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1484-84-0

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1484-84-0 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 1484-84-0 differently. You can refer to the following data:
1. Reactant for syntehsis of: Spiroimidazolidinone NPC1L1 inhibitors P2Y12 antagonists for inhibition of platelet aggregation Cyclin-dependent kinase inhibitors Anti-HIV agents Tetraponerine analogsReactant for cyclization of secondary homoallylic amines
2. Heterocyclic compound used in cosmetic compositions.
3. 2-Piperidineethanol is useful in preparation of a novel class of pyrazolopyrimidines as inhibitors of protein and checkpoint kinases useful in treatment and prophylaxis of HCV infection and other diseases such as cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 1484-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1484-84:
(6*1)+(5*4)+(4*8)+(3*4)+(2*8)+(1*4)=90
90 % 10 = 0
So 1484-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO/c9-6-4-7-3-1-2-5-8-7/h7-9H,1-6H2/p+1/t7-/m0/s1

1484-84-0 Well-known Company Product Price

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  • Aldrich

  • (433594)  2-Piperidineethanol  technical grade, 90%

  • 1484-84-0

  • 433594-25G

  • 992.16CNY

  • Detail

1484-84-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Piperidineethanol

1.2 Other means of identification

Product number -
Other names 2PPRE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1484-84-0 SDS

1484-84-0Synthetic route

2-(2-Hydroxyethyl)pyridine
103-74-2

2-(2-Hydroxyethyl)pyridine

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
With 1,4-dioxane; nickel at 160℃; under 191232 Torr; Hydrogenation;
With ethanol; nickel at 150℃; under 95616 Torr; Hydrogenation;
With acetic acid; platinum Hydrogenation;
N-benzyl-2-(2-hydroxyethyl)piperidine
134256-32-9, 134256-31-8, 134256-33-0, 119204-13-6

N-benzyl-2-(2-hydroxyethyl)piperidine

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
With palladium on activated charcoal; ammonium formate In methanol for 12h; Heating; Yield given;
α-picolylcarbinol

α-picolylcarbinol

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
With ethanol; sodium
α-picolyl-carbinol

α-picolyl-carbinol

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
With ethanol; sodium
piperidine
110-89-4

piperidine

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 30 percent / H2O2, sodium tungstate dihydrate / methanol / under 5 deg C, then Rt, 24 h
2: CH2Cl2 / 12 h / Heating
3: 94 percent / LiAlH4 / tetrahydrofuran / 0 deg C, then reflux, 3 h
4: ammonium formate, 10percent Pd/C / methanol / 12 h / Heating
View Scheme
2-isobutoxyhexahydroisoxazolo<2,3-a>-pyridine
119204-12-5

2-isobutoxyhexahydroisoxazolo<2,3-a>-pyridine

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: CH2Cl2 / 12 h / Heating
2: 94 percent / LiAlH4 / tetrahydrofuran / 0 deg C, then reflux, 3 h
3: ammonium formate, 10percent Pd/C / methanol / 12 h / Heating
View Scheme
(2S,3aR)-8-Benzyl-2-isobutoxy-hexahydro-isoxazolo[2,3-a]pyridin-8-ium; bromide
119204-19-2

(2S,3aR)-8-Benzyl-2-isobutoxy-hexahydro-isoxazolo[2,3-a]pyridin-8-ium; bromide

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 94 percent / LiAlH4 / tetrahydrofuran / 0 deg C, then reflux, 3 h
2: ammonium formate, 10percent Pd/C / methanol / 12 h / Heating
View Scheme
phenyl chloroformate
1885-14-9

phenyl chloroformate

A

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

B

3-(dimethylamino)propyl 2-[2-(hydroxyethyl)]piperidinecarboxylate

3-(dimethylamino)propyl 2-[2-(hydroxyethyl)]piperidinecarboxylate

Conditions
ConditionsYield
pyridine
phenyl chloroformate
1885-14-9

phenyl chloroformate

A

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

B

3-chloropropyl 2-[2-(hydroxyethyl)]piperidinecarboxylate

3-chloropropyl 2-[2-(hydroxyethyl)]piperidinecarboxylate

2-(2-Hydroxyethyl)pyridine
103-74-2

2-(2-Hydroxyethyl)pyridine

ruthenium
7440-18-8

ruthenium

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate
118811-03-3

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 4h;100%
With triethylamine In dichloromethane at 20℃;99%
With sodium carbonate In dichloromethane; water at 20℃; for 24h; Inert atmosphere;98%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

4-methoxy-2,6-dimethylbenzenesulfonyl chloride
55661-08-0

4-methoxy-2,6-dimethylbenzenesulfonyl chloride

C16H25NO4S
1186241-09-7

C16H25NO4S

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;100%
With triethylamine In dichloromethane at 0 - 20℃;100%
With triethylamine In dichloromethane at 0 - 20℃;
With triethylamine In dichloromethane at 0℃; for 1h;
With triethylamine In dichloromethane at 0 - 20℃;
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

