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531-67-9,MFCD01572939
Catalog No.:AA00I9EL

531-67-9 | 2,2-Bipiperidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$13.00   $9.00
- +
250mg
95%
in stock  
$17.00   $12.00
- +
1g
95%
in stock  
$37.00   $26.00
- +
5g
95%
in stock  
$134.00   $94.00
- +
25g
95%
in stock  
$480.00   $336.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00I9EL
Chemical Name:
2,2-Bipiperidine
CAS Number:
531-67-9
Molecular Formula:
C10H20N2
Molecular Weight:
168.2792
MDL Number:
MFCD01572939
SMILES:
C1CCC(NC1)C1CCCCN1
Properties
Computed Properties
 
Complexity:
120  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
2  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Heterocycles,1989,vol.28,#1,p.121-124

[2]JournalofOrganicChemistry,2006,vol.71,#4,p.1523-1536

[3]Molecules,2015,vol.20,#2,p.1941-1954

[1]JournalofOrganicChemistry,1986,vol.51,#4,p.513-517

[2]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1985,p.895-898

[1]RSCAdvances,2016,vol.6,#90,p.87066-87081

[1]Heterocycles,1989,vol.28,#1,p.121-124

[1]Heterocycles,1989,vol.28,#1,p.121-124

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.2163,2165

[1]Heterocycles,1989,vol.28,p.121-124

[1]Heterocycles,1989,vol.28,p.121-124

[1]Heterocycles,1989,vol.28,p.121-124

[2]JournalofOrganicChemistry,2006,vol.71,p.1523-1536

[3]Molecules,2015,vol.20,p.1941-1954

[1]MagneticResonanceinChemistry,1990,vol.28,p.1035-1039

Literature

Title: Single-stranded oligonucleotide adducts formed by Pt complexes favoring left-handed base canting: steric effect of flanking residues and relevance to DNA adducts formed by Pt anticancer drugs.

Journal: Inorganic chemistry 20110905

Title: rac-2,2'-Bipiperidine-1,1'-diium dibromide.

Journal: Acta crystallographica. Section E, Structure reports online 20110601

Title: Origins of the distortions in the base pair step adjacent to platinum anticancer drug-DNA adducts. Fundamental NMR solution studies utilizing right-handed cross-link models having 5'- and 3'-flanking residues.

Journal: Journal of the American Chemical Society 20090902

Title: Marked dependence on carrier-ligand bulk but not on carrier-ligand chirality of the duplex versus single-strand forms of a DNA oligonucleotide with a series of G-Pt(II)-G intrastrand cross-links modeling cisplatin-DNA adducts.

Journal: Journal of the American Chemical Society 20051116

Title: Modification of second-sphere communication, leading to an unusually high abundance of the head-to-head conformer of cisplatin cross-link retro models.

Journal: Inorganic chemistry 20020211

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SDS
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Tags:531-67-9 Molecular Formula|531-67-9 MDL|531-67-9 SMILES|531-67-9 2,2-Bipiperidine
Catalog No.: AA00I9EL
531-67-9,MFCD01572939
531-67-9 | 2,2-Bipiperidine
Pack Size： 100mg
Purity： 95%
in stock
$13.00 $9.00
Pack Size： 250mg
Purity： 95%
in stock
$17.00 $12.00
Pack Size： 1g
Purity： 95%
in stock
$37.00 $26.00
Pack Size： 5g
Purity： 95%
in stock
$134.00 $94.00
Pack Size： 25g
Purity： 95%
in stock
$480.00 $336.00
Quantity
- +
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bulk Quotation Request
Technical Information
Catalog Number: AA00I9EL
Chemical Name: 2,2-Bipiperidine
CAS Number: 531-67-9
Molecular Formula: C10H20N2
Molecular Weight: 168.2792
MDL Number: MFCD01572939
SMILES: C1CCC(NC1)C1CCCCN1
Properties
Complexity: 120  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 2  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.2  
Upstream Synthesis Route
110-89-4    531-67-9 

[1]Heterocycles,1989,vol.28,#1,p.121-124

[2]JournalofOrganicChemistry,2006,vol.71,#4,p.1523-1536

[3]Molecules,2015,vol.20,#2,p.1941-1954

366-18-7    531-67-9 

[1]JournalofOrganicChemistry,1986,vol.51,#4,p.513-517

[2]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1985,p.895-898

110-89-4    1121-60-4    536-74-3    531-67-9    5337-53-1 

[1]RSCAdvances,2016,vol.6,#90,p.87066-87081

110-82-7    56528-77-9    3319-01-5    531-67-9    92-51-3 

[1]Heterocycles,1989,vol.28,#1,p.121-124

110-89-4    110-82-7    56528-77-9    3319-01-5    531-67-9    92-51-3 

[1]Heterocycles,1989,vol.28,#1,p.121-124

Downstream Synthesis Route
531-67-9    54824-86-1 

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.2163,2165

110-89-4    56528-77-9    3319-01-5    531-67-9    92-51-3 

[1]Heterocycles,1989,vol.28,p.121-124

110-89-4    110-82-7    56528-77-9    3319-01-5    531-67-9    92-51-3 

[1]Heterocycles,1989,vol.28,p.121-124

110-89-4    531-67-9 

[1]Heterocycles,1989,vol.28,p.121-124

[2]JournalofOrganicChemistry,2006,vol.71,p.1523-1536

[3]Molecules,2015,vol.20,p.1941-1954

531-67-9    555-16-8    18700-70-4    18700-70-4    18700-70-4 

[1]MagneticResonanceinChemistry,1990,vol.28,p.1035-1039

Literature fold

Title: Single-stranded oligonucleotide adducts formed by Pt complexes favoring left-handed base canting: steric effect of flanking residues and relevance to DNA adducts formed by Pt anticancer drugs.

Journal: Inorganic chemistry20110905

Title: rac-2,2'-Bipiperidine-1,1'-diium dibromide.

Journal: Acta crystallographica. Section E, Structure reports online20110601

Title: Origins of the distortions in the base pair step adjacent to platinum anticancer drug-DNA adducts. Fundamental NMR solution studies utilizing right-handed cross-link models having 5'- and 3'-flanking residues.

Journal: Journal of the American Chemical Society20090902

Title: Marked dependence on carrier-ligand bulk but not on carrier-ligand chirality of the duplex versus single-strand forms of a DNA oligonucleotide with a series of G-Pt(II)-G intrastrand cross-links modeling cisplatin-DNA adducts.

Journal: Journal of the American Chemical Society20051116

Title: Modification of second-sphere communication, leading to an unusually high abundance of the head-to-head conformer of cisplatin cross-link retro models.

Journal: Inorganic chemistry20020211

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