CAS 5455-98-1
:N-(2,3-Epoxypropyl)phthalimide
Description:
N-(2,3-Epoxypropyl)phthalimide, with the CAS number 5455-98-1, is an organic compound characterized by its epoxy and phthalimide functional groups. This substance typically appears as a white to off-white solid and is known for its reactivity due to the presence of the epoxy group, which can participate in various chemical reactions, including ring-opening and cross-linking processes. It is often utilized in the synthesis of polymers and as an intermediate in organic synthesis. The phthalimide moiety contributes to its stability and can influence its solubility in organic solvents. Additionally, this compound may exhibit properties such as thermal stability and resistance to certain chemicals, making it suitable for applications in coatings, adhesives, and sealants. Safety considerations should be taken into account, as it may pose health risks if inhaled or ingested, and appropriate handling procedures should be followed. Overall, N-(2,3-Epoxypropyl)phthalimide is a versatile compound with significant utility in various chemical applications.
Formula:C11H9NO3
InChI:InChI=1/C11H9NO3/c13-10-8-3-1-2-4-9(8)11(14)12(10)5-7-6-15-7/h1-4,7H,5-6H2
InChI key:InChIKey=DUILGEYLVHGSEE-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1CC3CO3)=CC=CC2
Synonyms:- (Phthalimidomethyl)Oxirane
- 1H-Isoindole-1,3(2H)-dione, 2-(2-oxiranylmethyl)-
- 1H-Isoindole-1,3(2H)-dione, 2-(oxiranylmethyl)-
- 2,3-Epoxypropylphthalimide
- 2-(2-Oxiranylmethyl)-1H-isoindole-1,3(2H)-dione
- 2-(Oxiran-2-Ylmethyl)-1H-Isoindole-1,3(2H)-Dione
- 2-(Oxiran-2-Ylmethyl)Isoindoline-1,3-Dione
- 2-(Oxiran-2-ylmethyl)-2,3-dihydro-1H-isoindole-1,3-dione
- 2-(Oxiran-2-ylmethyl)isoindole-1,3-dione
- 2-(Oxiranylmethyl)-1H-Isoindole-1,3(2H)-Dione
- 2-(Oxiranylmethyl)-1H-Isoindole-3(2H)-Dione
- 2-(Phthalimidomethyl)oxirane
- 2-[(Oxiranyl)methyl]isoindole-1,3-dione
- Denacol EX 731
- Denacolex731
- N-(2,3-Epoxypropan-1-yl)phthalimide
- N-(2,3-Epoxypropyl) Phthalmide
- N-(2,3-Epoxypropyl)-2-Phthalimide
- N-(2,3-Epoxypropyl)-O-Phthalimide
- N-(2,3-Epoxypropyl)-Phthalamide
- N-(2,3-Epoxypropyl)-Phthalimid
- N-Glycidylphthalimide
- N-Glycidyphthalimide
- N-Oxiranylmethylphthalimide
- NSC 7244
- Phthalimide, N-(2,3-epoxypropyl)-
- N-(2,3-Epoxypropyl)phthalimide
- N-Glycidylphthalimide,N-(2,3-Epoxypropyl)-o-Phthalimide
- N-(Oxiranylmethyl)phthalimide
- 2-Oxiranylmethyl-isoindole-1,3-dione
- 2-(Oxiranylmethyl)-2H-isoindole-1,3-dione
- See more synonyms
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Found 7 products.
N-(2,3-Epoxypropyl)phthalimide
CAS:Formula:C11H9NO3Purity:95%Color and Shape:SolidMolecular weight:203.19412-(Oxiran-2-ylmethyl)isoindoline-1,3-dione
CAS:2-(Oxiran-2-ylmethyl)isoindoline-1,3-dioneFormula:C11H9NO3Purity:99%Color and Shape: white crystalline powderMolecular weight:203.19406g/mol2-(Oxiran-2-ylmethyl)-1H-isoindole-1,3(2H)-dione
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:203.19700622558594N-Glycidyl Phthalimide
CAS:Controlled ProductFormula:C11H9NO3Color and Shape:NeatMolecular weight:203.19N-Glycidyl phthalimide
CAS:<p>N-Glycidyl phthalimide is a dithiocarbamic compound that has been shown to inhibit blood coagulation. It is synthesized by the reaction of chloroacetic acid with phthalic anhydride and glycine, which leads to the formation of a homochiral product. N-Glycidyl phthalimide has been shown to be effective in vivo in animal models and has biological relevance, as it can be enzymatically hydrolyzed to form 5-hydroxytetrahydrofolate, which is necessary for DNA synthesis. The rate enhancement of this process may be due to the carbonyl group on the molecule, which interacts with enzymes such as carboxypeptidase A and cathepsin C.</p>Formula:C11H9NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:203.19 g/mol






