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122-96-3

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122-96-3 Usage

Chemical Properties

white crystalline powder

Uses

1,4-Piperazinediethanol is useful in the synthesis of salt-inducible kinase inhibitors for the treatment of diseases.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 122-96-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122-96:
(5*1)+(4*2)+(3*2)+(2*9)+(1*6)=43
43 % 10 = 3
So 122-96-3 is a valid CAS Registry Number.

122-96-3 Well-known Company Product Price

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

  • (H55063)  1,4-Bis(2-hydroxyethyl)piperazine, 98%   

  • 122-96-3

  • 5g

  • 415.0CNY

  • Detail
  • Alfa Aesar

  • (H55063)  1,4-Bis(2-hydroxyethyl)piperazine, 98%   

  • 122-96-3

  • 25g

  • 1430.0CNY

  • Detail
  • Aldrich

  • (B45402)  1,4-Bis(2-hydroxyethyl)piperazine  99%

  • 122-96-3

  • B45402-5G

  • 448.11CNY

  • Detail
  • Aldrich

  • (B45402)  1,4-Bis(2-hydroxyethyl)piperazine  99%

  • 122-96-3

  • B45402-25G

  • 1,539.72CNY

  • Detail

122-96-3SDS

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 1,4-Bis(2-hydroxyethyl)piperazine

1.2 Other means of identification

Product number -
Other names 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Solvents (which become part of product formulation or mixture)
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:122-96-3 SDS

122-96-3Synthetic route

piperazine
110-85-0

piperazine

2-bromoethanol
540-51-2

2-bromoethanol

A

1-(2-hydroxyethyl)piperazine
103-76-4

1-(2-hydroxyethyl)piperazine

B

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With hydrogenchloride In methanol; water for 2.5h; pH=8.5; pH-value; Reagent/catalyst; Inert atmosphere;A 86.2%
B n/a
2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With hydrogen at 180 - 200℃; under 60006 Torr; for 10h; Product distribution / selectivity; Autoclave; Inert atmosphere;79%
With water at 150℃; under 26478.3 Torr; Anfangsdruck, unter CO2;
With phosphoric acid at 250℃; unter CO2;
1-(2-hydroxyethyl)piperazine
103-76-4

1-(2-hydroxyethyl)piperazine

2-bromoethanol
540-51-2

2-bromoethanol

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In acetonitrile for 18h; Reflux; Inert atmosphere;45%
ethanolamine
141-43-5

ethanolamine

A

1-(2-hydroxyethyl)piperazine
103-76-4

1-(2-hydroxyethyl)piperazine

B

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium hydrogencarbonate In water at 140℃; for 96h; Inert atmosphere; Heating;A 30%
B 27%
oxirane
75-21-8

oxirane

piperazine
110-85-0

piperazine

A

1-(2-hydroxyethyl)piperazine
103-76-4

1-(2-hydroxyethyl)piperazine

B

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With methanol
With methanol
oxirane
75-21-8

oxirane

piperazine
110-85-0

piperazine

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With methanol
Yield given;
piperazine
110-85-0

piperazine

2-chloro-ethanol
107-07-3

2-chloro-ethanol

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
at 105℃;
With ethanol
phenylacetonitrile
140-29-4

phenylacetonitrile

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
auf Siedetemperatur;
ethanolamine
141-43-5

ethanolamine

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With sodium carbonate; ethylene dibromide
ethylenediamine
107-15-3

ethylenediamine

2-chloro-ethanol
107-07-3

2-chloro-ethanol

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With water
2-Spirocyclohexyl-3-(β-hydroxyethyl)oxazolidine
2359-11-7

2-Spirocyclohexyl-3-(β-hydroxyethyl)oxazolidine

A

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

B

cyclohexanone
108-94-1

cyclohexanone

Conditions
ConditionsYield
With PPA at 200℃; for 10h; Product distribution;
oxirane
75-21-8

oxirane

ammonium hydroxide

ammonium hydroxide

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

1,4-dioxane
123-91-1

1,4-dioxane

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

hydrogen

hydrogen

copper chromite

copper chromite

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
at 250 - 275℃; unter Druck;
benzonitrile
100-47-0

benzonitrile

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

A

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

B

ammonia
7664-41-7

ammonia

C

benzoic acid
65-85-0

benzoic acid

Conditions
ConditionsYield
die Umsetzung mit Benzylcyanid verlaeuft analog;
N,N'-tetra-(2-hydroxyethyl)oxamide

