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2008-75-5 Usage

Chemical Properties

Colorless to beige crystals

Uses

Different sources of media describe the Uses of 2008-75-5 differently. You can refer to the following data:
1. 1-(2-Chloroethyl)piperidine hydrochloride is used as intermediate for the syntheses of pharmaceuticals (e.g. fenpiverinium bromide, cloperastine and pitofenone).
2. Hydrochloride salt of N-(β-Chloroethyl)piperidine is used in the inhibition of sickle-cell hemoglobin.

Check Digit Verification of cas no

The CAS Registry Mumber 2008-75-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2008-75:
(6*2)+(5*0)+(4*0)+(3*8)+(2*7)+(1*5)=55
55 % 10 = 5
So 2008-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H14ClN/c8-4-7-9-5-2-1-3-6-9/h1-7H2/p+1

2008-75-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B22985)  1-(2-Chloroethyl)piperidine hydrochloride, 98%   

  • 2008-75-5

  • 50g

  • 253.0CNY

  • Detail
  • Alfa Aesar

  • (B22985)  1-(2-Chloroethyl)piperidine hydrochloride, 98%   

  • 2008-75-5

  • 250g

  • 1072.0CNY

  • Detail
  • Alfa Aesar

  • (B22985)  1-(2-Chloroethyl)piperidine hydrochloride, 98%   

  • 2008-75-5

  • 500g

  • 1463.0CNY

  • Detail
  • Aldrich

  • (C42602)  1-(2-Chloroethyl)piperidinehydrochloride  98%

  • 2008-75-5

  • C42602-100G

  • 545.22CNY

  • Detail
  • Aldrich

  • (C42602)  1-(2-Chloroethyl)piperidinehydrochloride  98%

  • 2008-75-5

  • C42602-500G

  • 2,005.38CNY

  • Detail

2008-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroethyl)piperidine,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(2-Chloroethyl)piperidine Hydrochloride

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:2008-75-5 SDS

2008-75-5Synthetic route

1-piperidinoethanol
3040-44-6

1-piperidinoethanol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

Conditions
ConditionsYield
With thionyl chloride In chloroform for 3h; Cooling with ice; Reflux;85%
With hydrogenchloride; thionyl chloride In chloroform for 1h; Heating / reflux;76%
With thionyl chloride In chloroform for 4h; Reflux; Cooling with ice;
piperidine
110-89-4

piperidine

2-chloro-ethanol
107-07-3

2-chloro-ethanol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

Conditions
ConditionsYield
Stage #1: piperidine; 2-chloro-ethanol In toluene for 3h; Reflux;
Stage #2: With thionyl chloride In toluene for 2h; Reflux;
59.2%
Stage #1: piperidine; 2-chloro-ethanol In toluene for 2h; Reflux;
Stage #2: With thionyl chloride In toluene at 20℃; for 8h; Cooling with ice;
15.5 g
trans-4-bromo-N-methyl-N-[4-(2-piperidin-1-yl-ethoxy)-cyclohexyl]-benzenesulfonamide

trans-4-bromo-N-methyl-N-[4-(2-piperidin-1-yl-ethoxy)-cyclohexyl]-benzenesulfonamide

A

trans-4-Bromo-N-(4-hydroxy-cyclohexyl)-N-methyl-benzenesulfonamide

trans-4-Bromo-N-(4-hydroxy-cyclohexyl)-N-methyl-benzenesulfonamide

B

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

trans-N-Methyl-N-[4-(2-piperidin-1-yl-ethoxy)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide

trans-N-Methyl-N-[4-(2-piperidin-1-yl-ethoxy)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide

A

trans-N-(4-hydroxy-cyclohexyl)-N-methyl-4-trifluoro-methyl-benzenesulfonamide

trans-N-(4-hydroxy-cyclohexyl)-N-methyl-4-trifluoro-methyl-benzenesulfonamide

B

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

4-[6-methoxy-2-(3-methoxyphenyl)-1-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl]phenol
573674-55-2

4-[6-methoxy-2-(3-methoxyphenyl)-1-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl]phenol

6-methoxy-2-(3-methoxyphenyl)-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinoline
573674-57-4

6-methoxy-2-(3-methoxyphenyl)-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinoline

