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About This Item
Empirical Formula (Hill Notation):
C8H6N2O2
CAS Number:
Molecular Weight:
162.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-505-9
Beilstein/REAXYS Number:
383756
MDL number:
Assay:
90%
Form:
powder
grade
technical grade
Quality Level
assay
90%
form
powder
mp
200-202 °C (lit.)
functional group
imide
SMILES string
NN1C(=O)c2ccccc2C1=O
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
Application
N-Aminophthalimide was employed in the aziridination of chiral N-enoyl sultams. It was also used in the synthesis of n-phthalimidoaziridines.
Other Notes
Remainder phthalhydrazide
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Journal of the Chemical Society. Chemical Communications, 1074-1074 (1993)
Kung-Shou Yang et al.
Organic letters, 4(7), 1107-1109 (2002-04-02)
[reaction: see text] Reaction of various N-enoyl oxazolidinones 5a-f with N-aminophthalimide and lead tetraacetate in the presence of camphor-derived chiral ligands provides the desired N-phthalimidoaziridines 6a-f in good to high enantiomeric excess (67-95% ee) at 0 degrees C within 15
Global Trade Item Number
| SKU | GTIN |
|---|---|
| PH006477-5MG | 04061822832527 |
| 178314-5G | 04061831809930 |
| 178314-25G | 04061831818994 |