N,N'-tetra-(2-hydroxyethyl)oxamide

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
In acetone
N,N-tetra-(2-hydroxyethyl)oxamide

N,N-tetra-(2-hydroxyethyl)oxamide

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
In acetone
oxirane
75-21-8

oxirane

piperazine
110-85-0

piperazine

A

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

B

C10H22N2O3

C10H22N2O3

C

C12H26N2O4

C12H26N2O4

Conditions
ConditionsYield
With disodium hydrogenphosphate In water at 120℃; Large scale;
N-(2'-hydroxyethyl)-2-oxazolidone
3356-88-5

N-(2'-hydroxyethyl)-2-oxazolidone

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

Conditions
ConditionsYield
With ytterbium(III) triflate at 180℃; for 25h; Reagent/catalyst;
carbon dioxide
124-38-9

carbon dioxide

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

A

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

B

N-(2'-hydroxyethyl)-2-oxazolidone
3356-88-5

N-(2'-hydroxyethyl)-2-oxazolidone

Conditions
ConditionsYield
With alumina In ethanol at 250℃; under 112511 Torr; Catalytic behavior; Concentration; Temperature; Pressure; High pressure; Flow reactor; Supercritical conditions;
ethanol
64-17-5

ethanol

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

A

1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

B

C10H22N2O2

C10H22N2O2

Conditions
ConditionsYield
With alumina at 250℃; under 75007.5 Torr; High pressure; Flow reactor; Supercritical conditions;
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

potassium chloride

potassium chloride

palladium dichloride

palladium dichloride

[Pd(1,4-bis(2-hydroxyethyl)piperazine)Cl2]

[Pd(1,4-bis(2-hydroxyethyl)piperazine)Cl2]

Conditions
ConditionsYield
In water at 70℃;92%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

2-Thiophenecarbonyl chloride
5271-67-0

2-Thiophenecarbonyl chloride

C18H22N2O4S2
80838-52-4

C18H22N2O4S2

Conditions
ConditionsYield
In benzene for 1h; Heating;91%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

1,4-bis(2-chloroethyl)piperazine dihydrochloride
1428-92-8, 63980-44-9, 93335-18-3

1,4-bis(2-chloroethyl)piperazine dihydrochloride

Conditions
ConditionsYield
With thionyl chloride In chloroform; N,N-dimethyl-formamide for 6.5h; Heating;88%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

2-furancarbonyl chloride
527-69-5

2-furancarbonyl chloride

C18H22N2O6
80838-46-6

C18H22N2O6

Conditions
ConditionsYield
In benzene for 1h; Heating;87%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

butyric acid
107-92-6

butyric acid

Buttersaeure-N,N'-bis--piperazindiester

Buttersaeure-N,N'-bis--piperazindiester

Conditions
ConditionsYield
Stage #1: butyric acid With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 0.283333h;
Stage #2: 1,4-bis(2-hydroxyethyl)piperazine In dichloromethane at 20℃;
87%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

sodium saccharinate dihydrate
6155-57-3

sodium saccharinate dihydrate

silver nitrate

silver nitrate

[Ag(μ-saccharinato)(μ-N,N'-bis(2-hydroxyethyl)piperazine)](n)

[Ag(μ-saccharinato)(μ-N,N'-bis(2-hydroxyethyl)piperazine)](n)

Conditions
ConditionsYield
In water; isopropyl alcohol Na salt added to a soln. of AgNO3 in H2O and isopropanol, an aq. soln. of HOC2H4N(C2H4)2NC2H4OH added dropwise; crystd. for 4 d in the dark at room temp.; elem. anal.;86%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

acetic anhydride
108-24-7

acetic anhydride

1,4-bis-(2-acetoxy-ethyl)-piperazine
20727-34-8

1,4-bis-(2-acetoxy-ethyl)-piperazine

Conditions
ConditionsYield
With sulfuric acid Cooling with ice;85%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

