As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis
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inquiryWhy is SINOWAY: 1) Specialized in pharmaceutical and healthcare industrial for 34 years. 2) ISO 9001:2015 & SGS audited supplier . 3) Accept various payment terms : T.T 30-60 days. 4) We have warehouse in USA with quickly shipment . 5) We c
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inquiryItems Standard Result Appearance Yellow to orange crystalline powder Complies Identificatio A: I
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inquiryCoenzyme Q10/Ubidecarenone[CAS:303-98-0] With about ten years of business experiences on the marketing & distribution, thinkchem specializes in exporting pharmaceuticals, veterinary drugs, feed additives, intermediates, fine chemicals, plan
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inquirycoenzyme Q10 Quick Details CAS No.: 20140909 Other Names: Vitamin MF: CxHyOzNn Place of Origin: Shaanxi, China (Mainland) Type: Vi
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inquiryCoenzyme Q10 Product:COENZYME Q10 CAS No 303-98-0 Application Pharmaceuticals cosmetics food additive and so on. Molecular formula:C59H90O4 Molucular weight:863.34 Synonyms:Ubiquinone-10, CoQ10, Ubiquinone 50, Ubidecarenone
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inquiryCoenzyme Q10 Powder Specification:10%,20%,40% CoQ10 (Water-soluble);98%-101% CoQ10 (Oil/fat-soluble) INCI: Ubiquinone Appearance:Yellow or light yellow crystalline power Certificate:ISO9001//Kosher/Organic/halal/COSMOS International certification s
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryHangzhou Huarong Pharm Co., Ltd. established since 2009 , has been always focusing on supplying products and services to our clients in the field of small molecule drug. Huarong Pharm has built platforms for the research, development and manufac
UbidecarenoneCAS:303-98-0 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 intermediates,
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inquiryProName:Factory supply Coenzyme Q10 powder CAS... CasNo:303-98-0 Molecular Formula:C59H90O4 Appearance:Yellow to organge crystalline powder Application:nutrition and supplements; Cosmetic DeliveryTime:within 7 days after your final confirm...
Zhonghe Fountain is striving for R&D,production and distribution cosmetic active ingredients for personal care industry. Zhonghe Fountain always maintains a keen insight into industry and focuses on the market demand trends to expand its invests
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inquiryWe are very strong on this product. Application:nutrition
Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquirySuperiority pioneerbiotech is a leading manufacturer and supplier of chemicals in China. We develop ,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals. We could give you: 1.Best q
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inquiryJinlan Pharm-Drugs Technology Co.,Limited (with its export company Hangzhou Royall Import & Export Co.,Ltd.)is located in Hangzhou, Zhejiang Province. Neighboring Ningbo port, Shanghai port, Hangzhou Xiaoshan Int’l Airport and Shanghai Pu
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; ...... Appearance:Yellow to orange crystalline powder Storage:-20°C Package:1kg
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inquirySleeping pills and stability.This product is white or white crystalline powder;Odourless and slightly bitter taste.Almost insoluble in water, soluble in hydrochloric acid.In acid or alkali and heat hydrolysis, oral drug under the action of gastric
