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 ch
1. 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
Cas:502-61-4
Min.Order:1 Gram
FOB Price: $0.1
Type:Manufacturers
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
Our Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
Cas:502-61-4
Min.Order:10 Kilogram
Negotiable
Type:Trading Company
inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
Cas:502-61-4
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryFARNESENE CAS:502-61-4 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, st
Cas:502-61-4
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:502-61-4
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Cas:502-61-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Zibo Hangyu Biotechnology Development 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 chemi
We are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Our Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
Cas:502-61-4
Min.Order:1 bottle
Negotiable
Type:Lab/Research institutions
inquiryTAIHO Unique Advantages:1.We're factory2.Free samples available3.Commodity inspection can be done4.ISO9001,Kosher certifications5.10 years experiences Storage:Store in cool &dry place Package:aluminium foil bag/fiber can/plastic drum Application:comp
Cas:502-61-4
Min.Order:0
Negotiable
Type:Manufacturers
inquiryJ&H CHEM is one of China's leading providers of integrated fine chemical services including offering, research and development, Custom manufacturing business, as well as other Value-added customer services, for diversified range products of chemicals
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Cas:502-61-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquirybest seller Application:API
1,we produce and sell good chemicals around the world.2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%.3,our staff consists of highly qualified in
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Cas:502-61-4
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryFarnesene Application:Farnesene
Appearance:solid or liquid Storage:sealed in cool and dry place Package:As customer's requested Application:Pharma Intermediate Transportation:by courier/air/sea Port:Any port in China
best seller Application:API
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
1. Timely and efficient service to ensure communication with customers2. Produce products of different specifications and sizes according to your requirements.3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures sta
(2'E)-2-(3',7'-dimethylocta-2',6'-dienyl)-3-methyl-2,5-dihydrothiophen 1,1-dioxide
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
In xylene for 0.0833333h; Heating; | 93% |
In xylene Heating; | 83% |
With pyridine at 150℃; for 3h; Inert atmosphere; | 80% |
Multi-step reaction with 4 steps 1: 1.) H2O, NBS, 2.) K2CO3 / 1.) THF, 0 deg C, 1 h, 2.) MeOH 2: 73 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 3: 78.3 percent / xylene / 0.08 h / Heating 4: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme | |
Multi-step reaction with 4 steps 1: 1.) H2O, NBS, 2.) K2CO3 / 1.) THF, 0 deg C, 1 h, 2.) MeOH 2: 92 percent / xylene / 0.08 h / Heating 3: 42 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 4: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme |
(E)-3,7,11-trimethyl-1,6,10-dodecatrien-3-ol
A
(E)-β-farnesene
B
(3Z,6E)-α-farnesene
C
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With pyridine In dimethyl sulfoxide at 160℃; for 0.0833333h; | A 29% B 36% C 17% |
With trichlorophosphate In dimethyl sulfoxide at 160℃; for 0.0833333h; | A 29% B 36% C 17% |
With pyridine; trichlorophosphate In dimethyl sulfoxide at 160℃; for 0.0833333h; | A 29% B 36% C 17% |
With pyridine; trichlorophosphate |
(E)-β-farnesene
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
rhodium(II) chloride In ethanol |
Conditions | Yield |
---|---|