N,N'-bis(2-bromoethyl)piperazine dihydrobromide
90942-23-7

N,N'-bis(2-bromoethyl)piperazine dihydrobromide

Conditions
ConditionsYield
With hydrogen bromide for 24h; Reflux; Inert atmosphere;84%
With water; hydrogen bromide
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

diphenylborinic acid
2622-89-1

diphenylborinic acid

(N->B),(N->B)'-bisdiphenyl-[2,2'-(1,4-piperazinediethoxy)]bisborane
207730-12-9

(N->B),(N->B)'-bisdiphenyl-[2,2'-(1,4-piperazinediethoxy)]bisborane

Conditions
ConditionsYield
In methanol addn. of 2 equiv. of B-compd. to piperazine derivative soln. at -78°C (pptn.); filtration (under N2), washing (hexane), drying;78%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

2-(2,4,5-trichlorophenoxy)acetyl chloride
777-08-2

2-(2,4,5-trichlorophenoxy)acetyl chloride

1,4-bis<2-(2,4,5-trichlorophenoxyacetoxy)ethyl>piperazine dihydrochloride
105115-40-0

1,4-bis<2-(2,4,5-trichlorophenoxyacetoxy)ethyl>piperazine dihydrochloride

Conditions
ConditionsYield
In N,N-dimethyl-formamide 1.) 60 deg C, 2.) 100 deg C, 5 h.;71%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

benzene-1,3,5-tricarboxylic acid
554-95-0

benzene-1,3,5-tricarboxylic acid

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

zinc(II) chloride
7646-85-7

zinc(II) chloride

(NH2Me2)(1,4-bis(2-hydroxyethyl)piperazine-H2)[Zn3(trimesate)3]·3H2O

(NH2Me2)(1,4-bis(2-hydroxyethyl)piperazine-H2)[Zn3(trimesate)3]·3H2O

Conditions
ConditionsYield
at 100℃; for 24h;65%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

2-mercapto-3H-quinazolin-4-one
13906-09-7

2-mercapto-3H-quinazolin-4-one

2,2'-((piperazine-1,4-diylbis(ethane-2,1-diyl))bis(sulfanediyl))bis(quinazolin-4(3H)-one)

2,2'-((piperazine-1,4-diylbis(ethane-2,1-diyl))bis(sulfanediyl))bis(quinazolin-4(3H)-one)

Conditions
ConditionsYield
Stage #1: 1,4-bis(2-hydroxyethyl)piperazine; 2-mercapto-3H-quinazolin-4-one In N,N-dimethyl-formamide at 0℃; for 0.0833333h; Mitsunobu Displacement; Microwave irradiation; Inert atmosphere;
Stage #2: With di-isopropyl azodicarboxylate; trimethylphosphane In N,N-dimethyl-formamide; toluene at 0 - 40℃; for 0.5h; Mitsunobu Displacement; Microwave irradiation; Inert atmosphere;
63%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

chlorure de dimethyl-5,8 dioxa-2,11 aza-5 azonia-8 phospha-1 bicyclo 6.3.0 undecane
64762-33-0, 113986-23-5

chlorure de dimethyl-5,8 dioxa-2,11 aza-5 azonia-8 phospha-1 bicyclo 6.3.0 undecane

1,4-di(6,9-dimethyl-1,3-dioxa-6,9-diaza-2-phosphacycloundecan-2-yl)oxyethylpiperazine

1,4-di(6,9-dimethyl-1,3-dioxa-6,9-diaza-2-phosphacycloundecan-2-yl)oxyethylpiperazine

Conditions
ConditionsYield
With triethylamine In chloroform for 2h; Ambient temperature;62%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

naproxen
23981-80-8

naproxen

N,N'-di<α-(6-metossi-2-naftil)propionilossi-2-etil>piperazina

N,N'-di<α-(6-metossi-2-naftil)propionilossi-2-etil>piperazina

Conditions
ConditionsYield
With pyridine; dicyclohexyl-carbodiimide In tetrahydrofuran -20 deg C, 10 min; 0 deg C, 24 h; RT, 24 h;49%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

sodium tungstate (VI) dihydrate
10213-10-2

sodium tungstate (VI) dihydrate

nickel(II) nitrate hexahydrate

nickel(II) nitrate hexahydrate

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

Na2[Ni(N,N'-bis(2-hydroxyethyl)piperazinium)(water)4][PW10Ni2O38(N,N'-bis(2-hydroxyethyl)piperazinium)2]*8(water)