Xi’an Quanao Biotech Co., Ltd. with 18 years experience in plant extract filed. Product grade: Medicine, Health care product, Cosmetics, Food, Beverage, Feed. Hot selling market: Europe, North America, South America, Middle East, Asia Pacifi
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inquiry1, Full experience of large numbers containers loading in main Chinese seaports 2, Packing with pallet as buyer's special request 3, Best service after shipment with e-mail 4, Cargoes together with container sales service available
Product description: Product name Ubidecarenone CAS number 303-98-0 Assay ≥99% Appearance Yellow or orange-yellow crystalline powder Capacity 200mt/year Application Widely us
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inquiryhigh quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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Shanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
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inquiryColorcom is a global leader in industrial chemical manufacturing and is continuously innovating and transforming to exceed client expectations and industry standards. Colorcom prides itself on superior customer and technical focus, while focusing on
ubidecarenone
Conditions | Yield |
---|---|
In toluene for 0.5h; Heating; | 100% |
2-hydroxy-3,4,5-trimethoxy-6-((2E)-decaprenyl)-toluene
ubidecarenone
Conditions | Yield |
---|---|
With iron(III) chloride In dichloromethane; acetonitrile at 0 - 5℃; for 0.5h; Product distribution / selectivity; | 100% |
With iron(III) chloride In dichloromethane; water; acetonitrile at 0 - 5℃; for 0.5h; Product distribution / selectivity; | 100% |
With iron(III) chloride In di-isopropyl ether; water; ethyl acetate at 0 - 5℃; for 0.5h; Product distribution / selectivity; | 95% |
ubidecarenone
Conditions | Yield |
---|---|
In ethanol; hexane at 25℃; for 0.733333h; Purification / work up; | 99.8% |
1-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzene
ubidecarenone
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride In ethanol; hexane; water at 20℃; for 3h; | 95% |
With hydrogenchloride; air In methanol; hexane at 40℃; for 4h; | 93% |
With hydrogenchloride In methanol; hexane at 40℃; for 4h; | 93% |
With air; hydrogen cation Yield given. Multistep reaction; |
2-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-phenol
ubidecarenone
Conditions | Yield |
---|---|
With salcomine; oxygen In N,N-dimethyl-formamide; toluene at 20℃; for 24h; | 94% |
With pyridine; oxygen; sodium carbonate; salcomine In toluene; acetonitrile for 16h; Product distribution / selectivity; | 69% |
ubiquinol
ubidecarenone
Conditions | Yield |
---|---|
With sodium hydrogencarbonate at 50℃; pH=8; Temperature; pH-value; | 90.6% |
With oxygen In ethanol for 24h; Conversion of starting material; | 46% |
With oxygen; acetic acid In ethanol for 24h; Conversion of starting material; | 41% |
trimethylaluminum
2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone
(all-E)-2,6,10,14,18,22,26,30,34-nonamethyl-2,6,10,14,18,22,26,30,34-nonacontanonaen-38-yne
ubidecarenone
Conditions | Yield |
---|---|
Stage #1: trimethylaluminum; (all-E)-2,6,10,14,18,22,26,30,34-nonamethyl-2,6,10,14,18,22,26,30,34-nonacontanonaen-38-yne With zirconocene dichloride In 1,2-dichloro-ethane at 23℃; for 1h; Stage #2: 2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone With n-butyllithium; Cl2Ni(PPh)2; triphenylphosphine In tetrahydrofuran at 23℃; for 1h; Further stages.; | 90% |
