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N-Aminophthalimide

CAS No.:
1875-48-5
Catalog Number:
AG003GJG
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$100
- +
100g
98%
In Stock USA
United States
$294
- +
Product Description
Catalog Number:
AG003GJG
Chemical Name:
N-Aminophthalimide
CAS Number:
1875-48-5
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
MDL Number:
MFCD00005895
IUPAC Name:
2-aminoisoindole-1,3-dione
InChI:
InChI=1S/C8H6N2O2/c9-10-7(11)5-3-1-2-4-6(5)8(10)12/h1-4H,9H2
InChI Key:
KSILMCDYDAKOJD-UHFFFAOYSA-N
SMILES:
NN1C(=O)c2c(C1=O)cccc2
EC Number:
217-505-9
Properties
Complexity:
215  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
162.043g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
162.148g/mol
Monoisotopic Mass:
162.043g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
63.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  
Literature
Title Journal
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
Properties