2516-34-9,MFCD00001328
Catalog No.:AA002QMJ

2516-34-9 | Cyclobutylamine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$25.00   $17.00
- +
5g
98%
in stock  
$68.00   $47.00
- +
100g
98%
in stock  
$1,115.00 $780.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002QMJ
Chemical Name:
Cyclobutylamine
CAS Number:
2516-34-9
Molecular Formula:
C4H9N
Molecular Weight:
71.1210
MDL Number:
MFCD00001328
SMILES:
NC1CCC1
Properties
Properties
 
BP:
81.5 °C752 mm Hg(lit.)  
Form:
Liquid  
Refractive Index:
n20/D 1.437(lit.)  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
30.6  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.2  

Literature

Title: Searching for new cell-penetrating agents: hybrid cyclobutane-proline γ,γ-peptides.

Journal: Organic & biomolecular chemistry 20120528

Title: A 1H NMR and theoretical investigation of the conformations of some monosubstituted cyclobutanes.

Journal: Magnetic resonance in chemistry : MRC 20110101

Title: Synthesis of highly substituted cyclobutane fused-ring systems from N-vinyl beta-lactams through a one-pot domino process.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100406

Title: Bis(2-cyclo-butyl-imino-methyl-4,6-dihydro-seleno-phenolato)zinc(II).

Journal: Acta crystallographica. Section E, Structure reports online 20090901

Title: Selective Michael-aldol reaction by use of sterically hindered aluminum aryloxides as Lewis acids: an easy approach to cyclobutane amino acids.

Journal: Organic letters 20050804

Title: Effect on K(ATP) channel activation properties and tissue selectivity of the nature of the substituent in the 7- and the 3-position of 4H-1,2,4-benzothiadiazine 1,1-dioxides.

Journal: Journal of medicinal chemistry 20050519

Title: Effect of mobile phase amine additives on enantioselectivity for phenylalanine analogs.

Journal: Journal of chromatography. A 20010824

Title: Discovery of 4-[3-(trans-3-dimethylaminocyclobutyl)-1H-indol-5-ylmethyl]-(4S)-oxazolidin-2-one (4991W93), a 5HT(1B/1D) receptor partial agonist and a potent inhibitor of electrically induced plasma extravasation.

Journal: Journal of medicinal chemistry 20010301

Title: Platinum(II) and palladium(II) complexes with dithiocarbamates and amines: synthesis, characterization and cell assay.

Journal: Journal of inorganic biochemistry 20010101

Title: Antiviral activities of nucleosides and nucleotides against wild-type and drug-resistant strains of murine cytomegalovirus.

Journal: Antiviral research 19950101

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SDS
Tags:2516-34-9 Molecular Formula|2516-34-9 MDL|2516-34-9 SMILES|2516-34-9 Cyclobutylamine
Catalog No.: AA002QMJ
2516-34-9,MFCD00001328
2516-34-9 | Cyclobutylamine
Pack Size: 1g
Purity: 98%
in stock
$25.00 $17.00
Pack Size: 5g
Purity: 98%
in stock
$68.00 $47.00
Pack Size: 100g
Purity: 98%
in stock
$1,115.00 $780.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA002QMJ
Chemical Name: Cyclobutylamine
CAS Number: 2516-34-9
Molecular Formula: C4H9N
Molecular Weight: 71.1210
MDL Number: MFCD00001328
SMILES: NC1CCC1
Properties
BP: 81.5 °C752 mm Hg(lit.)  
Form: Liquid  
Refractive Index: n20/D 1.437(lit.)  
Stability: Hygroscopic  
Storage: Inert atmosphere;-20 ℃;  
Complexity: 30.6  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 5  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.2  
Literature fold

Title: Searching for new cell-penetrating agents: hybrid cyclobutane-proline γ,γ-peptides.

Journal: Organic & biomolecular chemistry20120528

Title: A 1H NMR and theoretical investigation of the conformations of some monosubstituted cyclobutanes.

Journal: Magnetic resonance in chemistry : MRC20110101

Title: Synthesis of highly substituted cyclobutane fused-ring systems from N-vinyl beta-lactams through a one-pot domino process.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20100406

Title: Bis(2-cyclo-butyl-imino-methyl-4,6-dihydro-seleno-phenolato)zinc(II).

Journal: Acta crystallographica. Section E, Structure reports online20090901

Title: Selective Michael-aldol reaction by use of sterically hindered aluminum aryloxides as Lewis acids: an easy approach to cyclobutane amino acids.

Journal: Organic letters20050804

Title: Effect on K(ATP) channel activation properties and tissue selectivity of the nature of the substituent in the 7- and the 3-position of 4H-1,2,4-benzothiadiazine 1,1-dioxides.

Journal: Journal of medicinal chemistry20050519

Title: Effect of mobile phase amine additives on enantioselectivity for phenylalanine analogs.

Journal: Journal of chromatography. A20010824

Title: Discovery of 4-[3-(trans-3-dimethylaminocyclobutyl)-1H-indol-5-ylmethyl]-(4S)-oxazolidin-2-one (4991W93), a 5HT(1B/1D) receptor partial agonist and a potent inhibitor of electrically induced plasma extravasation.

Journal: Journal of medicinal chemistry20010301

Title: Platinum(II) and palladium(II) complexes with dithiocarbamates and amines: synthesis, characterization and cell assay.

Journal: Journal of inorganic biochemistry20010101

Title: Antiviral activities of nucleosides and nucleotides against wild-type and drug-resistant strains of murine cytomegalovirus.

Journal: Antiviral research19950101

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