Conditions
ConditionsYield
Stage #1: 4-[6-methoxy-2-(3-methoxyphenyl)-1-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl]phenol With sodium hydride In 1,4-dioxane at 20℃; for 0.166667h;
Stage #2: N-chloroethylpiperidine hydrochloride With sodium hydride In 1,4-dioxane at 80℃; for 5h;
100%
4-bromo-phenol
106-41-2

4-bromo-phenol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-[2-(4-bromophenoxy)ethyl]piperidine
836-58-8

1-[2-(4-bromophenoxy)ethyl]piperidine

Conditions
ConditionsYield
With caesium carbonate; potassium iodide In N,N-dimethyl-formamide at 25 - 50℃; for 14.5h;100%
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane; water at 20 - 35℃; for 18h;98.5%
With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In dichloromethane at 30 - 35℃; for 18h; Industrial scale;98.2%
5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-ol
710348-61-1

5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-ol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-[2-(5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yloxy)ethyl]piperidine
710348-59-7

1-[2-(5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yloxy)ethyl]piperidine

Conditions
ConditionsYield
With sodium hydride In DMF (N,N-dimethyl-formamide) at 20℃;100%
[6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl](4-hydroxyphenyl)methanone
63676-19-7

[6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl](4-hydroxyphenyl)methanone

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

[6-Methoxy-2-(4-Methoxyphenyl)benzo[b]thien-3-yl]-[4-[2-(1-Piperidinyl)ethoxy]phenyl] Methanone
84541-38-8

[6-Methoxy-2-(4-Methoxyphenyl)benzo[b]thien-3-yl]-[4-[2-(1-Piperidinyl)ethoxy]phenyl] Methanone

Conditions
ConditionsYield
In dichloromethane; water at 16 - 20℃; for 6.5h; Product distribution / selectivity; Reflux;100%
With sodium hydroxide In dichloromethane; water at 16 - 20℃; for 6.75h; Product distribution / selectivity; Reflux;100%
With sodium hydroxide In dichloromethane; water at 16℃; for 6.5h; Product distribution / selectivity; Reflux;100%
4-(Diethylamino)salicylaldehyde
17754-90-4

4-(Diethylamino)salicylaldehyde

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

4-diethylamino-2-[2-(1-piperidyl)ethoxy]benzaldehyde
1402729-63-8

4-diethylamino-2-[2-(1-piperidyl)ethoxy]benzaldehyde

Conditions
ConditionsYield
With caesium carbonate In acetonitrile at 80℃; for 4h;100%
1-(4-Hydroxyphenyl)-2-phenylethanone
2491-32-9

1-(4-Hydroxyphenyl)-2-phenylethanone

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

2-phenyl(4-piperidinylethoxyphenyl)ethan-1-one

2-phenyl(4-piperidinylethoxyphenyl)ethan-1-one

Conditions
ConditionsYield
With potassium carbonate In acetone for 6h; Heating;99%
5-nitroguaiacol
636-93-1

5-nitroguaiacol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-[2-(2-methoxy-5-nitro-phenoxy)-ethyl]-piperidine
399579-80-7

1-[2-(2-methoxy-5-nitro-phenoxy)-ethyl]-piperidine

Conditions
ConditionsYield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 72h;99%
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 72h;99%
With potassium carbonate In 1,2-dimethoxyethane at 20℃; for 24h;
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h;
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-(2-{4-[2-(3-fluoro-phenyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine
861930-34-9

1-(2-{4-[2-(3-fluoro-phenyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Conditions
ConditionsYield
Stage #1: 4-[2-(3-fluoro-phenyl)-6-methoxy-naphthalen-1-yloxy]-phenol With sodium hydride In DMF (N,N-dimethyl-formamide) at 20℃; for 0.5h;
Stage #2: N-chloroethylpiperidine hydrochloride for 72h;
99%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-(2-{4-[6-benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

1-(2-{4-[6-benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Conditions
ConditionsYield
Stage #1: 4-[6-benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-phenol With sodium hydride In DMF (N,N-dimethyl-formamide) at 20℃; for 0.5h;
Stage #2: N-chloroethylpiperidine hydrochloride
99%
6-bromobenzo[d]oxazol-2(3H)-one
19932-85-5

