SL0101 CAS:77307-50-7 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:77307-50-7
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
Henan 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
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
Cas:77307-50-7
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiry1.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.
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
GMP factory Packing with pallet as buyer's special request Best service after shipment with e-mail Cargos together with container sales seervice available Api, inhibitor, and fine chemicals for more than 6 years. Application:
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
Joyinchem have been committed to chemical supply for several years and have built good cooperation records with multinational chemical corporations and importers from all over the world. Our services include:-Spot goods-Contract manufacturing-Custom
SL0101Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fed
1 good quality, better price and bettter service;2 Timely delivery;3 100% refunded if parcel is t delivered or poor quality.We will try to satisfy you upon receipt of your reply. I hope that we can become a long-term cooperative partner. Application:
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the SL0101, CAS:77307-50-7 with the most competitive price and the best quality. We can o
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Cas:77307-50-7
Min.Order:0
Negotiable
Type:Other
inquiryShanghai Caerulum Pharma Discovery was established in 2012 as an integrated CRO (Contract Research Organization), providing professional chemical services. As a customer-oriented company, Caerulum Pharma Discovery has distinguished itself from others
Cas:77307-50-7
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
inquirySL0101Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them from sunshine o
5,7-bis(benzyloxy)-2-(4-benzyloxyphenyl)-3-[3,4-di-O-acetyl-2-O-benzyl-α-L-rhamnopyranosyloxy]-4H-chromen-4-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
With hydrogen; palladium dihydroxide In tetrahydrofuran; methanol for 1h; | 94% |
With hydrogen; palladium hydroxide on carbon In tetrahydrofuran; methanol for 1h; | 94% |
(2S,3S,4S,5R,6S)-6-((5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4-oxo-4H-chromen-3- yl)oxy)-5-hydroxy-2-methyltetrahydro-2H-pyran-3,4-diyl diacetate
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 0℃; for 1h; | 91% |
tert-butyl ((2S,6S)-6-methyl-5-oxo-5,6-dihydro-2H-pyran-2-yl) carbonate
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 2.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 3.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 4.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 5.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 5.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 6.1: 62 percent / DBU / toluene / 1 h / 0 °C 7.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-3-hydroxy-4H-chromen-4-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 2.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 3.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 4.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 5.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 5.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 6.1: 62 percent / DBU / toluene / 1 h / 0 °C 7.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme | |
Multi-step reaction with 2 steps 1: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 2: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
3-((2S,6S)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yloxy)-5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4H-chromen-4-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 2.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 3.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 4.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 4.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 5.1: 62 percent / DBU / toluene / 1 h / 0 °C 6.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
3-((2S,5R,6S)-5,6-dihydro-5-hydroxy-6-methyl-2H-pyran-2-yloxy)-5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4H-chromen-4-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 2.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 3.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 3.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 4.1: 62 percent / DBU / toluene / 1 h / 0 °C 5.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
6-(5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4-oxo-4H-chromen-3-yloxy)-3,6-dihydro-2-methyl-2H-pyran-3-yl acetate
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 2.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 2.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 3.1: 62 percent / DBU / toluene / 1 h / 0 °C 4.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
(2S,3R,4S,5R,6S)-6-((5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4-oxo-4H-chromen-3-yl)oxy)-4,5-dihydroxy-2-methyltetrahydro-2H-pyran-3-yl acetate
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 1.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 2.1: 62 percent / DBU / toluene / 1 h / 0 °C 3.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
(2S,3R,4R,5R,6S)-2-((5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4-oxo-4H-chromen-3-yl)oxy)-4-hydroxy-6-methyltetrahydro-2H-pyran-3,5-diyl diacetate
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 62 percent / DBU / toluene / 1 h / 0 °C 2: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
1-(2-furyl)-1-ethanone
