Uses
ChemicalBook > CAS DataBase List > N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt

N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt

Uses
Product Name
N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt
CAS No.
208167-83-3
Chemical Name
N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt
Synonyms
tert-Butyl 4-(2-chloroethyl);1-Boc-4-(2-chloroethyl)piperazine;N-Boc-N'-(2-Chloroethyl)piperazine;1-Boc-4-(2-chloroethyl)piperazine,97%;1-Boc-4-(2-chloroethyl)piperazine, 97%;N-BOC-N''-(2-CHLOROETHYL)PIPERAZINE HYDROCHLORIDE;tert-Butyl 4-(2-chloroethyl)piperazine-1-carboxylate;N-BOC-Nzzhlxy-(2-Chloroethyl)piperazine hydrochloride;N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt;tert-Butyl 4-(2-chloroethyl)tetrahydropyrazine-1-carboxylate
CBNumber
CB21122356
Molecular Formula
C11H21ClN2O2
Formula Weight
248.75
MOL File
208167-83-3.mol
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N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt Property

Melting point:
67-69°C
Boiling point:
318.4±37.0 °C(Predicted)
Density 
1.106±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Slightly Soluble (7.2 g/L) (25°C).
form 
Crystalline Powder
pka
6.13±0.10(Predicted)
color 
White to light brown
InChI
InChI=1S/C11H21ClN2O2/c1-11(2,3)16-10(15)14-8-6-13(5-4-12)7-9-14/h4-9H2,1-3H3
InChIKey
MYOWELLYEZMECA-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)CCN(CCCl)CC1
CAS DataBase Reference
208167-83-3
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Safety

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933599590
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

TRC
Product number
B807083
Product name
tert-Butyl4-(2-Chloroethyl)piperazine-1-carboxylate
Packaging
50mg
Price
$60
Updated
2021/12/16
Matrix Scientific
Product number
046534
Product name
TERT-BUTYL 4-(2-CHLOROETHYL)PIPERAZINE-1-CARBOXYLATE
Purity
>95%
Packaging
1g
Price
$100
Updated
2021/12/16
Apolloscientific
Product number
OR15245
Product name
4-(2-Chloroethyl)piperazine,N1-BOCprotected
Packaging
1g
Price
$48
Updated
2021/12/16
SynQuest Laboratories
Product number
4H56-5-Q4
Product name
4-(2-Chloroethyl)piperazine, N1-Boc protected
Packaging
1g
Price
$53
Updated
2021/12/16
Matrix Scientific
Product number
046534
Product name
TERT-BUTYL 4-(2-CHLOROETHYL)PIPERAZINE-1-CARBOXYLATE
Purity
>95%
Packaging
5g
Price
$305
Updated
2021/12/16
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N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt Chemical Properties,Usage,Production

Uses

tert-Butyl 4-(2-Chloroethyl)piperazine-1-carboxylate is used in a study of anticancer activity of dihydroxyanthrathiazolediones.

Uses

By the direct condensation of chloroalkyl piperazine, nitrogen mustard benzaldehyde, and pyrrole anticancer activity to bel-7404 liver cancer cells was found.

Synthesis

107-04-0

57260-71-6

208167-83-3

General procedure for the synthesis of 1-BOC-4-(2-chloroethyl)piperazine from 1-bromo-2-chloroethane and N-BOC-piperazine: firstly, di-tert-butyl dicarbonate (18.98g, 87.07mmol) was added slowly and dropwise to the suspension of dipiperazine (30.00g, 348.27mmol) and sodium carbonate (106g, 348.27mmol) in dichloromethane (200ml) 87.07 mmol) in dichloromethane solution (30 ml), the titration process lasted for 1 hour and the reaction was carried out at room temperature. After completion of the dropwise addition, the reaction mixture was stirred at room temperature overnight. At the end of the reaction, the mixture was mixed with water (100 ml) and the organic phase was separated. The organic layer was dried with magnesium sulfate followed by evaporation under reduced pressure to remove the solvent. The residue was dissolved in dichloromethane (150 ml) and sodium carbonate (15.55 g, 146.77 mmol) and 1-bromo-2-chloroethane (21.05 g, 146.77 mmol) were added. The mixture was stirred at room temperature for one weekend. After completion of the reaction, the mixture was again mixed with water (100 ml) and the organic phase was separated. The organic layer was dried with magnesium sulfate and evaporated under reduced pressure to remove the solvent. Finally, the residue was purified by silica gel column chromatography using hexane and ethyl acetate as eluents to give 6.85 g of 1-Boc-4-(2-chloroethyl)piperazine.

References

[1] Patent: WO2014/145686, 2014, A2. Location in patent: Paragraph 0382-0383
[2] RSC Advances, 2015, vol. 5, # 125, p. 103172 - 103183

N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt Preparation Products And Raw materials

Raw materials

Preparation Products

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N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt Suppliers

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China
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View Lastest Price from N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt manufacturers

Career Henan Chemical Co
Product
N-Boc-N’-(2-Chloroethyl)piperazine, hydrochloride salt 208167-83-3
Price
US $1.00/KG
Min. Order
1g
Purity
99.0%
Supply Ability
100kg
Release date
2020-01-10

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