6-bromobenzo[d]oxazol-2(3H)-one

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

6-bromo-3-[2-(piperidin-1-yl)ethyl]-1,3-benzoxazol-2-one

6-bromo-3-[2-(piperidin-1-yl)ethyl]-1,3-benzoxazol-2-one

Conditions
ConditionsYield
Stage #1: 6-bromobenzo[d]oxazol-2(3H)-one With potassium carbonate In acetonitrile at 80℃; for 0.5h;
Stage #2: N-chloroethylpiperidine hydrochloride In acetonitrile at 80℃; for 12h;
99%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

2-((3-(2-(piperidin-1-yl)ethoxy)phenyl)amino)-9-cyclopentyl-8-((2-fluorophenyl)amino)-9H-purine

2-((3-(2-(piperidin-1-yl)ethoxy)phenyl)amino)-9-cyclopentyl-8-((2-fluorophenyl)amino)-9H-purine

Conditions
ConditionsYield
With sodium hydroxide In tetrahydrofuran; water at 55℃;98%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

17α-ethynyl-3E-oximino-4-androsten-17β-ol
54081-76-4

17α-ethynyl-3E-oximino-4-androsten-17β-ol

17α-ethynyl-3E-[O-(2-piperidinoethyl)]oximino-4-androsten-17β-ol

17α-ethynyl-3E-[O-(2-piperidinoethyl)]oximino-4-androsten-17β-ol

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In butanone for 48h; Heating;97.05%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

3-[3-chloro-4'-(2-piperidin-1-yl-ethoxy)-biphenyl-4-ylmethyl]-1-cyclohexyl-pyrrolidin-2-one hydrochloride

3-[3-chloro-4'-(2-piperidin-1-yl-ethoxy)-biphenyl-4-ylmethyl]-1-cyclohexyl-pyrrolidin-2-one hydrochloride

Conditions
ConditionsYield
Stage #1: 3-(3-chloro-4'-hydroxy-biphenyl-4-ylmethyl)-1-cyclohexyl-pyrrolidin-2-one With potassium carbonate; caesium carbonate In acetone at 20℃; for 0.0833333h;
Stage #2: N-chloroethylpiperidine hydrochloride In acetone at 50℃;
97%
(4-fluorophenyl)phenylmethanone oxime
362-99-2

(4-fluorophenyl)phenylmethanone oxime

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

(4-fluoro-phenyl)-phenyl-methanone O-(2-piperidin-1-yl-ethyl)-oxime

(4-fluoro-phenyl)-phenyl-methanone O-(2-piperidin-1-yl-ethyl)-oxime

Conditions
ConditionsYield
With sodium hydroxide; 18-crown-6 ether In dimethyl sulfoxide at 40℃; for 48h;96%
9a-butyl-4-(4-hydroxyphenyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
371757-03-8

9a-butyl-4-(4-hydroxyphenyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one

MeOH+1% Et3N

MeOH+1% Et3N

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one
371757-04-9

9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one

Conditions
ConditionsYield
With caesium carbonate In ethyl acetate; acetone96%
meta-nitrophenol
554-84-7

meta-nitrophenol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-(2-(3-nitrophenoxy)ethyl)piperidine
891855-93-9

1-(2-(3-nitrophenoxy)ethyl)piperidine

Conditions
ConditionsYield
Stage #1: meta-nitrophenol With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 0.0833333h;
Stage #2: N-chloroethylpiperidine hydrochloride In N,N-dimethyl-formamide at 80℃; for 0.25h;
96%
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 48h;54%
(E)-3-(3,4-bis(methoxymethoxy)phenyl)-1-(4-hydroxyphen-yl)prop-2-en-1-one

(E)-3-(3,4-bis(methoxymethoxy)phenyl)-1-(4-hydroxyphen-yl)prop-2-en-1-one

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

(E)-3-(3,4-bis(methoxymethoxy)phenyl)-1-(4-(2-(piperidin-1-yl)ethoxy)phenyl)prop-2-en-1-one

(E)-3-(3,4-bis(methoxymethoxy)phenyl)-1-(4-(2-(piperidin-1-yl)ethoxy)phenyl)prop-2-en-1-one

Conditions
ConditionsYield
With potassium carbonate In acetone at 60℃; for 8h;96%
tert-butyl 4-(4-hydroxy-2,6-difluoro-phenyl)-piperazine-1-carboxylate

tert-butyl 4-(4-hydroxy-2,6-difluoro-phenyl)-piperazine-1-carboxylate

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

tert-butyl 4-(2,6-difluoro-4-(2-(piperidin-1-yl)ethoxy)phenyl)piperazine-1-carboxylate

tert-butyl 4-(2,6-difluoro-4-(2-(piperidin-1-yl)ethoxy)phenyl)piperazine-1-carboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50 - 60℃; for 17h;96%
With potassium carbonate In N,N-dimethyl-formamide at 50 - 60℃; for 17h;96%
With potassium carbonate In N,N-dimethyl-formamide at 50 - 60℃; for 17h;390 mg
2-ethylthiophenol
4500-58-7