rhodium(II) chloride In ethanol |
Farnesol
A
(E)-β-farnesene
B
(E,E)-alpha-farnesene
C
(Z)-γ-bisabolene
D
β-bisabolene
Conditions | Yield |
---|---|
With potassium hydrogensulfate |
(E)-3,7,11-trimethyl-1,6,10-dodecatrien-3-ol
A
(E)-β-farnesene
B
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With dimethyl sulfoxide Heating; |
(3E,6E)-3,7,11-trimethyl-dodeca-3,6,10-triene-1,2-diol
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
(i) PBr3, CuBr, Et2O, (ii) Zn; Multistep reaction; | |
(i) CuBr, PBr3, (ii) Zn; Multistep reaction; |
phosphoric acid diphenyl ester (2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
In diethyl ether |
(2Ξ,5Z)-2,6,10-trimethyl-undeca-2,5,9-trienal
Methylenetriphenylphosphorane
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 40℃; for 3h; |
3-buten-1-yne
trimethylaluminum
1-chloro-3,7-dimethylocta-2,6-diene
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); zirconocene dichloride 1.) 1,2-dichloroethane, xylene, room temperature, 12 h, 2.) THF, room temperature, 3 h; Yield given. Multistep reaction; |
isopropyltriphenylphosphonium iodide
4,8-dimethyldeca-4E,7E,9-trienal
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With n-butyllithium 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min; Yield given. Multistep reaction; |
A
(3Z,6E)-α-farnesene
B
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 50℃; for 0.0833333h; Yield given. Yields of byproduct given; |
A
(3Z,6E)-α-farnesene
B
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide Yield given; |
A
(3Z,6E)-α-farnesene
B
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide Yield given; |
(+/-)-nerolidol
A
(E)-β-farnesene
B
(E,E)-alpha-farnesene
C
(Z)-beta-Farnesene
D
(Z,Z)-α-farnesene
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate 1) ice bath, 1 h; 2) rt, 12 h; Title compound not separated from byproducts; |
farnesyl pyrophosphate
A
(E)-β-farnesene
B
(E,E)-alpha-farnesene
C
[E]-γ-bisabolene
D
γ-curcumene
Conditions | Yield |
---|---|
With taxadiene synthase In phosphate buffer at 30℃; Product distribution; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Dowex 50W-X4 cation exchange resin In hexane for 4h; Heating; | |
Multi-step reaction with 2 steps 1: KHSO4 2: RhCl2 / ethanol View Scheme | |
Multi-step reaction with 2 steps 1: KHSO4 2: RhCl2 / ethanol View Scheme | |
Multi-step reaction with 2 steps 1: (i) VO(acac)2, tBuO2H, benzene, (ii) Me3SiCl, hexamethyldisilazane, Py, (iii) diethylaluminium 2,2,6,6-tetramethyl-piperidide, (iv) KF, aq. MeOH 2: (i) PBr3, CuBr, Et2O, (ii) Zn View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 72 percent / BuLi / hexane; diethyl ether / 1.) 20 deg C, 15 min, 2.) -78 deg C, 30 min; r.t., 30 min 2: LDA / diethyl ether / 1.) 0 deg C, 30 min, 2.) -78 deg C, 30 min; 25 deg C, 30 min 3: NaH / dimethylformamide View Scheme | |
Multi-step reaction with 3 steps 1: 72 percent / BuLi / hexane; diethyl ether / 1.) 20 deg C, 15 min, 2.) -78 deg C, 30 min; r.t., 30 min 2: LDA / diethyl ether / 1.) 0 deg C, 30 min, 2.) -78 deg C, 30 min; 25 deg C, 30 min 3: NaH / dimethylformamide View Scheme | |
Multi-step reaction with 2 steps 1: 1.) BuLi 2: 83 percent / xylene / Heating View Scheme |
1-(Diphenylphosphinyl)-4,8-dimethyl-3,7-nonadiene
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: LDA / diethyl ether / 1.) 0 deg C, 30 min, 2.) -78 deg C, 30 min; 25 deg C, 30 min 2: NaH / dimethylformamide View Scheme | |
Multi-step reaction with 2 steps 1: LDA / diethyl ether / 1.) 0 deg C, 30 min, 2.) -78 deg C, 30 min; 25 deg C, 30 min 2: NaH / dimethylformamide View Scheme |
10,11-epoxy-3,7,11-trimethyldodeca-1,3E,6E-triene
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 42 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 2: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme |
2-3'-methyl-6'-oxohexa-2'E-enyl-3-methyl-2,5-dihydrothiophene-1,1-dioxide