Stage #1: trimethylaluminum; (all-E)-2,6,10,14,18,22,26,30,34-nonamethyl-2,6,10,14,18,22,26,30,34-nonacontanonaen-38-yne; zirconocene dichloride In dichloromethane; chlorobenzene at -15 - 0℃; Stage #2: 2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone With bis(triphenylphosphine)nickel(II) chloride; n-butyllithium In tetrahydrofuran at -20℃; for 2h; Further stages.; | 89% |
Stage #1: trimethylaluminum; (all-E)-2,6,10,14,18,22,26,30,34-nonamethyl-2,6,10,14,18,22,26,30,34-nonacontanonaen-38-yne With methylalumoxane; rac-ethylenebis(1-indenyl)zirconium(IV) chloride In toluene at 20℃; for 22h; Negishi carboalumination; Stage #2: 2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone; bis(triphenylphosphine)nickel(II) chloride; n-butyllithium In tetrahydrofuran at -20℃; for 2h; | 88% |
ubidecarenone
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; nitric acid In tetrahydrofuran; water; acetonitrile at 0℃; for 0.5h; | 79% |
1,4-bis(benzyloxy)-2-{(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-5-[(4-methylphenyl)sulfonyl]tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl}-5,6-dimethoxy-3-methylbenzene
ubidecarenone
Conditions | Yield |
---|---|
With naphthalen-1-yl-lithium In tetrahydrofuran at -78℃; for 2h; | 77% |
(2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'E)-1-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2',6',10',14',18',22',26',30',34',38'-decaenyl)-6-methyl-2,3,4,5-tetramethoxybenzene
ubidecarenone
Conditions | Yield |
---|---|
With ceric ammoniumnitrate In dichloromethane; water; acetonitrile | 72% |
With ammonium cerium(IV) nitrate In dichloromethane; acetonitrile at 0℃; for 0.5h; | 61% |
With cerium(IV)diammonium nitrate; water In dichloromethane; acetonitrile at -5 - 3℃; for 1.28333h; |
ubidecarenone
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; nitric acid In tetrahydrofuran; water; acetonitrile at 0℃; for 0.5h; | 72% |
Conditions | Yield |
---|---|
Stage #1: 3,7,11,15,19,23,27,31,35,39,43-Undecamethyl-1,6,10,14,18,22,26,30,34,38,42-tetratetracontaundecaene-3-ol; 2,3-dimethoxy-5-methylbenzene-1,4-diol With scandium tris(trifluoromethanesulfonate) In nitromethane; hexane at 53℃; for 12h; Stage #2: With acetic acid; silver(l) oxide In hexane at 20℃; for 1h; Product distribution / selectivity; | 47.4% |
Stage #1: 3,7,11,15,19,23,27,31,35,39,43-Undecamethyl-1,6,10,14,18,22,26,30,34,38,42-tetratetracontaundecaene-3-ol; 2,3-dimethoxy-5-methylbenzene-1,4-diol With indium(III) chloride In nitromethane; hexane at 45 - 57℃; for 12h; Stage #2: With acetic acid; silver(l) oxide In hexane at 20℃; for 1h; Product distribution / selectivity; | 46.6% |
Stage #1: 3,7,11,15,19,23,27,31,35,39,43-Undecamethyl-1,6,10,14,18,22,26,30,34,38,42-tetratetracontaundecaene-3-ol; 2,3-dimethoxy-5-methylbenzene-1,4-diol With phosphotungstic acid In nitromethane; hexane at 52 - 53℃; for 12h; Stage #2: With acetic acid; silver(l) oxide In hexane at 20℃; for 1h; Product distribution / selectivity; | 45.2% |
2,3-dimethoxy-5-methylbenzene-1,4-diol
3,7,11,15,19,23,27,31,35,39-decamethyl-1,6,10,14,18,22,26,30,34,38-tetracontadecaene-3-ol
A
ubidecarenone
B
2-((2Z,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate 1) hexane, nitromethane, 10 min, 43 deg C, 2) 2-propanol, RT, 1 h; Yield given. Multistep reaction. Yields of byproduct given; |
ubiquinol
A
ubidecarenone
Conditions | Yield |
---|---|
With air In isopropyl alcohol at 25℃; for 3h; Yield given. Yields of byproduct given; |
(1,5-Dimethyl-4-hexenylidene)-triphenylphosphorane
2,3-dimethoxy-5-methyl-6-(33-formyl-3,7,11,15,19,23,27,31,35-octamethylhexatriacont-2E,6E,10E,14E,18E,22E,26E,30E-octaenyl)-1,4-benzoquinone
A
ubidecarenone
B
34'Z-ubiquinone-10
Conditions | Yield |
---|---|
In tetrahydrofuran at -20℃; for 0.5h; Title compound not separated from byproducts; |