2-ethylthiophenol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1-[2-((2-ethylphenyl)thio)ethyl]piperidine

1-[2-((2-ethylphenyl)thio)ethyl]piperidine

Conditions
ConditionsYield
With sodium hydroxide In ethanol for 4h; Reflux;96%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

β-naphthol
135-19-3

β-naphthol

1-(2-(naphthalen-2-yloxy)ethyl)piperidine
1222-85-1

1-(2-(naphthalen-2-yloxy)ethyl)piperidine

Conditions
ConditionsYield
Stage #1: β-naphthol With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 0.166667h;
Stage #2: N-chloroethylpiperidine hydrochloride In N,N-dimethyl-formamide at 100℃; for 0.5h;
96%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

methyl 4-hydroxylbenzoate
99-76-3

methyl 4-hydroxylbenzoate

A

4-[2-(N-piperidine)-ethoxy]benzoic acid methyl ester
89407-97-6

4-[2-(N-piperidine)-ethoxy]benzoic acid methyl ester

B

4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride
84449-80-9

4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride

Conditions
ConditionsYield
With potassium carbonate In Isopropyl acetate; waterA n/a
B 95.3%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

(+/-)-cis-4-(4-hydroxyphenyl)-7-methoxy-3-(4-(trifluoromethyl)phenyl)chromane

(+/-)-cis-4-(4-hydroxyphenyl)-7-methoxy-3-(4-(trifluoromethyl)phenyl)chromane

(+/-)-cis-7-methoxy-4-(4-(2-piperidinoethoxy)phenyl)-3-(4-(trifluoromethyl)phenyl)chromane

(+/-)-cis-7-methoxy-4-(4-(2-piperidinoethoxy)phenyl)-3-(4-(trifluoromethyl)phenyl)chromane

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In acetone at 60℃; for 24h;95%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

3-(4-chlorophenyl)-2-mercaptothieno[2,3-d]pyrimidin-4(3H)-one
468096-21-1

3-(4-chlorophenyl)-2-mercaptothieno[2,3-d]pyrimidin-4(3H)-one

3-(4-chlorophenyl)-2-[(2-piperidin-1-ylethyl)thio]thieno[2,3-d]pyrimidin-4(3H)-one
468096-29-9

3-(4-chlorophenyl)-2-[(2-piperidin-1-ylethyl)thio]thieno[2,3-d]pyrimidin-4(3H)-one

Conditions
ConditionsYield
With sodium hydroxide In water at 50℃; for 0.5h;95%
2-[cyclohexyl(phenyl)methyl]-6-methoxy-1H-benzimidazole
897445-88-4

2-[cyclohexyl(phenyl)methyl]-6-methoxy-1H-benzimidazole

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

2-(cyclohexyl-phenyl-methyl)-6-methoxy-1-(2-piperidin-1-yl-ethyl)-1H-benzoimidazole

2-(cyclohexyl-phenyl-methyl)-6-methoxy-1-(2-piperidin-1-yl-ethyl)-1H-benzoimidazole

Conditions
ConditionsYield
With sodium hydride; potassium iodide In tetrahydrofuran for 6h; Heating;95%
2-nitro-5-hydroxybenzaldehyde
42454-06-8

2-nitro-5-hydroxybenzaldehyde

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

2-nitro-5-(2-piperidin-1-ylethoxy)benzaldehyde
485844-02-8

2-nitro-5-(2-piperidin-1-ylethoxy)benzaldehyde

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 4h;95%
With potassium carbonate In N,N-dimethyl-formamide at 45℃; for 16h;85%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

1,1-bis(4-hydroxyphenyl)-2-phenyl-1-butene
91221-46-4

1,1-bis(4-hydroxyphenyl)-2-phenyl-1-butene

1,1-bis-[4-[2-(piperidin-1-yl)ethoxy]phenyl]-2-phenyl-1-butene

1,1-bis-[4-[2-(piperidin-1-yl)ethoxy]phenyl]-2-phenyl-1-butene

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 50℃; for 0.5h;95%
(4-hydroxyphenyl)methanol
623-05-2

