1875-48-5 | N-Aminophthalimide

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$13.00	$10.00
25g	98%	in stock	$28.00	$20.00
100g	98%	in stock	$105.00	$73.00

Description

• Catalog Number: AB61204
• Chemical Name: N-Aminophthalimide
• CAS Number: 1875-48-5
• Molecular Formula: C8H6N2O2
• Molecular Weight: 162.14544
• MDL Number: MFCD00005895
• SMILES: NN1C(=O)c2c(C1=O)cccc2

Computed Properties

• Complexity: 215
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.6

Literature

• Hypoiodite-mediated metal-free catalytic aziridination of alkenes.

  Angewandte Chemie (International ed. in English) 20120806

• 2-[(E)-(2-Hy-droxy-naphthalen-1-yl)methyl-idene-amino]-isoindoline-1,3-dione.

  Acta crystallographica. Section E, Structure reports online 20111201

• (E)-2-[(2-Chloro-benzyl-idene)amino]-isoindoline-1,3-dione.

  Acta crystallographica. Section E, Structure reports online 20111201

• Diastereoselective aziridination of 2-B(pin)-substituted allylic alcohols: an efficient approach to novel organoboron compounds.

  Organic letters 20111118

• 2-[(E)-(2,4-Dichloro-benzyl-idene)amino]-isoindoline-1,3-dione.

  Acta crystallographica. Section E, Structure reports online 20110701

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Novel Organotin(IV)-Schiff Base Complexes: Synthesis, Characterization, Antimicrobial Activity, and DNA Interaction Studies.

  Bioinorganic chemistry and applications 20100101

• A synergistic small-molecule combination directly eradicates diverse prion strain structures.

  Nature chemical biology 20091201

• The use of 3-aminophthalimide as a pro-chemiluminescent label in chemiluminescence and fluorescence-based cellular assays.

  Bioconjugate chemistry 20090201

• Aryl iodide mediated aziridination of alkenes.

  Organic letters 20051222

• Shape and position of 4-aminophthalimide (4-AP) time-resolved emission spectra (TRES) versus sodium dodecyl sulfate sds concentration in micellar solutions: the partitioning of 4-AP in the micellar phase and in water surrounding the micelles.

  The journal of physical chemistry. B 20050519

• Development of electrochemical processes for nitrene generation and transfer.

  The Journal of organic chemistry 20050204

• Electrochemical imination of sulfoxides using N-aminophthalimide.

  Organic letters 20020530

• Enantioselective aziridination of alkenes with N-aminophthalimide in the presence of lead tetraacetate-mediated chiral ligand.

  Organic letters 20020404

• Practical olefin aziridination with a broad substrate scope.

  Journal of the American Chemical Society 20020130

• A facile and highly diastereoselective aziridination of chiral camphor n-enoylpyrazolidinones with n-aminophthalimide.

  The Journal of organic chemistry 20010309