We can offer products of different specifications Appearance:bottle Storage:-20℃ Application:Determination of corresponding toxins
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inquiryAs 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 according to the contract research and development services for the fine c
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inquiry1.In No Less 10 years exporting experience. you 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 Specializ
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inquiryZhenyu 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
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inquiry(?-ANATOXIN A FUMARATE; (?-2-ACETYL-9-AZA BICYCLO[4.2.1]NON-2-ENE FUMARATECASAppearance: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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inquiryChangzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
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inquiryhigh purity Application:Drug intermediates Materials intermediates and active molecules
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inquiry(+)-(1R)-2-acetyl-9-benzyloxycarbonyl-9-azabicyclo[4.2.1]-2-nonene
anatoxin-a
Conditions | Yield |
---|---|
With trimethylsilyl iodide In acetonitrile at -10℃; for 0.333333h; | 99% |
(-)-N-tosylanatoxin-a
anatoxin-a
Conditions | Yield |
---|---|
With disodium hydrogenphosphate; sodium amalgam In methanol at -40℃; for 0.166667h; | 76% |
(1R,6R)-2-Acetyl-9-aza-bicyclo[4.2.1]non-2-ene-9-carboxylic acid vinyl ester
anatoxin-a
Conditions | Yield |
---|---|
With hydrochloric acid diethyl ether In ethanol at 50℃; |
methyl (2R)-pyroglutamate
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: 100 percent / LiHMDS / tetrahydrofuran / -78 - 20 °C 2.1: Mg / tetrahydrofuran / 0.83 h / 20 °C 2.2: 73 percent / TMEDA / tetrahydrofuran / 1.5 h / -78 °C 3.1: BF3*OEt2; Ph3SiH / CH2Cl2 / 2.5 h / -78 - 20 °C 3.2: DIBAL-H / toluene / 3 h / -78 °C 3.3: 826 mg / Cs2CO3 / toluene; propan-2-ol / 17 h / 20 °C 4.1: 97 percent / NaHMDS / tetrahydrofuran / 2 h / -78 °C 5.1: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 6.1: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 7.1: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 8.1: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
1-benzyl 2-methyl (R)-5-oxopyrrolidine-1,2-dicarboxylate
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: Mg / tetrahydrofuran / 0.83 h / 20 °C 1.2: 73 percent / TMEDA / tetrahydrofuran / 1.5 h / -78 °C 2.1: BF3*OEt2; Ph3SiH / CH2Cl2 / 2.5 h / -78 - 20 °C 2.2: DIBAL-H / toluene / 3 h / -78 °C 2.3: 826 mg / Cs2CO3 / toluene; propan-2-ol / 17 h / 20 °C 3.1: 97 percent / NaHMDS / tetrahydrofuran / 2 h / -78 °C 4.1: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 5.1: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 6.1: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 7.1: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(2R,5R)-5-but-3-enyl-2-ethynylpyrrolidine-1-carboxylic acid 1-benzyl ester
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 97 percent / NaHMDS / tetrahydrofuran / 2 h / -78 °C 2: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 3: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 4: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 5: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(2R)-but-3-enyl-(5R)-prop-1-ynylpyrrolidine-1-carboxylic acid 1-benzyl ester
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 2: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 3: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 4: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(+)-(1R)-2-isopropenyl-9-benzyloxycarbonyl-9-azabicyclo[4.2.1]-2-nonene
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 2: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 3: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(2R)-benzyloxycarbonylamino-5-oxonon-8-enoic acid methyl ester
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: BF3*OEt2; Ph3SiH / CH2Cl2 / 2.5 h / -78 - 20 °C 1.2: DIBAL-H / toluene / 3 h / -78 °C 1.3: 826 mg / Cs2CO3 / toluene; propan-2-ol / 17 h / 20 °C 2.1: 97 percent / NaHMDS / tetrahydrofuran / 2 h / -78 °C 3.1: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 4.1: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 5.1: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 6.1: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(+)-(1R)-2-(1,2-dihydroxy-1-methylethyl)-9-benzyloxycarbonyl-9-azabicyclo[4.2.1]-2-nonene
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 2: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(2R)-but-3-enyl-(5R)-2-(1-methylsiletan-1-ylethynyl)pyrrolidine-1-carboxylic acid benzyl ester
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 9 percent / second generation Grubbs catalyst / CH2Cl2 / 80 °C 2: 97 percent / NaHMDS / tetrahydrofuran / 2 h / -78 °C 3: 84 percent / second generation Grubbs catalyst / CH2Cl2 / 16 h 4: 76 percent / Et3N; OsO4 / tetrahydrofuran / 22 h / -78 - 20 °C 5: 95 percent / NaIO4 / tetrahydrofuran; H2O / 1.5 h / 20 °C 6: 99 percent / TMSI / acetonitrile / 0.33 h / -10 °C View Scheme |
(1R)-9-methyl-9-azabicyclo[4.2.1]nonan-2-one
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: LiN(SiMe3)2 / tetrahydrofuran / -40 °C 2: 95 percent / K2CO3 / CH2Cl2 / Heating 3: AlCl3 / 1,2-dichloro-ethane / -10 °C 4: 65 percent / LiBr, Li2CO3 / dimethylformamide / 150 °C 5: HCl*Et2O / ethanol / 50 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 95 percent / K2CO3 / CH2Cl2 / Heating 2: AlCl3 / 1,2-dichloro-ethane / -10 °C 3: 65 percent / LiBr, Li2CO3 / dimethylformamide / 150 °C 4: HCl*Et2O / ethanol / 50 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 65 percent / LiBr, Li2CO3 / dimethylformamide / 150 °C 2: HCl*Et2O / ethanol / 50 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AlCl3 / 1,2-dichloro-ethane / -10 °C 2: 65 percent / LiBr, Li2CO3 / dimethylformamide / 150 °C 3: HCl*Et2O / ethanol / 50 °C View Scheme |
(-)-(5S)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}-1-tosylpyrrolidin-2-one
