0
formaldehyd

: 32360-03-5
2-tert-butyl-5-n-pentadecylphenol

: 2,2’-methylenebis(3-pentadecyl-6-tert-butylphenol)

Conditions

Conditions	Yield
With sodium hydroxide In ethanol; water for 3h; Time; Reflux;
With sodium hydroxide In ethanol; water for 5h; Reflux;

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Antimex Chemical Limied

Zibo Hangyu Biotechnology Development Co., Ltd

Synthetic route

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