CAS No.160168-89-8,Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (5S)- (9CI) Suppliers

Hebei Nengqian Chemical Import and Export Co., LTD

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Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (5S)- (9CI)

Cas:160168-89-8

Min.Order:1 Kilogram

FOB Price: $1.0 / 10.0

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Zibo Hangyu Biotechnology Development Co., Ltd

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

Cyclohexanone,2-methyl-5-(1-methylethyl)-, (5S)-

Cas:160168-89-8

Min.Order:10 Gram

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Type:Lab/Research institutions

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

Zhenyu 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

Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (5S)- (9CI)

Cas:160168-89-8

Min.Order:1 Kilogram

FOB Price: $2.0

Type:Lab/Research institutions

inquiry

Xi`an Eastling Biotech Co., Ltd.

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou

Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (5S)- (9CI)

Cas:160168-89-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

factory?direct?sale Application:healing drugs

Cyclohexanone,2-methyl-5-(1-methylethyl)-, (5S)-

Cas:160168-89-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Synthetic route

: 2244-16-8, 6485-40-1
(S)-p-mentha-6,8-dien-2-one

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
With Rh/Al2O3; hydrogen In ethanol at 20℃; under 31503.2 Torr; for 3.5h; Autoclave;	99%
With 10% palladium on carbon; hydrogen	97%
With hydrogen; Lindlar's catalyst In ethanol
Multi-step reaction with 2 steps 1.1: water; potassium hydroxide; zinc / methanol / 73 h / Reflux 2.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 48 h / 20 °C 2.2: 0.33 h / 0 °C View Scheme

: 201012-68-2
(5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen In hexane at 20℃; under 11251.1 Torr; for 12h; Sealed tube; Inert atmosphere;	98.9%
Stage #1: (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one With palladium 10% on activated carbon; hydrogen In ethyl acetate at 20℃; for 48h; Stage #2: With Jones reagent In ethyl acetate at 0℃; for 0.333333h; Jones oxidation;	39.39 g

: 5745-59-5
(-)-1-hydroxyneoisocarvomenthol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
With sulfuric acid Heating;

: 6711-53-1
(-)-1-hydroxyisocarvomenthol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
With sulfuric acid

: 39904-00-2
(1R,2S,4S)-4-isopropyl-1-methylcyclohexane-1,2-diol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
With sulfuric acid

: Acetic acid (S)-5-isopropyl-2-methyl-cyclohex-1-enyl ester

A: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

B: 127911-15-3
(5R)-5-isopropyl-2-methylcyclohexanone

Conditions

Conditions	Yield
With cultured cells of Marchantia polymorpha; water at 25℃; for 5h; Yields of byproduct given. Title compound not separated from byproducts;

: 39903-99-6
(1R,2S,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: H2 / Raney-Ni / ethanol 2: aq. H2SO4 View Scheme

: 39904-04-6
(1S,2S,4S)-limonene glycol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: H2 / Raney-Ni / ethanol 2: aq. H2SO4 / Heating View Scheme

: 39904-01-3
(1S,2R,4S)-p-menth-8-ene-1,2-diol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: H2 / Raney-Ni / ethanol 2: aq. H2SO4 View Scheme

: 39903-74-7
(1S,2S,3R,5R)-2,3-epoxy-5-isopropenyl-2-methylcyclohex-2-enol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: LiAlH4 2: H2 / Raney-Ni / ethanol 3: aq. H2SO4 View Scheme

: (1R,2S,4R,6S)-4-Isopropenyl-1-methyl-7-oxa-bicyclo[4.1.0]heptan-2-ol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: LiAlH4 / diethyl ether 2: H2 / Raney-Ni / ethanol 3: aq. H2SO4 / Heating View Scheme

: 39903-82-7
(1R,2R,4R,6S)-4-isopropenyl-1-methyl-7-oxabicyclo[4.1.0]heptan-2-ol

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: LiAlH4 2: H2 / Raney-Ni / ethanol 3: aq. H2SO4 View Scheme

: 2244-16-8, 6485-40-1
(S)-p-mentha-6,8-dien-2-one

A: 499-71-8
carvotanacetone

B: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

C: 201012-68-2
(5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one

Conditions

Conditions	Yield
With hydrogen In tetrahydrofuran; water at 20℃; under 759.826 Torr; for 48h; Schlenk technique; Inert atmosphere;

...Expand

: 75-77-4
chloro-trimethyl-silane

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

: 1309660-00-1
1-[(5S)-2-methyl-5-(methylethyl)cyclohex-1-enyloxy]-1,1-dimethyl-1-silaethane

Conditions

Conditions	Yield
With triethylamine; sodium iodide In acetonitrile at 20℃; for 4h; Inert atmosphere;	99%

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

: carvomenthide

Conditions

Conditions	Yield
With 3-chloro-benzenecarboperoxoic acid In chloroform at 0℃; for 48h; Inert atmosphere;	65.4%

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

A: 54783-36-7
Ψ-diosphenol

B: (6S)-(+)-diosphenol

C: (6R)-(-)-diosphenol

Conditions

Conditions	Yield
Stage #1: (5S)-2-methyl-5-(methylethyl)cyclohexan-1-one With bromine In diethyl ether at -10℃; for 7h; Stage #2: With sodium hydroxide In tetrahydrofuran at -10℃; for 0.833333h;	A 12% B n/a C n/a

...Expand

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

: (5R)-2-chloro-2-methyl-5-isopropylcyclohexanone

Conditions

Conditions	Yield
With sulfuryl dichloride In tetrachloromethane

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

A: (5S)-2-chloro-2-methyl-5-isopropylcyclohexanone

B: (5S)-2-chloro-2-methyl-5-isopropylcyclohexanone

Conditions

Conditions	Yield
With sulfuryl dichloride In tetrachloromethane optical yield given as %de;

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

: 1309659-99-1
(2S,5S)-2-methyl-5-(methylethyl)-2-prop-2-enylcyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: triethylamine; sodium iodide / acetonitrile / 4 h / 20 °C / Inert atmosphere 2: tris-(dibenzylideneacetone)dipalladium(0); (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol; tetrabutylammonium triphenyldifluorosilicate / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere View Scheme

: 160168-89-8
(5S)-2-methyl-5-(methylethyl)cyclohexan-1-one

A: 1309659-99-1
(2S,5S)-2-methyl-5-(methylethyl)-2-prop-2-enylcyclohexan-1-one

B: 1309660-01-2
(2R,5S)-2-methyl-5-(methylethyl)-2-prop-2-enylcyclohexan-1-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1.1: triethylamine; sodium iodide / acetonitrile / 4 h / 20 °C / Inert atmosphere 2.1: methyllithium / tetrahydrofuran; 1,2-dimethoxyethane / 1 h / -40 °C / Inert atmosphere 2.2: 19 h / -50 °C / Inert atmosphere 2.3: Inert atmosphere View Scheme

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Hebei Nengqian Chemical Import and Export Co., LTD

Zibo Hangyu Biotechnology Development Co., Ltd

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Xi`an Eastling Biotech Co., Ltd.

Antimex Chemical Limied

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