2762-32-5,MFCD00132878
Catalog No.:AA002U6O

2762-32-5 | Piperazine-2-carboxylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$8.00   $6.00
- +
25g
97%
in stock  
$22.00   $16.00
- +
100g
97%
in stock  
$61.00   $43.00
- +
500g
97%
in stock  
$303.00   $212.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002U6O
Chemical Name:
Piperazine-2-carboxylic acid
CAS Number:
2762-32-5
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
MDL Number:
MFCD00132878
SMILES:
OC(=O)C1CNCCN1
Properties
Properties
 
BP:
313.6 °C at 760 mmHg  
Form:
Solid  
MP:
291-293 oC (dec.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
116  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-3.5  

Synonyms
 
  
Upstream Synthesis Route

[1]TetrahedronLetters,1989,vol.30,#39,p.5193-5196

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,#8,p.1121-1126

[3]Patent:US6251919,2001,B1,

[1]TetrahedronLetters,1981,vol.22,p.141-144

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#23,p.4241-4244

[2]Patent:WO2018/26782,2018,A1,.Locationinpatent:Page/Pagecolumn51-52

[3]Patent:WO2006/105262,2006,A1,.Locationinpatent:Page/Pagecolumn82;83

[1]Patent:US5157041,1992,A,

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#23,p.4241-4244

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,#8,p.1121-1126

[3]Patent:US6251919,2001,B1,

Downstream Synthesis Route

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.1121-1126

[3]Patent:US6251919,2001,B1

[1]JournalofMedicinalChemistry,1981,vol.24,p.93-101

2762-32-5    7677-24-9   
TMS-DL-(N)Pip-OTMS 

[1]BulletindesSocietesChimiquesBelges,1988,vol.97,p.48-50

2762-32-5    58632-95-4   
4-(2-tert-Butoxy-acetyl)-piperazine-2-carboxylicacid 

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

Literature

Title: High-performance liquid chromatographic enantioseparation of unusual secondary amino acids on a D-penicillamine-based chiral ligand exchange column.

Journal: Chirality 20060801

Title: S-stereoselective piperazine-2-tert-butylcarboxamide hydrolase from Pseudomonas azotoformans IAM 1603 is a novel L-amino acid amidase.

Journal: European journal of biochemistry 20040401

Title: A novel R-stereoselective amidase from Pseudomonas sp. MCI3434 acting on piperazine-2-tert-butylcarboxamide.

Journal: European journal of biochemistry 20040401

Title: Application of a new chiral derivatizing agent to the enantioseparation of secondary amino acids.

Journal: Journal of chromatography. A 20020301

Title: Chiral synthesis and enzymatic resolution of (S)-(-)piperazine-2-carboxylic acid using enzyme alcalase.

Journal: Enantiomer 20010101

Quotation Request
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Additional Info:
SDS
Tags:2762-32-5 Molecular Formula|2762-32-5 MDL|2762-32-5 SMILES|2762-32-5 Piperazine-2-carboxylic acid
Catalog No.: AA002U6O
2762-32-5,MFCD00132878
2762-32-5 | Piperazine-2-carboxylic acid
Pack Size: 1g
Purity: 97%
in stock
$6.00 $4.00
Pack Size: 5g
Purity: 97%
in stock
$8.00 $6.00
Pack Size: 25g
Purity: 97%
in stock
$22.00 $16.00
Pack Size: 100g
Purity: 97%
in stock
$61.00 $43.00
Pack Size: 500g
Purity: 97%
in stock
$303.00 $212.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002U6O
Chemical Name: Piperazine-2-carboxylic acid
CAS Number: 2762-32-5
Molecular Formula: C5H10N2O2
Molecular Weight: 130.1451
MDL Number: MFCD00132878
SMILES: OC(=O)C1CNCCN1
Properties
BP: 313.6 °C at 760 mmHg  
Form: Solid  
MP: 291-293 oC (dec.)  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 116  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
XLogP3: -3.5  
73:   
Upstream Synthesis Route
98-97-5    2762-32-5 

[1]TetrahedronLetters,1989,vol.30,#39,p.5193-5196

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,#8,p.1121-1126

[3]Patent:US6251919,2001,B1,

77873-75-7    2762-32-5 

[1]TetrahedronLetters,1981,vol.22,p.141-144

2762-32-5    24424-99-5    128019-59-0 

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#23,p.4241-4244

[2]Patent:WO2018/26782,2018,A1,.Locationinpatent:Page/Pagecolumn51-52

[3]Patent:WO2006/105262,2006,A1,.Locationinpatent:Page/Pagecolumn82;83

2762-32-5    128019-59-0 

[1]Patent:US5157041,1992,A,

2762-32-5    129799-08-2 

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#23,p.4241-4244

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,#8,p.1121-1126

[3]Patent:US6251919,2001,B1,

Downstream Synthesis Route
98-97-5    2762-32-5 

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

[2]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.1121-1126

[3]Patent:US6251919,2001,B1

2762-32-5    1448-87-9    55686-43-6 

[1]JournalofMedicinalChemistry,1981,vol.24,p.93-101

2762-32-5    7677-24-9   
TMS-DL-(N)Pip-OTMS 

[1]BulletindesSocietesChimiquesBelges,1988,vol.97,p.48-50

2762-32-5    58632-95-4   
4-(2-tert-Butoxy-acetyl)-piperazine-2-carboxylicacid 

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

2762-32-5    112221-15-5    126937-47-1 

[1]TetrahedronLetters,1989,vol.30,p.5193-5196

Literature fold

Title: High-performance liquid chromatographic enantioseparation of unusual secondary amino acids on a D-penicillamine-based chiral ligand exchange column.

Journal: Chirality20060801

Title: S-stereoselective piperazine-2-tert-butylcarboxamide hydrolase from Pseudomonas azotoformans IAM 1603 is a novel L-amino acid amidase.

Journal: European journal of biochemistry20040401

Title: A novel R-stereoselective amidase from Pseudomonas sp. MCI3434 acting on piperazine-2-tert-butylcarboxamide.

Journal: European journal of biochemistry20040401

Title: Application of a new chiral derivatizing agent to the enantioseparation of secondary amino acids.

Journal: Journal of chromatography. A20020301

Title: Chiral synthesis and enzymatic resolution of (S)-(-)piperazine-2-carboxylic acid using enzyme alcalase.

Journal: Enantiomer20010101

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