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min 2: 93 percent / xylene / 0.08 h / Heating View Scheme | |
Multi-step reaction with 5 steps 1: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min 2: 1.) H2O, NBS, 2.) K2CO3 / 1.) THF, 0 deg C, 1 h, 2.) MeOH 3: 92 percent / xylene / 0.08 h / Heating 4: 42 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 5: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme | |
Multi-step reaction with 2 steps 1: 78.3 percent / xylene / 0.08 h / Heating 2: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme |
2-Methyl-3-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ6-thiophen-2-ylmethyl)-2-(4-methyl-pent-3-enyl)-oxirane
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 73 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 2: 78.3 percent / xylene / 0.08 h / Heating 3: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme |
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 92 percent / xylene / 0.08 h / Heating 2: 42 percent / periodic acid / tetrahydrofuran / 0.03 h / Ambient temperature 3: 1.) n-BuLi / 1.) THF, pentane, RT, 2.) THF, pentane, -78 deg C, 15 min View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) BuLi 2: 83 percent / xylene / Heating View Scheme |
2-((Z)-3,7-dimethyl-octa-2,6-dienyl)-[1,3]dioxolane
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: TsOH / acetone; H2O / 4 h / Ambient temperature 2: (i) NaH, diglyme, (ii) /BRN= 2238274/ 3: LiAlH4 / diethyl ether / 2 h / Ambient temperature 4: MnO2 / petroleum ether / 8 h 5: dimethylsulfoxide / 3 h / 40 °C View Scheme |
(E)-3,7,11-trimethyl-1,6,10-dodecatrien-3-ol
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: KOH 2: RhCl2 / ethanol View Scheme | |
Multi-step reaction with 2 steps 1: KOH 2: RhCl2 / ethanol View Scheme |
(Z)-4,8-dimethylnona-3,7-dienal
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: (i) NaH, diglyme, (ii) /BRN= 2238274/ 2: LiAlH4 / diethyl ether / 2 h / Ambient temperature 3: MnO2 / petroleum ether / 8 h 4: dimethylsulfoxide / 3 h / 40 °C View Scheme |
(2Ξ,5Z)-2,6,10-trimethyl-undeca-2,5,9-trien-1-ol
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: MnO2 / petroleum ether / 8 h 2: dimethylsulfoxide / 3 h / 40 °C View Scheme |
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: LiAlH4 / diethyl ether / 2 h / Ambient temperature 2: MnO2 / petroleum ether / 8 h 3: dimethylsulfoxide / 3 h / 40 °C View Scheme |
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) diethylaluminium 2,2,6,6-tetramethyl-piperidide, benzene, (ii) KF, aq. MeOH 2: (i) CuBr, PBr3, (ii) Zn View Scheme |
(E,E)-alpha-farnesene
ethyl acetoacetate
(4E,8E)-ethyl 2-acetyl-5,9,13-trimethyltetradeca-4,8,12-trienoate
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triphenylphosphine at 50℃; for 24h; Temperature; Large scale; | 94% |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triphenylphosphine In ethanol at 70℃; for 15h; Large scale; | 93% |
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; carbonyl(pentamethylcyclopentadienyl)cobalt diiodide; acetic acid In 1,4-dioxane at 50℃; for 16h; | 63% |
(E,E)-alpha-farnesene
B
10,11-epoxy-3,7,11-trimethyldodeca-1,3E,6E-triene
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In dichloromethane Ambient temperature; | A 11% B 31% C 2% D 1% |
With sodium acetate; 3-chloro-benzenecarboperoxoic acid In dichloromethane 1.) 0 deg C, 15 min, 2.) 1 h; Further byproducts given; | A n/a B 20% C n/a D n/a |
(E,E)-alpha-farnesene
B
(-)-(3E,6E,10S)-3,7,11-trimethyldodeca-1,3,6-triene-10,11-diol
C
(-)-(3E,6S,7S,10S)-3,7,11-trimethyldodeca-1,3-diene-6,7,10,11-triol
Conditions | Yield |
---|---|
With (3a,9R,3'''a,4'"b,9'"R)-9,9'-[1,4-phthalazinediylbis(oxy)]bis[6'-(methyloxy)-10,11-dihydrocinchonan]; osmium(VIII) oxide; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) at 0℃; for 6h; Product distribution; with other phthalazines; | A 28% B 11% C 7% |