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1: 92 percent / DIBAL / CH2Cl2 / -78 °C 2: 87 percent / PPTS / methanol 3: 96 percent / Bu4NF / tetrahydrofuran 4: 1.) BuLi / 1.) THF, -78 deg C 5: toluene / Irradiation 6: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 7: 79 percent / NaH / tetrahydrofuran 8: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 9: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 12 steps 1: 92 percent / DIBAL / CH2Cl2 / -78 °C 2: 87 percent / PPTS / methanol 3: 96 percent / Bu4NF / tetrahydrofuran 4: 1.) BuLi / 1.) THF, -78 deg C 5: toluene / Irradiation 6: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 7: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 8: tetrahydrofuran 9: 76 percent / TiCl4 / CH2Cl2 / -78 °C 10: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 11: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 12: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
[(2S,5R)-5-Methoxy-1-(toluene-4-sulfonyl)-pyrrolidin-2-yl]-methanol
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 1.) BuLi / 1.) THF, -78 deg C 2: toluene / Irradiation 3: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 4: 79 percent / NaH / tetrahydrofuran 5: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 6: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 9 steps 1: 1.) BuLi / 1.) THF, -78 deg C 2: toluene / Irradiation 3: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 4: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 5: tetrahydrofuran 6: 76 percent / TiCl4 / CH2Cl2 / -78 °C 7: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 8: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 9: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
(2R,5R)-2-But-3-enyl-5-methoxy-1-(toluene-4-sulfonyl)-pyrrolidine
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 2: 79 percent / NaH / tetrahydrofuran 3: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 4: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 7 steps 1: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 2: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 3: tetrahydrofuran 4: 76 percent / TiCl4 / CH2Cl2 / -78 °C 5: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 6: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 7: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
(1R,6R)-9-(Toluene-4-sulfonyl)-2-vinyl-9-aza-bicyclo[4.2.1]nonane
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 2: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 3: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 79 percent / NaH / tetrahydrofuran 2: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 3: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
4-[(2R,5R)-5-Methoxy-1-(toluene-4-sulfonyl)-pyrrolidin-2-yl]-butan-1-ol
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 2: tetrahydrofuran 3: 76 percent / TiCl4 / CH2Cl2 / -78 °C 4: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 5: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 6: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 2: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: tetrahydrofuran 2: 76 percent / TiCl4 / CH2Cl2 / -78 °C 3: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 4: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 5: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
(E)-6-[(2R,5R)-5-Methoxy-1-(toluene-4-sulfonyl)-pyrrolidin-2-yl]-hex-3-en-2-one
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 2: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
(2R,5R)-2-Methoxy-1-(toluene-4-sulfonyl)-5-((E)-5-trimethylsilanyl-pent-4-enyl)-pyrrolidine
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 76 percent / TiCl4 / CH2Cl2 / -78 °C 2: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 3: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 4: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: toluene / Irradiation 2: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 3: 79 percent / NaH / tetrahydrofuran 4: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 5: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 8 steps 1: toluene / Irradiation 2: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 3: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 4: tetrahydrofuran 5: 76 percent / TiCl4 / CH2Cl2 / -78 °C 6: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 7: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 8: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
N-p-toluenesulphonyl(5-diphenyl-tert-butylsilyloxymethyl)-2-hydroxypyrrolidine
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1: 87 percent / PPTS / methanol 2: 96 percent / Bu4NF / tetrahydrofuran 3: 1.) BuLi / 1.) THF, -78 deg C 4: toluene / Irradiation 5: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 6: 79 percent / NaH / tetrahydrofuran 7: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 8: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 11 steps 1: 87 percent / PPTS / methanol 2: 96 percent / Bu4NF / tetrahydrofuran 3: 1.) BuLi / 1.) THF, -78 deg C 4: toluene / Irradiation 5: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 6: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 7: tetrahydrofuran 8: 76 percent / TiCl4 / CH2Cl2 / -78 °C 9: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 10: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 11: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
N-p-toluenesulphonyl(5-diphenyl-tert-butylsilyloxymethyl)-2-methoxypyrrolidine
anatoxin-a
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1: 96 percent / Bu4NF / tetrahydrofuran 2: 1.) BuLi / 1.) THF, -78 deg C 3: toluene / Irradiation 4: 1.) O3, 2.) Me2S / 1.) CH2Cl2, -78 deg C 5: 79 percent / NaH / tetrahydrofuran 6: 1.) HCl, 2.) DBU / 1.) CH2Cl2, MeOH, 2.) toluene, reflux 7: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme | |
Multi-step reaction with 10 steps 1: 96 percent / Bu4NF / tetrahydrofuran 2: 1.) BuLi / 1.) THF, -78 deg C 3: toluene / Irradiation 4: 1.) BH3*DMS, 2.) H2O2, 6M NaOH / 1.) THF 5: 1.) (COCl)2, 2.) Et3N / 1.) DMSO, 2.) CH2Cl2, -78 deg C 6: tetrahydrofuran 7: 76 percent / TiCl4 / CH2Cl2 / -78 °C 8: 71 percent / O2 / PdCl2, CuCl / dimethylformamide; H2O 9: 1.) KH, TMSCl, 2.) Et3N / 2.) Pd(OAc)2 / 2.) CH3CN 10: 76 percent / Na(Hg), Na2HPO4 / methanol / 0.17 h / -40 °C View Scheme |
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