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Cas:105906-07-8
Min.Order:1 Gram
Negotiable
Type:Manufacturers
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Cas:105906-07-8
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
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Cas:105906-07-8
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
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Cas:105906-07-8
Min.Order:10 Gram
Negotiable
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Cas:105906-07-8
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:105906-07-8
Min.Order:0
Negotiable
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Trading Company
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Other
inquiryFINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 4-tert-Butylcyclohexyl acetic acid, CAS:105906-07-8 with the most competitive price a
Cas:105906-07-8
Min.Order:0
Negotiable
Type:Trading Company
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Cas:105906-07-8
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Cas:105906-07-8
Min.Order:0
Negotiable
Type:Trading Company
inquiry1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
With water; sodium hydroxide at 85℃; for 6h; | 85% |
(4-tert-Butylcyclohexyl)acetic acid methyl ester
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water for 3h; Heating; Yield given; | |
With sodium hydroxide In methanol |
(4-tert-Butyl-cyclohexyl)-cyano-acetic acid ethyl ester
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethylene glycol |
ethyl (4-t-butylcyclohexylidene)cyanoacetate
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaBH4 / ethanol / 1 h / 0 °C 2: KOH / ethane-1,2-diol View Scheme |
ethyl (4-tert-butylcyclohexylidene)acetate
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogen / palladium dichloride, activated carbon / methanol; aq. HCl 2: potassium hydroxide / ethanol; H2O / 3 h / Heating View Scheme |
4-tercbutyl-cyclohexanone
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium hydride / dimethylformamide / 1) 20 deg C, 1 h, 2) 90 deg C to 100 deg C, 8 h 2: hydrogen / palladium dichloride, activated carbon / methanol; aq. HCl 3: potassium hydroxide / ethanol; H2O / 3 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1.1: sodium hydride / mineral oil; tetrahydrofuran / 0.25 h / 0 °C 1.2: 2 h / 20 °C 2.1: hydrogen / methanol / 9 h / 55 °C / 7500.75 Torr 3.1: sodium hydroxide; water / 6 h / 85 °C View Scheme |
trans-4-tert-Butylcyclohexanecarbonitrile
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water |
diazomethane
1-trans-(4-t-butylcyclohexyl)-acetic acid
(4-tert-Butylcyclohexyl)acetic acid methyl ester
Conditions | Yield |
---|---|
94% |
diazomethane
1-trans-(4-t-butylcyclohexyl)-acetic acid
A
methyl trans-(4-t-butylcyclohexyl)acetate
B
methyl cis-(4-t-butylcyclohexyl)acetate
Conditions | Yield |
---|---|
Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
2-chloro-1,4-naphthoquinone
1-trans-(4-t-butylcyclohexyl)-acetic acid
2-(4-tert-Butyl-cyclohexylmethyl)-3-chloro-[1,4]naphthoquinone
Conditions | Yield |
---|---|
With ammonium persulfate; silver nitrate method of Jacobsen and Torssell; |
1-trans-(4-t-butylcyclohexyl)-acetic acid
(R)-4-(phenylmethyl)-2-oxazolidinone
Conditions | Yield |
---|---|
With n-butyllithium; pivaloyl chloride; triethylamine In tetrahydrofuran at -78 - 20℃; |
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: pivaloyl chloride, Et3N, n-BuLi / tetrahydrofuran / -78 - 20 °C 2: NaHMDS / tetrahydrofuran / -78 - 20 °C 3: nBuLi / tetrahydrofuran / -5 °C 4: TFA / CH2Cl2 / 4 °C View Scheme |
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: pivaloyl chloride, Et3N, n-BuLi / tetrahydrofuran / -78 - 20 °C 2: NaHMDS / tetrahydrofuran / -78 - 20 °C 3: nBuLi / tetrahydrofuran / -5 °C 4: TFA / CH2Cl2 / 4 °C 5: EDC, DMAP / CH2Cl2 / Ambient temperature View Scheme |
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: pivaloyl chloride, Et3N, n-BuLi / tetrahydrofuran / -78 - 20 °C 2: NaHMDS / tetrahydrofuran / -78 - 20 °C 3: nBuLi / tetrahydrofuran / -5 °C View Scheme |
1-trans-(4-t-butylcyclohexyl)-acetic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pivaloyl chloride, Et3N, n-BuLi / tetrahydrofuran / -78 - 20 °C 2: NaHMDS / tetrahydrofuran / -78 - 20 °C View Scheme |
1-trans-(4-t-butylcyclohexyl)-acetic acid
2-(trans-4-tert-butylcyclohexyl)methyl-3-hydroxynaphtho-1,4-quinone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: silver nitrate, ammonium persulphate / method of Jacobsen and Torssell 2: hydrolysis View Scheme |
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