2-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-benzene-1,4-diol
A
ubidecarenone
B
2-((2Z,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone
Conditions | Yield |
---|---|
With manganese(IV) oxide In diethyl ether at 0℃; Yield given. Yields of byproduct given; |
1-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-3,4-dimethoxy-2,5-bis-methoxymethoxy-6-methyl-benzene
A
ubidecarenone
B
co-enzyme Q10
Conditions | Yield |
---|---|
With silver(l) oxide; hydrogenchloride 1.) MeOH, CHCl3, stirring overnight: 2.) hexane, R.T. 30 min; Yield given. Multistep reaction. Yields of byproduct given; |
1-(5'-p-tosyl-all-trans-decaprenyl)-2-methyl-3,4,5,6-tetramethoxybenzene
A
ubidecarenone
B
2-((2E,5E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,5,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate; ethanol; sodium 1.) THF, 2 h, -20 to 0 deg C; 2.) CH2Cl2, CH3CN, H2O, 5 min, 0 deg C; Yield given. Multistep reaction. Yields of byproduct given; |
1,4-bis(benzyloxy)-2-{(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-5-[(4-methylphenyl)sulfonyl]tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl}-5,6-dimethoxy-3-methylbenzene
A
ubidecarenone
B
2-((2E,5E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,5,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone
Conditions | Yield |
---|---|
With oxygen; lithium; ethylamine 1.) THF, -70 deg C, 30 min; 2.) THF, MeOH, H2O, Et2O, 15 min; Yield given. Multistep reaction. Yields of byproduct given; |
1,4-dibenzyloxy-2,3-dimethoxy-5-methyl-6-(37'-phenylthio-3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'-decaenyl)benzene
A
ubidecarenone
B
2,3-dimethoxy-5-methyl-6-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,37'E-decaenyl)-1,4-benzoquinone
Conditions | Yield |
---|---|
With air; ammonia; iron(III) chloride; lithium 1.) ether, -70 deg C, 15 min, 2.) AcOH; Yield given. Multistep reaction. Yields of byproduct given; |
1,4-dibenzyloxy-2,3-dimethoxy-5-methyl-6-<37'-(4'',5''-dihydrothiazol-2''-yl)thio-3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'-decaenyl>benzene
A
ubidecarenone
B
2,3-dimethoxy-5-methyl-6-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,37'E-decaenyl)-1,4-benzoquinone
Conditions | Yield |
---|---|
With air; ammonia; iron(III) chloride; lithium 1.) Et2O, -40 deg C, 3 h, 2.) AcOH, 25 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
1,4-dibenzyloxy-2,3-dimethoxy-5-methyl-6-(37'-phenylsulfonyl-3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'-decaenyl)benzene
A
ubidecarenone
B
2,3-dimethoxy-5-methyl-6-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,37'E-decaenyl)-1,4-benzoquinone
Conditions | Yield |
---|---|
With air; iron(III) chloride; lithium; ethylamine 1.) -70 deg C, 15 min, THF, 2.) AcOH, 25 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; | |
With air; iron(III) chloride; lithium; ethylamine 1.) THF, -70 deg C, 15 min, 2.) AcOH, 25 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
1,4-dibenzyloxy-2,3-dimethoxy-5-methyl-6-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E/Z,38'-decaenyl)benzene
A
ubidecarenone
B
34'Z-ubiquinone-10
Conditions | Yield |
---|---|
With air; lithium; ethylamine 1.) THF, 2.) 25 deg C, 40 min; Multistep reaction. Title compound not separated from byproducts; |
1-Benzyloxy-3-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-4,5,6-trimethoxy-2-methyl-benzene
ubidecarenone
Conditions | Yield |
---|---|
With 1.); iron(III) chloride; lithium; ethylamine 1.) -78 deg C, 2.) ethyl acetate-isopropyl ether; Multistep reaction; |
2,3-Dimethoxy-5-methyl-1,4-benzoquinone
(all-E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl bromide
ubidecarenone
Conditions | Yield |