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 10 steps 1.1: 92 percent / formic acid; Et3N / (R)-Ru(η6-mesitylene)-(S,S)-TsDPEN / CH2Cl2 / 24 h / 20 °C 2.1: 90 percent / NaHCO3; NaOAc*3H2O; NBS / tetrahydrofuran; H2O / 1 h / 0 °C 3.1: 60 percent / DMAP / CH2Cl2 / 12 h / -78 °C 4.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 5.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 6.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 7.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 8.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 8.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 9.1: 62 percent / DBU / toluene / 1 h / 0 °C 10.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
5,7-bis(benzyloxy)-2-(4-(benzyloxy)phenyl)-4H-chromen-4-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: DMSO; 3 Angstroem molecular sieves / acetone; CH2Cl2 / -20 - 0 °C 1.2: 50 percent / TsOH*H2O / CH2Cl2 / 1 h / 20 °C 2.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 3.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 4.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 5.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 6.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 6.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 7.1: 62 percent / DBU / toluene / 1 h / 0 °C 8.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: DMDO / CH2Cl2; acetone / 0 °C 1.2: 78 percent Turnov. / pTsOH / CH2Cl2 / 0.5 h / 0 °C 2.1: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 3.1: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
5,7-Dihydroxy-2-(4-hydroxy-phenyl)-chroman-4-on
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 10 steps 1.1: 75 percent / K2CO3 / acetone / 6 h / Heating 2.1: 76 percent / I2 / dimethylsulfoxide / 24 h / 110 °C 3.1: DMSO; 3 Angstroem molecular sieves / acetone; CH2Cl2 / -20 - 0 °C 3.2: 50 percent / TsOH*H2O / CH2Cl2 / 1 h / 20 °C 4.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 5.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 6.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 7.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 8.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 8.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 9.1: 62 percent / DBU / toluene / 1 h / 0 °C 10.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
L-aculose
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: 60 percent / DMAP / CH2Cl2 / 12 h / -78 °C 2.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 3.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 4.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 5.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 6.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 6.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 7.1: 62 percent / DBU / toluene / 1 h / 0 °C 8.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
(S)-1-(2-furanyl)ethanol
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1.1: 90 percent / NaHCO3; NaOAc*3H2O; NBS / tetrahydrofuran; H2O / 1 h / 0 °C 2.1: 60 percent / DMAP / CH2Cl2 / 12 h / -78 °C 3.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 4.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 5.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 6.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 7.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 7.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 8.1: 62 percent / DBU / toluene / 1 h / 0 °C 9.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme |
(E)-1-(2,4-bis(benzyloxy)-6-hydroxyphenyl)-3-(4-(benzyloxy)phenyl)prop-2-en-1-one
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1.1: 76 percent / I2 / dimethylsulfoxide / 24 h / 110 °C 2.1: DMSO; 3 Angstroem molecular sieves / acetone; CH2Cl2 / -20 - 0 °C 2.2: 50 percent / TsOH*H2O / CH2Cl2 / 1 h / 20 °C 3.1: 85 percent / PPh3 / Pd2(dba)3*CHCl3 / CH2Cl2 / 3 h / 0 °C 4.1: 73 percent / NaBH4 / CH2Cl2; methanol / 3 h / -78 °C 5.1: 156 mg / pyridine; DMAP / CH2Cl2 / 1 h / 0 °C 6.1: 77 percent / OsO4; NMO / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C 7.1: p-TsOH*H2O / CH2Cl2 / 0.25 h / 0 °C 7.2: 99 percent / aq. HOAc / CH2Cl2 / 0.25 h / 0 °C 8.1: 62 percent / DBU / toluene / 1 h / 0 °C 9.1: 91 percent / DBU / toluene / 1 h / 0 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: 72 percent / I2 / dimethylsulfoxide / 140 °C 2.1: DMDO / CH2Cl2; acetone / 0 °C 2.2: 78 percent Turnov. / pTsOH / CH2Cl2 / 0.5 h / 0 °C 3.1: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 4.1: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
phenyl 2-O-benzyl-1-thio-α-L-rhamnopyranoside
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 100 percent / Et3N; DMAP / CH2Cl2 / 20 °C 2: 84 percent / Br2 / CH2Cl2 / 1 h / 0 °C 3: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 4: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
3,4-di-O-acetyl-2-O-benzyl-α-L-rhamnopyranosyl bromide
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 2: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
phenyl 3,4-di-O-acetyl-2-O-benzyl-1-thio-α-L-rhamnopyranoside
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 84 percent / Br2 / CH2Cl2 / 1 h / 0 °C 2: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 3: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
naringenin
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 81 percent / K2CO3 / acetone / Heating 2.1: 72 percent / I2 / dimethylsulfoxide / 140 °C 3.1: DMDO / CH2Cl2; acetone / 0 °C 3.2: 78 percent Turnov. / pTsOH / CH2Cl2 / 0.5 h / 0 °C 4.1: 60 percent / Ag2O / CH2Cl2 / 4 h / 20 °C 5.1: 94 percent / H2 / Pd(OH)2/C / tetrahydrofuran; methanol / 1 h View Scheme |
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran |
acetic anhydride
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Conditions | Yield |
---|---|
With pyridine at 23℃; for 1h; |
acetic anhydride
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
Peracetylated-SL0101
Conditions | Yield |
---|---|
With pyridine |
Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside)
kaempferol 3-rhamnoside
Conditions | Yield |
---|---|
With sodium hydroxide In methanol at 23℃; for 0.333333h; | 9 mg |
With potassium carbonate In methanol |
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