Na2[Ni(N,N'-bis(2-hydroxyethyl)piperazinium)(water)4][PW10Ni2O38(N,N'-bis(2-hydroxyethyl)piperazinium)2]*8(water)

Conditions
ConditionsYield
With HNO3; NaCl In water Na2WO4*2H2O dissolving in 1 M NaCl, addn. of 4 M HNO3 to pH 3.5, addn. of HOCH2CH2N(CH2CH2)2NCH2CH2OH and 85% H3PO4, addn. of 4 M HNO3 to pH 6.3, addn. of Ni(NO3)2*6H2O, heating to 50°C for 15 min; centrifugation, crystn. by slow evapn. at pH 6.1, isolation of crystals over the course of a week, elem. anal.;46.89%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

(6-(benzyloxy)-2-(4-(benzyloxy)phenyl)benzo[b]thiophen-3-yl)(4-fluorophenyl)methanone

(6-(benzyloxy)-2-(4-(benzyloxy)phenyl)benzo[b]thiophen-3-yl)(4-fluorophenyl)methanone

(6-(benzyloxy)-2-(4-(benzyloxy)phenyl)benzo[b]thiophen-3-yl)(4-(2-(4-(2-hydroxyethyl)piperazin-1-yl)ethoxy)phenyl)methanone

(6-(benzyloxy)-2-(4-(benzyloxy)phenyl)benzo[b]thiophen-3-yl)(4-(2-(4-(2-hydroxyethyl)piperazin-1-yl)ethoxy)phenyl)methanone

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 50℃; Inert atmosphere;46%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

butyric acid
107-92-6

butyric acid

C12H24N2O3

C12H24N2O3

Conditions
ConditionsYield
Stage #1: butyric acid With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 0.283333h;
Stage #2: 1,4-bis(2-hydroxyethyl)piperazine In dichloromethane at 20℃;
45%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

2,4,6-trimethylphenoxyacetyl chloride
20509-83-5

2,4,6-trimethylphenoxyacetyl chloride

(2,4,6-Trimethyl-phenoxy)-acetic acid 2-(4-{2-[2-(2,4,6-trimethyl-phenoxy)-acetoxy]-ethyl}-piperazin-1-yl)-ethyl ester; hydrochloride
86746-11-4

(2,4,6-Trimethyl-phenoxy)-acetic acid 2-(4-{2-[2-(2,4,6-trimethyl-phenoxy)-acetoxy]-ethyl}-piperazin-1-yl)-ethyl ester; hydrochloride

Conditions
ConditionsYield
In N,N-dimethyl-formamide 1.) 60 deg C, 2.) 100 deg C, 5 h.;43%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

maleic acid monomethyl ester
44836-34-2

maleic acid monomethyl ester

(E)-but-2-enedioic acid-2-{4-[2-((E)-3-methoxycarbonyl-acryloyloxy)-ethyl]-piperazin-1-yl}-ethyl ester methyl ester dihydrochloride

(E)-but-2-enedioic acid-2-{4-[2-((E)-3-methoxycarbonyl-acryloyloxy)-ethyl]-piperazin-1-yl}-ethyl ester methyl ester dihydrochloride

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 23℃; for 14h;42%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

maleic acid monomethyl ester
44836-34-2

maleic acid monomethyl ester

(E)-but-2-enedioic acid-2-{4-[2-((E)-3-methoxycarbonyl-acryloyloxy)-ethyl]-piperazin-1-yl}-ethyl ester methyl ester

(E)-but-2-enedioic acid-2-{4-[2-((E)-3-methoxycarbonyl-acryloyloxy)-ethyl]-piperazin-1-yl}-ethyl ester methyl ester