S-tert-butoxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine
41840-28-2

S-tert-butoxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate
118811-03-3

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

Conditions
ConditionsYield
In chloroform99.9%
In chloroform
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

benzyl chloroformate
501-53-1

benzyl chloroformate

2-(2-hydroxyethyl)-piperidine-1-carboxylic acid benzyl ester
39945-50-1

2-(2-hydroxyethyl)-piperidine-1-carboxylic acid benzyl ester

Conditions
ConditionsYield
With potassium carbonate In ethanol; water at 0 - 20℃; for 3.25h;99%
With sodium carbonate In dichloromethane for 1h; Ambient temperature;87%
Stage #1: 2(RS)-(2-hydroxyethyl)piperidine With sodium hydrogencarbonate In dichloromethane at 20℃;
Stage #2: benzyl chloroformate In dichloromethane at 0℃; for 1h;
63%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

hexahydro-3H-pyrido<1,2-c><1,3>oxazin-1-one
134415-15-9

hexahydro-3H-pyrido<1,2-c><1,3>oxazin-1-one

Conditions
ConditionsYield
With sodium methylate In methanol for 144h; Ambient temperature;98%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

2-<2-(tert-butyldimethylsiloxy)ethyl>piperidine
153108-62-4

2-<2-(tert-butyldimethylsiloxy)ethyl>piperidine

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 4h;98%
With 1H-imidazole In dichloromethane at 20℃; for 4.5h;98%
With 1H-imidazole In dichloromethane at 20℃; for 4h;90%
With 1H-imidazole In dichloromethane Inert atmosphere;78%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2-[1-(2-benzenesulfonyl-ethyl)-piperidin-2-yl]-ethanol
640297-00-3

2-[1-(2-benzenesulfonyl-ethyl)-piperidin-2-yl]-ethanol

Conditions
ConditionsYield
In xylene for 48h; Heating;95%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

5-benzoyl-3-(cyclopent-1-en-1-yl)-5-phenyl-1,5-dihydro-4H-pyrazol-4-one

5-benzoyl-3-(cyclopent-1-en-1-yl)-5-phenyl-1,5-dihydro-4H-pyrazol-4-one

N-benzoyl-2-(2-hydroxyethyl)piperidine
66120-20-5

N-benzoyl-2-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
In dichloromethane at 20℃; for 12h; regioselective reaction;95%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2-chloro-6-methoxy-3-nitropyridine
38533-61-8

2-chloro-6-methoxy-3-nitropyridine

2-(6'-methoxy-3'-nitro-3,4,5 6-tetrahydro-2H-[1,2']bipyridylyl-2-yl)ethanol

2-(6'-methoxy-3'-nitro-3,4,5 6-tetrahydro-2H-[1,2']bipyridylyl-2-yl)ethanol

Conditions
ConditionsYield
In ethanol for 2h; Heating / reflux;94.1%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

2-(3-nitrophenyl)-3-oxa-1-azabicyclo[4.4.0]decane

2-(3-nitrophenyl)-3-oxa-1-azabicyclo[4.4.0]decane

Conditions
ConditionsYield
94%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2-(2-Chloroethyl)piperidine Hydrochloride
60012-49-9

2-(2-Chloroethyl)piperidine Hydrochloride

Conditions
ConditionsYield
With thionyl chloride In chloroform for 2h; Heating;93%
With thionyl chloride In dichloromethane for 12h; Reflux;89%
With hydrogenchloride; chloroform Anschliessendes Erwaermen mit Thionylchlorid.;
With thionyl chloride In chloroform at 20℃; for 24h; Inert atmosphere; Cooling with ice;
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

n-valeryl chloride
638-29-9

n-valeryl chloride

1-pentanoyl-2-(2-hydroxyethyl)-piperidine

1-pentanoyl-2-(2-hydroxyethyl)-piperidine

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 18h; Acylation;93%
With sodium hydroxide; triethylamine In tetrahydrofuran; ethanol; dichloromethane
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

N-(Benzyloxycarbonyloxy)succinimide
13139-17-8

N-(Benzyloxycarbonyloxy)succinimide

2-(2-hydroxyethyl)-piperidine-1-carboxylic acid benzyl ester
39945-50-1

2-(2-hydroxyethyl)-piperidine-1-carboxylic acid benzyl ester

Conditions
ConditionsYield
In 1,4-dioxane; water at 25℃; for 24h;93%
With triethylamine In dichloromethane at 23℃; for 18h;43%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

3-bromo-2-isopropyl-5-methylthiophene-1,1-dioxide
167772-41-0

3-bromo-2-isopropyl-5-methylthiophene-1,1-dioxide

2-[1-((2E,4Z)-4-Bromo-6-methyl-hepta-2,4-dienyl)-piperidin-2-yl]-ethanol
203716-19-2

