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Phthalimide - 99%, high purity , CAS No.85-41-6
Basic Description
Synonyms
Phthalimide; Tafenoquine related; SKF-2450 | 1,3-Isoindoledione | isoindole-1,3(2H)-dione | AI3-07565 | folpet TP1 | FS-3820 | Phenylimide | STK299439 | DTXSID3026514 | 3-hydroxyisoindol-1-one | CHEBI:38817 | MFCD00005881 | O-Phthalimide | phtalimide | FT
Specifications & Purity
≥99%
Shipped In
Normal
Product Description
Phthalimide is a reagent used to transform allyl- and alkyl halides into protected primary amines.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Isoindoles and derivatives
Subclass
Isoindolines
Intermediate Tree Nodes
Isoindolones
Direct Parent
Phthalimides
Alternative Parents
Isoindoles Benzenoids N-unsubstituted carboxylic acid imides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phthalimide - Isoindole - Benzenoid - Carboxylic acid imide, n-unsubstituted - Carboxylic acid imide - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.
External Descriptors
phthalimides
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
504751176
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751176
IUPAC Name
isoindole-1,3-dione
INCHI
InChI=1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11)
InChIKey
XKJCHHZQLQNZHY-UHFFFAOYSA-N
Smiles
C1=CC=C2C(=C1)C(=O)NC2=O
Isomeric SMILES
C1=CC=C2C(=C1)C(=O)NC2=O
WGK Germany
1
RTECS
TI3920000
Molecular Weight
147.13
Beilstein
118522
Reaxy-Rn
118522
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=118522&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (1 mg/ml at 19.5 °C), aqueous alkali hydroxides, acetone (2.5%), and hot methanol.
Flash Point(°C)
150℃
Boil Point(°C)
366°C
Melt Point(°C)
238°C
Molecular Weight
147.130 g/mol
XLogP3
1.100
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
147.032 Da
Monoisotopic Mass
147.032 Da
Topological Polar Surface Area
46.200 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
190.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Liuqi Kong, Yan Zhu, Shaochen Sun, Hongye Li, Jiarui Wu, Farong Tao, Liping Wang, Guang Li.
(2023)
Tunable multicolor afterglow including white light emission from poly(acrylic acid)-based room temperature phosphorescence materials via phosphorescence FRET. DYES AND PIGMENTS,
214
(111242).
2.
Fan Ye, Liwei Shen, Shi Liu, Huanyu Liu, Xinyuan Zhang, Zejun Zhang, Ying Yang, Xuening Feng, Yuqi Tang, Dong Xiang, Yuanzhu Mi, Xuemin Yan.
(2022)
Demulsification of amphiphilic gemini ionic liquids and its demulsification mechanism. CHEMOSPHERE,
309
(136650).
3.
Xuecheng Zhang, Jun Gao, Qinghua Chu, Haixia Lyu, Zenghong Xie.
(2022)
Specific recognition and determination of trace phthalic acid esters by molecularly imprinted polymer based on metal organic framework. ANALYTICA CHIMICA ACTA,
1227
(340292).
4.
Ya-Mu Xia, Wen Zhang, Meng-Ying Li, Meng Xia, Li-Jia Zou, Wei-Wei Gao.
(2019)
Effective Electrochemical Determination of Chloramphenicol and Florfenicol Based on Graphene/Copper Phthalocyanine Nanocomposites Modified Glassy Carbon Electrode. JOURNAL OF THE ELECTROCHEMICAL SOCIETY,
166
(8):
(B654).
5.
Zhan Yi-zhen, Zhao Xue, Wang Wei.
(2017)
Synthesis and application of phthalimide disperse dyes. FIBERS AND POLYMERS,
18
(12):
(2278-2286).
6.
Yizhen Zhan, Xue Zhao, Wei Wang.
(2017)
Synthesis of phthalimide disperse dyes and study on the interaction energy. DYES AND PIGMENTS,
146
(240).
7.
Yan Xia, Guang Lu Han, Qiu Gen Zhang, Yi Gong, Ian Broadwell, Qing Lin Liu.
(2013)
CuO-filled aminomethylated polysulfone hybrid membranes for deep desulfurization. JOURNAL OF APPLIED POLYMER SCIENCE,
130
(5):
(3718-3725).
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7 Citations
C2513606