(4-hydroxyphenyl)methanol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

[4-[2-(1-piperidinyl)ethoxy]phenyl]methanol
223251-13-6

[4-[2-(1-piperidinyl)ethoxy]phenyl]methanol

Conditions
ConditionsYield
Stage #1: (4-hydroxyphenyl)methanol With sodium hydroxide In water for 0.333333h;
Stage #2: N-chloroethylpiperidine hydrochloride With tetrabutylammomium bromide In water; toluene Reflux;
95%
With potassium carbonate; caesium carbonate In acetonitrile at 90℃; for 24h;44%
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
269409-70-3

4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

(4-(2-(piperidin-1-yl)ethoxy)phenyl)boronic acid
710348-58-6

(4-(2-(piperidin-1-yl)ethoxy)phenyl)boronic acid

Conditions
ConditionsYield
Stage #1: N-chloroethylpiperidine hydrochloride; 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol With potassium carbonate; 18-crown-6 ether In acetonitrile at 180℃; for 0.166667h; Microwave irradiation;
Stage #2: With methanol
95%
7-methyl-2,6-dithioxo-1,2,3,6-tetrahydropurine
33403-02-0

7-methyl-2,6-dithioxo-1,2,3,6-tetrahydropurine

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

2,6-bis(2-piperidinylethylthio)-7-methylpurine
1411565-21-3

2,6-bis(2-piperidinylethylthio)-7-methylpurine

Conditions
ConditionsYield
Stage #1: 7-methyl-2,6-dithioxo-1,2,3,6-tetrahydropurine With sodium hydroxide In 1,4-dioxane at 20℃; for 1h;
Stage #2: N-chloroethylpiperidine hydrochloride In 1,4-dioxane for 2h; Reflux;
95%
4-Iodophenol
540-38-5

4-Iodophenol

N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

4-[2-(piperidin-1-yl)-ethoxy]-iodobenzene
103808-68-0

4-[2-(piperidin-1-yl)-ethoxy]-iodobenzene

Conditions
ConditionsYield
With potassium carbonate In acetone at 56℃; for 3h;95%
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 6h;77%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 50℃;

2008-75-5Relevant articles and documents

Coumadin female phenol split-ring analogue and its medical use

-

Paragraph 0042-0044, (2017/10/06)

The invention relates to the field of pharmaceutical chemistry, in particular to a coumestrol open-ring analogue with structures as shown in general formulae I and II and a medical application thereof, especially an application to the preparation of drugs as angiogenesis inhibition and vascular disruption agents.

Side chain impacts on pH- and thermo-responsiveness of tertiary amine functionalized polypeptides

Xiao, Chunsheng,Cheng, Yilong,Zhang, Yu,Ding, Jianxun,He, Chaoliang,Zhuang, Xiuli,Chen, Xuesi

, p. 671 - 679 (2014/02/14)

The systemic investigation of the structural impacts of side chains on the pH- and thermo-responsiveness of tertiary amine functionalized poly(l-glutamate)s (TA-PGs) was carried out. The TA-PGs polymers were effectively synthesized by Cu(I)-catalyzed azide-alkyne cycloaddition click reaction of azido tertiary amines with poly(γ-propargyl-l-glutamate) (PPLG). Turbimetric measurements were performed to characterize the pH- and temperature-induced phase transition of TA-PGs in aqueous solution, which suggested a structural dependence of the properties on the N-substituted groups and the "linkers" between 1,2,3-triazole ring and the tertiary amine groups in the side chains. In detail, the pH responsive properties of TA-PGs were basically determined by the hydrophobicity of the N-substituted groups in the side chains and the pH transition point (pHt) decreased as the increasing hydrophobicity of the N-substituted groups, while the temperature-responsiveness of TA-PGs were affected by either the N-substituted groups or the "linkers." TA-PGs with a moderate N-substituted amine group (e.g., DEA, PR, and PD) or a branched "linker" (e.g., iso-propylene and 2-methylpropylene group) were more likely to express the LCST-type phase transition tuned by pH variation. These structure-property relationships revealed in this study would help to develop the applications of TA-PGs in smart drug delivery systems. Copyright

Methods and compositions for treating amyloid-related diseases

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Page/Page column 160-161, (2010/11/24)

Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.

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