2-[1-((2E,4Z)-4-Bromo-6-methyl-hepta-2,4-dienyl)-piperidin-2-yl]-ethanol

Conditions
ConditionsYield
In xylene at 116℃; for 7.5h; Product distribution; other amines; amine-induced ring-opening reaction of 2-alkyl-3-bromo-5-methylthiophene-1,1-dioxides; optimization and mechanistic considerations; kinetic study; deuterium incorporation experiments; kinetic isotope effect;91%
In xylene at 116℃; for 7.5h;91%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

n-butyl isocyanide
111-36-4

n-butyl isocyanide

1-(Butylaminocarbonyl)-2-(2-hydroxyethyl)piperidine

1-(Butylaminocarbonyl)-2-(2-hydroxyethyl)piperidine

Conditions
ConditionsYield
In toluene at 20℃; for 1h; Addition;91%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

aniline
62-53-3

aniline

N-(2-piperidin-2-yl-ethyl)-aniline
26934-01-0

N-(2-piperidin-2-yl-ethyl)-aniline

Conditions
ConditionsYield
With cesiumhydroxide monohydrate; oxygen In 1,3,5-trimethyl-benzene at 180℃; for 24h;88%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

pivaloyl chloride
3282-30-2

pivaloyl chloride

2-(2-Hydroxyethyl)-1-(2,2-dimethylpropanoyl)piperidine
118671-56-0

2-(2-Hydroxyethyl)-1-(2,2-dimethylpropanoyl)piperidine

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 18h; Acylation;87%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

carbonochloridic acid, butyl ester
592-34-7

carbonochloridic acid, butyl ester

1-(Butoxycarbonyl)-2-(2-hydroxyethyl)-piperidine

1-(Butoxycarbonyl)-2-(2-hydroxyethyl)-piperidine

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 18h; Carboxylation;85%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

9-fluorenylmethyl N-succinimidyl carbonate
102774-86-7

9-fluorenylmethyl N-succinimidyl carbonate

2-(2-hydroxy-ethyl)-piperidine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester

2-(2-hydroxy-ethyl)-piperidine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 0.5h;85%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

Bis-(dimethylamino)-phenylboran
1201-45-2

Bis-(dimethylamino)-phenylboran

2-phenyl-1,3,2-oxazaborabicyclo[4.4.0]decane
66737-44-8

2-phenyl-1,3,2-oxazaborabicyclo[4.4.0]decane

Conditions
ConditionsYield
In benzene byproducts: MeNH2; absence of air; refluxing (5 h); solvent removal, distn.; elem. anal.;85%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

isopropyl chloroformate
108-23-6

isopropyl chloroformate

KBR 3023

KBR 3023

Conditions
ConditionsYield
With sodium hydroxide In toluene at 20℃; for 2h; Carboxylation;84%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

1,3-propanesultone
1120-71-4

1,3-propanesultone

3-[2-(2-hydroxyethyl)piperidin-1-yl]-1-propanesulfonic acid

3-[2-(2-hydroxyethyl)piperidin-1-yl]-1-propanesulfonic acid

Conditions
ConditionsYield
In tetrahydrofuran for 15h; Heating / reflux;84%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

4-((7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl)amino)benzonitrile

4-((7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl)amino)benzonitrile

4-((7-(3-(2-(2-hydroxyethyl)piperidin-1-yl)propoxy)-6-methoxyquinazolin-4-yl)amino)benzonitrile

4-((7-(3-(2-(2-hydroxyethyl)piperidin-1-yl)propoxy)-6-methoxyquinazolin-4-yl)amino)benzonitrile

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 60 - 80℃;84%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2-(piperidin-2-yl)acetic acid
19832-04-3

2-(piperidin-2-yl)acetic acid

Conditions
ConditionsYield
Stage #1: 2(RS)-(2-hydroxyethyl)piperidine With chromium(VI) oxide; sulfuric acid In water at 0 - 20℃; for 4.5h;
Stage #2: With barium dihydroxide In water
Stage #3: With carbon dioxide In water
83%
Stage #1: 2(RS)-(2-hydroxyethyl)piperidine With hydrogenchloride; sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium bromide In water; ethyl acetate at 5 - 20℃; for 0.833333h; pH=8.0 - 9.0;
Stage #2: With hydrogenchloride; sodium chlorite In water; ethyl acetate at 20 - 33℃; for 16.5h; pH=5.0;
78%
With chromium(VI) oxide; sulfuric acid at 0 - 20℃; for 15.25h; Jones oxidation;68%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2,6-dichlorobenzaldehyde
83-38-5

