Skip to Content
Merck
All Photos(4)

Key Documents

View All Documentation

240230

Sigma-Aldrich

Phthalimide

≥99%

Synonym(s):

1,3-Dihydro-1,3-dioxoisoindole

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C8H5NO2
CAS Number:
85-41-6
Molecular Weight:
147.13
Beilstein:
118522
EC Number:
201-603-3
MDL number:
MFCD00005881
UNSPSC Code:
12352100
PubChem Substance ID:
24854410
NACRES:
NA.22

Quality Level

200

Assay

≥99%

mp

232-235 °C (lit.)

solubility

water: slightly soluble(lit.)

SMILES string

O=C1NC(=O)c2ccccc12

InChI

1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11)

InChI key

XKJCHHZQLQNZHY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Phthalimide was used in the synthesis of 6-amino agarose (AA) by Mitsunobu-inspired microwave mediated method.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

302.0 °F - closed cup

Flash Point(C)

150 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000399256
0000365873
0000305685
0000365873
0000305685

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

N-Bromophthalimide 95%

Sigma-Aldrich

260908

N-Bromophthalimide

N-(4-Bromobutyl)phthalimide 98%

Sigma-Aldrich

100919

N-(4-Bromobutyl)phthalimide

Alessio Pierini et al.
Journal of veterinary science, 21(5), e60-e60 (2020-10-06)
Tumor-associated neoangiogenesis is a crucial target for antitumor therapies. Thalidomide (TAL) is a promising anti-neoangiogenetic drug that has recently been used in the treatment of several malignancies in dogs. The aim of the study was to assess the pharmacokinetics of
Stalin Kondaveeti et al.
Carbohydrate polymers, 106, 365-373 (2014-04-12)
A facile 6-aminoagarose (AA) mediated synthesis of new fluorogenic amides of agarose with nicotinic (AA-NA) and picolinic acids (AA-PA) employing carbodiimide chemistry have been described. 6-Amino agarose (AA) was synthesized in a facile Mitsunobu-inspired microwave mediated method involving the reaction
Heloise Brice et al.
Chemical communications (Cambridge, England), 48(40), 4836-4838 (2012-04-14)
A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.
Binne Zwanenburg et al.
Bioorganic & medicinal chemistry, 19(24), 7394-7400 (2011-11-16)
A series of new strigolactone (SL) analogues is derived from simple and cheap starting materials. These SL analogues are designed using a working model. The first analogue is a modified Nijmegen-1, the second contains saccharin as substituent (bio-isosteric replacement of
Baocun Zhu et al.
Organic & biomolecular chemistry, 8(7), 1650-1654 (2010-03-20)
A highly selective ratiometric fluorescent probe, which contains an aminonaphthalimide fluorophore and a self-immolative spacer for 1,4-dithiothreitol (DTT) detection was designed and synthesized. The probe displays a 66 nm red-shift of fluorescence emission and the color changes from colorless to
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service