With (3a,9R,3'''a,4'"b,9'"R)-9,9'-[1,4-phthalazinediylbis(oxy)]bis[6'-(methyloxy)-10,11-dihydrocinchonan]; osmium(VIII) oxide; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) at 0℃; for 6h; | A 28% B 11% C 7% |
(E,E)-alpha-farnesene
Conditions | Yield |
---|---|
With sodium acetate; 3-chloro-benzenecarboperoxoic acid In dichloromethane 1.) 0 deg C, 15 min, 2.) 1 h; | A 9% B 19% |
(E,E)-alpha-farnesene
B
(+)-(3E,6E,10R)-3,7,11-trimethyldodeca-1,3,6-triene-10,11-diol
C
(+)-(3E,6R,7R,10R)-3,7,11-trimethyldodeca-1,3-diene-6,7,10,11-tetraol
Conditions | Yield |
---|---|
With (3a,9R,3'''a,4'"b,9'"R)-9,9'-[1,4-phthalazinediylbis(oxy)]bis[6'-(methyloxy)-10,11-dihydrocinchonan]; osmium(VIII) oxide; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) at 0℃; for 6h; | A 18% B 15% C 14% |
(E,E)-alpha-farnesene
B
(+)-(3E,6E,10R)-3,7,11-trimethyldodeca-1,3,6-triene-10,11-diol
C
(+)-(3E,6R,7R,10R)-3,7,11-trimethyldodeca-1,3-diene-6,7,10,11-tetraol
Conditions | Yield |
---|---|
With osmium(VIII) oxide; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yields of byproduct given; | A n/a B 15% C n/a D n/a |
With osmium(VIII) oxide; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yields of byproduct given; | A n/a B n/a C 14% D n/a |
With osmium(VIII) oxide; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
(E,E)-alpha-farnesene
B
(-)-(3E,6E,10S)-3,7,11-trimethyldodeca-1,3,6-triene-10,11-diol
C
(-)-(3E,6S,7S,10S)-3,7,11-trimethyldodeca-1,3-diene-6,7,10,11-triol
Conditions | Yield |
---|---|
With osmium(VIII) oxide; methanesulfonamide; potassium carbonate; hydroquinidein 1,4-phthalazinediyl diether; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yields of byproduct given; | A n/a B 11% C n/a D n/a |
With osmium(VIII) oxide; (DHQ)2-PHAL; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yields of byproduct given; | A n/a B n/a C 7% D n/a |
With osmium(VIII) oxide; (DHQ)2-PHAL; methanesulfonamide; potassium carbonate; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 0℃; for 6h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
(E,E)-alpha-farnesene
B
10,11-epoxy-3,7,11-trimethyldodeca-1,3E,6E-triene
Conditions | Yield |
---|---|
With 3,3-dimethyldioxirane In dichloromethane for 1h; | A 5% B 7% C 9% |
Conditions | Yield |
---|---|
With 3,5-dimethyl-1H-pyrazole; chromium(VI) oxide In dichloromethane for 2h; | 6% |
(E,E)-alpha-farnesene
acetic anhydride
[(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate
Conditions | Yield |
---|---|
With manganese triacetate In acetic acid for 1.5h; Heating; | 4% |
(E,E)-alpha-farnesene
2,6,10-trimethyldodeca-2,6,9,11-tetraen-1-ol
Conditions | Yield |
---|---|
With selenium(IV) oxide In ethanol at 80℃; for 0.333333h; Product distribution; other oxidizers (photooxidizers) and products; | 3% |
With selenium(IV) oxide In ethanol at 80℃; for 0.333333h; | 3% |
(E,E)-alpha-farnesene
A
2,6,10-trimethyldodeca-2,6,9,11-tetraen-1-ol
Conditions | Yield |
---|---|
With selenium(IV) oxide; 4-methylmorpholine N-oxide In methanol; dichloromethane for 6h; Heating; | A 1% B 1% |
Conditions | Yield |
---|---|
(i) (irradiation), (ii) Na, EtOH; Multistep reaction; |
(E,E)-alpha-farnesene
(3Z,6E)-α-farnesene
Conditions | Yield |
---|---|
In benzene Irradiation; |
(E,E)-alpha-farnesene
3,7,11-trimethyldodeca-1,3(E),5(E),10-tetraen-7-ol
Conditions | Yield |
---|---|
(i) eosine, O2, EtOH, (ii) NaBH4, (iii) H2O; Multistep reaction; |
(E,E)-alpha-farnesene
(E)-3,11-dimethyl-7-methylene-dodeca-1,3,10-trien-6-ol
Conditions | Yield |
---|---|
(i) eosine, O2, EtOH, (ii) NaBH4, (iii) H2O; Multistep reaction; |
(E,E)-alpha-farnesene
3,7-dimethyl-11-methylenedodeca-1,3,6-trien-10-ol
Conditions | Yield |
---|---|
(i) eosine, O2, EtOH, (ii) NaBH4, (iii) H2O; Multistep reaction; |
(E,E)-alpha-farnesene
3,7,11-trimethyldodeca-1,3,6,9-tetraen-11-ol
Conditions | Yield |
---|---|
(i) eosine, O2, EtOH, (ii) NaBH4, (iii) H2O; Multistep reaction; |
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