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 23℃; for 14h;42%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

sodium tungstate (VI) dihydrate
10213-10-2

sodium tungstate (VI) dihydrate

manganese(II) nitrate

manganese(II) nitrate

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

sodium chloride
7647-14-5

sodium chloride

4Na(1+)*3C4H8N2H2(C2H4OH)2(2+)*P2Mn4W18O68(10-)*15H2O=Na4(C4H8N2H2(C2H4OH)2)3[P2Mn4W18O68]*15H2O

4Na(1+)*3C4H8N2H2(C2H4OH)2(2+)*P2Mn4W18O68(10-)*15H2O=Na4(C4H8N2H2(C2H4OH)2)3[P2Mn4W18O68]*15H2O

Conditions
ConditionsYield
With NaOH; nitric acid In water W compd. dissolved in aq. NaCl, acidified to pH 7.5 (nitric acid), amineadded, phosphoric acid added, pH adjusted to 6.8 (NaOH), aq. Mn compd. added; ppt. centrifuged, soln. heated to 60°C for 15 min, crysts. filtered; elem. anal.;39%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

4,4'-dimethoxytrityl chloride
40615-36-9

4,4'-dimethoxytrityl chloride

2-(4-{2-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-ethyl}-piperazin-1-yl)-ethanol

2-(4-{2-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-ethyl}-piperazin-1-yl)-ethanol

Conditions
ConditionsYield
With dmap; triethylamine In pyridine Ambient temperature;37%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

sodium tungstate (VI) dihydrate
10213-10-2

sodium tungstate (VI) dihydrate

manganese(II) nitrate

manganese(II) nitrate

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

sodium chloride
7647-14-5

sodium chloride

2Na(1+)*C4H8N2H(C2H4OH)2(1+)*5C4H8N2H2(C2H4OH)2(2+)*PO4(PMnW11O39)2(13-)*18H2O=Na2(C4H8N2(C2H4OH)2)6H11P3Mn2W22O82*18H2O

2Na(1+)*C4H8N2H(C2H4OH)2(1+)*5C4H8N2H2(C2H4OH)2(2+)*PO4(PMnW11O39)2(13-)*18H2O=Na2(C4H8N2(C2H4OH)2)6H11P3Mn2W22O82*18H2O

Conditions
ConditionsYield
With NaOH; nitric acid In water W compd. dissolved in aq. NaCl, acidified to pH 3.5 (nitric acid), amineadded, phosphoric acid added, pH adjusted to 6.05 (NaOH), aq. Mn compd. added; ppt. centrifuged, soln. stored for 3 wk., crysts. filtered; elem. anal.,TGA;25%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

acetic anhydride
108-24-7

acetic anhydride

C10H20N2O3

C10H20N2O3

Conditions
ConditionsYield
With sulfuric acid Cooling with ice;23%
1,4-bis(2-hydroxyethyl)piperazine
122-96-3

1,4-bis(2-hydroxyethyl)piperazine

1-(chloro(4-methoxyphenyl)(phenyl)methyl)-3-methoxybenzene

1-(chloro(4-methoxyphenyl)(phenyl)methyl)-3-methoxybenzene

C29H36O4N2

C29H36O4N2

Conditions
ConditionsYield
With dmap; triethylamine In pyridine at 20℃;13%

122-96-3Relevant articles and documents

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Bain,Pollard

, p. 532 (1939)

-

-

Adelson et al.

, p. 1988 (1935)

-

Continuous N-alkylation reactions of amino alcohols using γ-Al2O3 and supercritical CO2: Unexpected formation of cyclic ureas and urethanes by reaction with CO2

Streng, Emilia S.,Lee, Darren S.,George, Michael W.,Poliakoff, Martyn

, p. 329 - 337 (2017/03/15)

The use of γ-Al2O3 as a heterogeneous catalyst in scCO2 has been successfully applied to the amination of alcohols for the synthesis of N-alkylated heterocycles. The optimal reaction conditions (temperature and substrate flow rate) were determined using an automated self-optimising reactor, resulting in moderate to high yields of the target products. Carrying out the reaction in scCO2 was shown to be beneficial, as higher yields were obtained in the presence of CO2 than in its absence. A surprising discovery is that, in addition to cyclic amines, cyclic ureas and urethanes could be synthesised by incorporation of CO2 from the supercritical solvent into the product.

PREPARATION OF DIHYDROXYETHYL PIPERAZINE

-

Paragraph 32, (2014/03/26)

A process for selectively preparing dihydroxyethyl piperazine by reacting hydroxyethyloxazolidinone with an acid catalyst wherein the selectivity of hydroxyethyloxazolidinone to dihydroxyethyl piperazine is at least 55%.

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