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Qingdao Beluga Import and Export Co., LTD

CP 47497 CAS:70434-82-1 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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Henan Wentao Chemical Product Co., Ltd.

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Zibo Hangyu Biotechnology Development Co., Ltd

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Antimex Chemical Limied

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

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Wuhan Circle Star Chem-medical Technology co.,Ltd.

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We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as pri

rel-5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]phenol

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Hangzhou Fandachem Co.,Ltd

(?-CP 47497; REL-5-(1,1-DIMETHYLHEPTYL)-2-[(1R,3S)-3-HYDROXYCYCLOHEXYL]-PHENOLCASAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

(?-CP 47497; REL-5-(1,1-DIMETHYLHEPTYL)-2-[(1R,3S)-3-HYDROXYCYCLOHEXYL]-PHENOLCAS

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Henan Kanbei Chemical Co.,LTD

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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besold holdings plc

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Shanghai united Scientific Co.,Ltd.

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 innov

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Nanjing Raymon Biotech Co., Ltd.

CP 47,497;(C7)-CP 47,497 Top Drugs supplier Safe shipping Big stockAppearance:Solid Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,B

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Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the CP-47947, CAS:70434-82-1 with the most competitive price and the best quality. We can

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Wuxi Morality Chemical Co., Ltd

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(±)-CP 47497;rel-5-(1,1-DiMethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]phenol

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chem liyian

CAS number 70434-82-1 70434-92-3 (C8 homologue) Purity:99.8 PubChem CID 125835 Chemical data Formula C21H34O2 Mol. mass 318.492 g/mol …

rel-5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]phenol

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NovaChemistry

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(Z)-3-cyclohexanol

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rel-5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]phenol

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rel-5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]phenol

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Synthetic route

: 70434-49-0
(Z)-3-<2-(benzyloxy)-4-(1,1-dimethylheptyl)phenyl>cyclohexanol

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal In ethanol under 760 Torr; for 2h;	77%
With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal

: 930-68-7
cyclohexenone

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: CuI / tetrahydrofuran / 0.5 h / -3 °C 2: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 3: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme
Multi-step reaction with 3 steps 1: (i) Mg, (ii) CuI, (iii) /BRN= 1280477/ 2: sodium tetrahydroborate 3: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme
Multi-step reaction with 3 steps 1: (i) Mg, (ii) CuI, (iii) /BRN= 1280477/ 2: sodium tetrahydroborate 3: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme

: 70120-16-0
1-bromo-2-benzyloxy-4-(1,1-dimethylheptyl)benzene

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: Mg / tetrahydrofuran / 20 h / Heating 2: CuI / tetrahydrofuran / 0.5 h / -3 °C 3: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 4: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme
Multi-step reaction with 3 steps 1: (i) Mg, (ii) CuI, (iii) /BRN= 1280477/ 2: sodium tetrahydroborate 3: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme
Multi-step reaction with 3 steps 1: (i) Mg, (ii) CuI, (iii) /BRN= 1280477/ 2: sodium tetrahydroborate 3: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme

: 70434-13-8
3-<2-(benzyloxy)-4-(1,1-dimethylheptyl)phenyl>cyclohexanone

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 2: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme
Multi-step reaction with 2 steps 1: sodium tetrahydroborate 2: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme
Multi-step reaction with 2 steps 1: sodium tetrahydroborate 2: hydrogen; sodium hydrogencarbonate / palladium on activated charcoal View Scheme

: 70120-12-6
2-(3-hydroxyphenyl)-2-methyloctane

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C 2: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 3: Mg / tetrahydrofuran / 20 h / Heating 4: CuI / tetrahydrofuran / 0.5 h / -3 °C 5: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 6: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

: 70120-14-8
2-(4-bromo-3-hydroxyphenyl)-2-methyloctane

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 2: Mg / tetrahydrofuran / 20 h / Heating 3: CuI / tetrahydrofuran / 0.5 h / -3 °C 4: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 5: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

: 70120-09-1
2-(3-benzyloxyphenyl)-2-methylpropionaldehyde

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 8 steps 1: 57 percent / DMSO, NaOH / 4 h / 15 °C 2: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr 3: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C 4: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 5: Mg / tetrahydrofuran / 20 h / Heating 6: CuI / tetrahydrofuran / 0.5 h / -3 °C 7: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 8: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

Yield

Multi-step reaction with 8 steps
1: 57 percent / DMSO, NaOH / 4 h / 15 °C
2: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr
3: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C
4: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min
5: Mg / tetrahydrofuran / 20 h / Heating
6: CuI / tetrahydrofuran / 0.5 h / -3 °C
7: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C
8: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr
View Scheme

: 70120-08-0
2-<3-(benzyloxy)phenyl>-2-methylpropionitrile

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 9 steps 1: 1.) diisobutylaluminium hydride (DIBAL), 2.) aq. H2SO4 / 1.) THF, hexane, 25 deg C, 2 h, 2.) THF, hexane, 25 deg C, 2 h 2: 57 percent / DMSO, NaOH / 4 h / 15 °C 3: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr 4: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C 5: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 6: Mg / tetrahydrofuran / 20 h / Heating 7: CuI / tetrahydrofuran / 0.5 h / -3 °C 8: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 9: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

Yield

Multi-step reaction with 9 steps
1: 1.) diisobutylaluminium hydride (DIBAL), 2.) aq. H2SO4 / 1.) THF, hexane, 25 deg C, 2 h, 2.) THF, hexane, 25 deg C, 2 h
2: 57 percent / DMSO, NaOH / 4 h / 15 °C
3: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr
4: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C
5: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min
6: Mg / tetrahydrofuran / 20 h / Heating
7: CuI / tetrahydrofuran / 0.5 h / -3 °C
8: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C
9: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr
View Scheme

: 70120-10-4
1-(benzyloxy)-3-(1,1-dimethyl-2-heptenyl)benzene

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 7 steps 1: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr 2: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C 3: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 4: Mg / tetrahydrofuran / 20 h / Heating 5: CuI / tetrahydrofuran / 0.5 h / -3 °C 6: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 7: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

Yield

Multi-step reaction with 7 steps
1: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr
2: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C
3: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min
4: Mg / tetrahydrofuran / 20 h / Heating
5: CuI / tetrahydrofuran / 0.5 h / -3 °C
6: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C
7: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr
View Scheme

: 21406-61-1
pentyltriphenylphosphonium bromide

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 8 steps 1: 57 percent / DMSO, NaOH / 4 h / 15 °C 2: 78 percent / H2 / 10percent Pd/C / ethanol / 13 h / 2585.7 Torr 3: 100 percent / Br2 / CCl4 / 0.25 h / 30 °C 4: 1.) KH / 1.) DMF, -18 deg C, 15 min, 2.) 25 deg C, 30 min 5: Mg / tetrahydrofuran / 20 h / Heating 6: CuI / tetrahydrofuran / 0.5 h / -3 °C 7: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 8: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

Yield

: C22H29BrMgO

: 70434-82-1
(Z)-3-<4-(1,1-dimethylheptyl)-2-hydroxyphenyl>cyclohexanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: CuI / tetrahydrofuran / 0.5 h / -3 °C 2: 51 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / -40 °C 3: 77 percent / H2, NaHCO3 / 10percent Pd/C / ethanol / 2 h / 760 Torr View Scheme

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