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ChemicalBook--->CAS DataBase List--->57260-71-6

57260-71-6

57260-71-6 Structure

57260-71-6 Structure
IdentificationMore
[Name]

tert-Butyl 1-piperazinecarboxylate
[CAS]

57260-71-6
[Synonyms]

1-BOC-PIPERAZINE
1-N-BOC-PIPERAZINE
1-(TERT-BUTOXYCARBONYL)PIPERAZINE
BOC-PAZ
BOC-PIPERAZINE
BUTTPARK 52\11-35
N-BOC-PIPERAZINE
N-(T-BOC)PIPERAZINE
N-T-BUTOXYCARBONYLPIPERAZINE
N-(TERT-BUTOXYCARBONYL)PIPERAZINE
N-(TERT-BUTYLOXYCARBONYL)-PIPERAZINE
PIBOC
PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
RARECHEM AR PA 0026
TERT-BUTYL 1-PIPERAZINECARBOXYLATE
TERT-BUTYL N-PIPERAZINE
TERT-BUTYL PIPERAZINE-1-CARBOXYLATE
TERT-BUTYL TETRAHYDROPYRAZINE-1(2H)-CARBOXYLATE
t-Butyl 1-piperazincarboxylate
1-(tert-Butoxycarbonyl)piperazine~tert-Butyl 1-piperazinecarboxylate
[EINECS(EC#)]

611-489-0
[Molecular Formula]

C9H18N2O2
[MDL Number]

MFCD00075265
[Molecular Weight]

186.25
[MOL File]

57260-71-6.mol
Chemical PropertiesBack Directory
[Appearance]

Waxy Solid
[Melting point ]

43-47 °C(lit.)
[Boiling point ]

98-100
[density ]

1.030±0.06 g/cm3(Predicted)
[Fp ]

>230 °F
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[solubility ]

Soluble in DMSO
[form ]

Low Melting Crystalline Mass
[pka]

8.45±0.10(Predicted)
[color ]

White to light yellow
[Water Solubility ]

Soluble in ethyl acetate, methanol and water.
[Sensitive ]

Air Sensitive
[Detection Methods]

MS,NMR,HPLC
[BRN ]

879985
[InChIKey]

CWXPZXBSDSIRCS-UHFFFAOYSA-N
[CAS DataBase Reference]

57260-71-6(CAS DataBase Reference)
[NIST Chemistry Reference]

T-butyl 1-piperaziencarboxylate(57260-71-6)
Questions And AnswerBack Directory
[Uses]

N-Boc-piperazine is a compound useful in organic synthesis.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

3263
[WGK Germany ]

3
[F ]

3-10-34
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29335900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium hydroxide-->Methanol-->Dichloromethane-->PETROLEUM ETHER-->Di-tert-butyl dicarbonate-->Piperazine
[Preparation Products]

1-Boc-4-(2-formylphenyl)piperazine-->1-(CYCLOPROPYLMETHYL)PIPERAZINE-->1-(2-Methoxyethyl)piperazine-->N-Boc-4-(Cyclopropylmethyl)piperazine-->1-BOC-4-(4-FORMYLPHENYL)PIPERAZINE-->1-(2-PYRAZINYL)-PIPERAZINE-->tert-Butyl 4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazine-1-carboxylate ,97%-->1-(3-Chlorphenyl)piperazine-->TERT-BUTYL 4-(5-FORMYLPYRID-2-YL)PIPERAZINE-1-CARBOXYLATE-->PIPERAZINE-1,4-DICARBOXYLIC ACID TERT-BUTYL ESTER METHYL ESTER-->1303512-02-8-->4-(2-BROMO-PHENYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER-->4-(5-AMINOPYRIDIN-2-YL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER-->4-(2-BROMOETHYL)-1-PIPERAZINECARBOXYLIC ACID, 1,1-DIMETHYLETHYL ESTER-->4-(3-AMINO-PHENYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER-->Trimetazidine
Hazard InformationBack Directory
[Chemical Properties]

Waxy Solid
[Application]

Tert-Butyl 1-piperazinecarboxylate, also known as Olaparib Impurity 7, is an impurity of Olaparib. Olaparib is used alone or in combination with bevacizumab (Avastin) to help maintain the response of certain types of ovarian (female reproductive organs where eggs are formed), fallopian tube (tube that transports eggs released by the ovaries to the uterus), and peritoneal (layer of tissue that lines the abdomen) cancer in people who have completely responded or partially responded to their first or later chemotherapy treatments. Olaparib is also used to treat certain types of breast cancer that has spread to other parts of the body and has not improved or has worsened after treatment with other therapies. It is also used to treat certain types of early breast cancer in people who have already been treated with other chemotherapy treatments.
[General Description]

1-Boc-piperazine is an N-Boc protected piperazine. Crosscoupling of 1-Boc-piperazine with aryl iodides using CuBr/1,1′-bi-2-naphthol (catalyst) and K3PO4 (base) has been reported. 1-Boc-piperazine undergoes Buchwald-Hartwig coupling reactions with aryl halides. 1-Boc-piperazine can be prepared in 80% yield via solvent-free N-Boc protection catalyzed by iodine.
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 1-piperazinecarboxylate(57260-71-6)1HNMR
tert-Butyl 1-piperazinecarboxylate(57260-71-6)FT-IR
tert-Butyl 1-piperazinecarboxylate(57260-71-6)IR
tert-Butyl 1-piperazinecarboxylate(57260-71-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

tert-Butyl 1-piperazinecarboxylate, 97%(57260-71-6)
[Alfa Aesar]

1-Boc-piperazine, 99%(57260-71-6)
[Sigma Aldrich]

57260-71-6(sigmaaldrich)
[TCI AMERICA]

1-(tert-Butoxycarbonyl)piperazine,>98.0%(GC)(T)(57260-71-6)
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