2,6-dichlorobenzaldehyde

α-(2,6-dichlorophenyl)-2-(2-hydroxyethyl)-1-piperidineacetonitrile
104062-11-5

α-(2,6-dichlorophenyl)-2-(2-hydroxyethyl)-1-piperidineacetonitrile

Conditions
ConditionsYield
With potassium cyanide In hydrogenchloride83%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

benzoyl chloride
98-88-4

benzoyl chloride

A

N-benzoyl-2-(2-hydroxyethyl)piperidine
66120-20-5

N-benzoyl-2-(2-hydroxyethyl)piperidine

B

Benzoic acid 2-(1-benzoyl-piperidin-2-yl)-ethyl ester

Benzoic acid 2-(1-benzoyl-piperidin-2-yl)-ethyl ester

Conditions
ConditionsYield
With di(n-butyl)tin oxide; triethylamine In toluene for 0.15h; Irradiation;A 82%
B 11%
With di(n-butyl)tin oxide; triethylamine In toluene for 0.15h; Irradiation;A 76%
B 19%
With triethylamine In tetrahydrofuran for 48h;
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate
118811-03-3

tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

Conditions
ConditionsYield
82%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

2-(2-bromoethyl)piperidine hydrobromide
1564-77-8

2-(2-bromoethyl)piperidine hydrobromide

Conditions
ConditionsYield
With hydrogen bromide In water for 24h; Reflux;82%
With hydrogen bromide In water Reflux;
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

N1-(2-chloro-9-isopropyl-9H-purin-6-yl)benzene-1,3-diamine

N1-(2-chloro-9-isopropyl-9H-purin-6-yl)benzene-1,3-diamine

2-(1-(6-((3-aminophenyl)amino)-9-isopropyl-9H-purin-2-yl)piperidin-2-yl)ethan-1-ol

2-(1-(6-((3-aminophenyl)amino)-9-isopropyl-9H-purin-2-yl)piperidin-2-yl)ethan-1-ol

Conditions
ConditionsYield
With potassium fluoride In 1-methyl-pyrrolidin-2-one Heating;81%
2(RS)-(2-hydroxyethyl)piperidine
1484-84-0

2(RS)-(2-hydroxyethyl)piperidine

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

1-(4-methoxyphenyl)octahydropyrido[1,2-c][1,3]oxazine

1-(4-methoxyphenyl)octahydropyrido[1,2-c][1,3]oxazine

Conditions
ConditionsYield
80%

1484-84-0Relevant articles and documents

Substituted Disulfonamide Compounds

-

Page/Page column 63, (2010/06/22)

Substituted disulfonamide compounds corresponding to formula I: In which R1, R2, R3, R4a, R4b, R5a, R5b, R8, R9a, R9b, R10, R11, a, b, s, t and A have defined meanings, pharmaceutical compositions containing one or more such compounds, processes for preparing such compounds, and a method of using such compounds for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin receptor 1 (BR1).

Process for the preparation of hydroxyethylcyclohexanes and hydroxyethylpiperidines

-

, (2008/06/13)

Hydroxyethylcyclohexanes which can optionally contain a nitrogen atom in the cyclohexane ring are obtained in a particularly selective manner by catalytic hydrogenation of the corresponding hydroxyethylbenzene or hydroxyethylpyridines when ruthenium which has been treated before use with a reducing agent is used as catalyst.

1,2-DI-substituted piperidine derivative, hair growth promoter and external composition for skin using the same

-

, (2008/06/13)

A 1,2-di-substituted piperidine derivative or a salt thereof expressed by the following Formula (I): wherein one of A and B is a hydrocarbon group of C1-30 expressed by R1 and the other is -(CH2)n-NR2R3; Y is -CO-, -CONR5- or -COO-; Z is -O-, -OCO-, -OCONR6- or -NR6-; R2 and R3 individually represent a hydrogen a lower alkyl, a phenyl or a benzyl group, or together represent a heterocycle having 3-7 members; -NR5-(CH2)n-NR2R3 and -NR6-(CH2)n-NR2R3 of -(Y)1-A and -Z-B may be the following Group W: wherein ring E is a heterocycle of 6 or 7 members including two nitrogen atoms and R2 is a hydrogen, a lower alkyl, a phenyl or a benzyl group; R4 is a hydrogen, a halogen, a lower alkyl, a lower acyl, a nitro, a cyano, a lower alkoxycarbonyl, a carbamoyl, a lower alkylcarbamoyl, a lower alkylamino, a lower acylamino, a lower alkoxy or a lower acyloxy group; each of R5 and R6 is a hydrogen, a lower alkyl, a lower acyl, a lower alkylcarbamoyl group, or a part of said ring E; l is 0 or 1; m is an integer of 2-5; and n is an integer of 0-5. The 1,2-di-substituted piperidine derivative or the salt thereof has excellent hair growth and regrowth promoting effects, which are useful for care, improvement or prevention of hair loss in mammals and, in particular, in human.

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