---|---|
Stage #1: (all-E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl bromide With tri-n-butyl-tin hydride; lithium diisopropyl amide In tetrahydrofuran; hexane for 2h; Stage #2: 2,3-Dimethoxy-5-methyl-1,4-benzoquinone With silver(l) oxide; boron trifluoride diethyl etherate In dichloromethane for 2h; Further stages.; |
1-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-2,3,4-trimethoxy-5-((2-methoxyethoxy)methoxy)-6-methylbenzene
ubidecarenone
Conditions | Yield |
---|---|
Stage #1: 1-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-2,3,4-trimethoxy-5-((2-methoxyethoxy)methoxy)-6-methylbenzene With water; hydrogen bromide In isopropyl alcohol at 50℃; for 4h; Stage #2: With iron(III) chloride In water; isopropyl alcohol for 3h; Stage #3: With water In isopropyl alcohol Product distribution / selectivity; |
1-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-5-(4-chlorophenylsulfonyl)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzene
ubidecarenone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: EtNH2; Li / tetrahydrofuran / 0.5 h / -78 °C 1.2: 86.1 percent / isoprene; NH4Cl / tetrahydrofuran 2.1: 93 percent / aq. HCl / methanol; hexane / 4 h / 40 °C View Scheme |
(tert-butyl){[(2E)-4-(3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylphenyl)-2-methylbut-2-enyl]oxy}dimethylsilane
ubidecarenone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 96.6 percent / Bu3NF*H2O / tetrahydrofuran / 0.67 h / 0 °C 2.1: 96.8 percent / MsCl; 2,6-dimethylpyridine; LiCl / dimethylformamide / 4 h / -5 °C 3.1: BuLi / hexane; tetrahydrofuran; hexamethylphosphoric acid triamide / 0.5 h / -70 °C 3.2: 75.8 percent / hexane; tetrahydrofuran; hexamethylphosphoric acid triamide / 3 h / -70 - 20 °C 4.1: EtNH2; Li / tetrahydrofuran / 0.5 h / -78 °C 4.2: 86.1 percent / isoprene; NH4Cl / tetrahydrofuran 5.1: 93 percent / aq. HCl / methanol; hexane / 4 h / 40 °C View Scheme |
ubidecarenone
Conditions | Yield |
---|---|
With ascorbic acid In ethanol; water at 50 - 78℃; for 30h; | 99.3% |
With ascorbic acid In ethanol at 78℃; for 30h; | 95% |
With ascorbic acid In ethanol at 78℃; for 30h; | 95% |
ubidecarenone
ubiquinol
Conditions | Yield |
---|---|
With sodium thiosulfate; sodium chloride In water at 48℃; for 2h; pH=4 - 6; | 99% |
With sodium thiosulfate; sodium chloride In n-heptane; water at 25℃; for 2h; pH=4 - 6; | 99% |
With sodium hydroxide; ascorbic acid In ethanol at 50℃; | 98% |
ubidecarenone
ubiquinone 8
Ubichinon-7
A
ubiquinol-8
B
ubiquinol
C
reduced coenzyme Q7
Conditions | Yield |
---|---|
With ascorbic acid In ethanol at 78℃; for 30h; | A 0.3% B 97% C 0.4% |
ubidecarenone
Conditions | Yield |
---|---|
With ascorbic acid In ethanol at 78℃; for 30h; | 95% |
ubidecarenone
mono(6-diethylenetriamino-6-deoxy)-β-cyclodextrin
C46H81N3O34*C59H90O4
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 20℃; for 72h; | 49% |
ubidecarenone
mono-6-deoxy-6-(2-aminoethylamino)-β-cyclodextrin
C44H76N2O34*C59H90O4
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 20℃; for 72h; | 48% |
ubidecarenone
6A-{{2-{{2-[(2-aminoethyl)amino]ethyl}amino}ethyl}amino}-6A-deoxy-β-cyclodextrin
C48H86N4O34*C59H90O4
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 20℃; for 72h; | 47% |
ubidecarenone
ubichromenol-9
Conditions | Yield |
---|---|
With triethylamine at 95℃; for 2h; | 45% |
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In toluene at 100℃; under 2250.23 Torr; for 3h; Solvent; Pressure; Temperature; Time; Autoclave; | A 17% B n/a C n/a D n/a |
ubidecarenone
diethoxy-CoQ10
Conditions | Yield |
---|---|
With sodium ethanolate |
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