57260-71-6,MFCD00075265
Catalog No.:AA0035K2

57260-71-6 | t-Butyl piperazine-1-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
99%
in stock  
$5.00   $3.00
- +
10g
99%
in stock  
$6.00   $4.00
- +
25g
99%
in stock  
$8.00   $5.00
- +
100g
99%
in stock  
$18.00   $12.00
- +
250g
99%
in stock  
$43.00   $30.00
- +
500g
99%
in stock  
$80.00   $56.00
- +
1kg
99%
in stock  
$140.00   $98.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035K2
Chemical Name:
t-Butyl piperazine-1-carboxylate
CAS Number:
57260-71-6
Molecular Formula:
C9H18N2O2
Molecular Weight:
186.2514
MDL Number:
MFCD00075265
SMILES:
O=C(N1CCNCC1)OC(C)(C)C
Properties
Properties
 
BP:
98-100  
Form:
Solid  
MP:
43-47 °C(lit.)  
Stability:
Air Sensitive  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.5  

Synonyms
 
  
Literature

Title: Photoaddition of N-substituted piperazines to C60: an efficient approach to the synthesis of water-soluble fullerene derivatives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20060717

Title: Ruthenium-catalyzed anti-Markovnikov hydroamination of vinylarenes.

Journal: Journal of the American Chemical Society 20040310

Title: Intermolecular, markovnikov hydroamination of vinylarenes with alkylamines.

Journal: Journal of the American Chemical Society 20031126

Title: Rhodium-catalyzed anti-Markovnikov hydroamination of vinylarenes.

Journal: Journal of the American Chemical Society 20030514

Title: Progress in arylpiperazine synthesis by the catalytic amination reaction.

Journal: Bioorganic & medicinal chemistry 20021201

Title: Binbin Cheng, et al. Discovery of novel resorcinol diphenyl ether-based PROTAC-like molecules as dual inhibitors and degraders of PD-L1. Eur J Med Chem. 2020;199:112377.

Application
1-Boc-piperazine is utilized in Buchwald-Hartwig amination reactions with aryl halides, yielding various amine derivatives. It serves as a key intermediate in the synthesis of monosubstituted piperazine compounds found in bioactive molecules and drugs like trazodone.
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SDS
Tags:57260-71-6 Molecular Formula|57260-71-6 MDL|57260-71-6 SMILES|57260-71-6 t-Butyl piperazine-1-carboxylate
Catalog No.: AA0035K2
57260-71-6,MFCD00075265
57260-71-6 | t-Butyl piperazine-1-carboxylate
Pack Size: 5g
Purity: 99%
in stock
$5.00 $3.00
Pack Size: 10g
Purity: 99%
in stock
$6.00 $4.00
Pack Size: 25g
Purity: 99%
in stock
$8.00 $5.00
Pack Size: 100g
Purity: 99%
in stock
$18.00 $12.00
Pack Size: 250g
Purity: 99%
in stock
$43.00 $30.00
Pack Size: 500g
Purity: 99%
in stock
$80.00 $56.00
Pack Size: 1kg
Purity: 99%
in stock
$140.00 $98.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0035K2
Chemical Name: t-Butyl piperazine-1-carboxylate
CAS Number: 57260-71-6
Molecular Formula: C9H18N2O2
Molecular Weight: 186.2514
MDL Number: MFCD00075265
SMILES: O=C(N1CCNCC1)OC(C)(C)C
Properties
BP: 98-100  
Form: Solid  
MP: 43-47 °C(lit.)  
Stability: Air Sensitive  
Storage: Room Temperature;  
Complexity: 181  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.5  
265:   
Literature fold

Title: Photoaddition of N-substituted piperazines to C60: an efficient approach to the synthesis of water-soluble fullerene derivatives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20060717

Title: Ruthenium-catalyzed anti-Markovnikov hydroamination of vinylarenes.

Journal: Journal of the American Chemical Society20040310

Title: Intermolecular, markovnikov hydroamination of vinylarenes with alkylamines.

Journal: Journal of the American Chemical Society20031126

Title: Rhodium-catalyzed anti-Markovnikov hydroamination of vinylarenes.

Journal: Journal of the American Chemical Society20030514

Title: Progress in arylpiperazine synthesis by the catalytic amination reaction.

Journal: Bioorganic & medicinal chemistry20021201

Title: Binbin Cheng, et al. Discovery of novel resorcinol diphenyl ether-based PROTAC-like molecules as dual inhibitors and degraders of PD-L1. Eur J Med Chem. 2020;199:112377.

Application fold
1-Boc-piperazine is utilized in Buchwald-Hartwig amination reactions with aryl halides, yielding various amine derivatives. It serves as a key intermediate in the synthesis of monosubstituted piperazine compounds found in bioactive molecules and drugs like trazodone.
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