N-Carbethoxyphthalimide

Base Information

Chemical Name:N-Carbethoxyphthalimide
CAS No.:22509-74-6
Deprecated CAS:2632247-56-2
Molecular Formula:C11H9NO4
Molecular Weight:219.197
Hs Code.:29251995
European Community (EC) Number:245-048-5
NSC Number:76576
UNII:DGO9NPX8LS
DSSTox Substance ID:DTXSID7066805
Nikkaji Number:J26.042H
Mol file:22509-74-6.mol

Synonyms:N-CARBETHOXYPHTHALIMIDE;22509-74-6;N-Ethoxycarbonylphthalimide;N-Carboethoxyphthalimide;N-(Ethoxycarbonyl)phthalimide;Ethyl N-phthaloylcarbamate;2H-Isoindole-2-carboxylic acid, 1,3-dihydro-1,3-dioxo-, ethyl ester;Phthalimide-N-carbethoxy;ethyl 1,3-dioxoisoindole-2-carboxylate;ethyl 1,3-dioxoisoindoline-2-carboxylate;N-Karbetoksi-ftalimid;2-Isoindolinecarboxylic acid, 1,3-dioxo-, ethyl ester;MFCD00005893;NSC 76576;DGO9NPX8LS;N-Karbetoksi-ftalimid [Yugoslavian];EINECS 245-048-5;BRN 0196340;AI3-52139;NSC-76576;Ethyl 1,3-dihydro-1,3-dioxo-2H-isoindole-2-carboxylate;Ethyl 1,3-dioxo-1,3-dihydro-2H-isoindole-2-carboxylate;ethyl 1,3-dioxo-2,3-dihydro-1H-isoindole-2-carboxylate;1,3-Dioxo-1,3-dihydro-isoindole-2-carboxylic acid ethyl ester;5-21-10-00428 (Beilstein Handbook Reference);1,3-DIOXO-2-ISOINDOLINECARBOXYLIC ACID ETHYL ESTER;N-carbetoxyphthalimide;Ethyl 1,3-dioxo-2-isoindolinecarboxylate;N -carbethoxyphthalimide;N-carbethoxy-phthalimide;N-carbethoxyphthal imide;N-carbethoxyphthal-imide;NEFKENS' REAGENT;N-Carbethoxy phthalimide;UNII-DGO9NPX8LS;n-carboethoxy phthalimide;N-carboethoxy-phthalimide;N-ethoxycarbonylphtalimide;REAGENTS, NEFKENS';N-(carbethoxy) phthalimide;N-(carbethoxy)-phthalimide;N-ethoxycarbonyl phthalimide;N-Ethoxycarobonylphthalimide;SCHEMBL74973;N-(ethoxycarbonyl) phthalimide;N-Carbethoxyphthalimide, 96%;DTXSID7066805;2-(CARBETHOXY)PHTHALIMIDE;AMY10366;NSC76576;N-(ETHOXYCARBONYL)-PHTHALIMIDE;AKOS005067960;AC-7768;AS-46867;BP-30091;LS-84705;SY039912;Ethyl 1,3-dioxo-2-iso-indolinecarboxylate;PHTHALIC ACID,IMIDE,N-ETHOXYCARBONYL;A4818;CS-0013033;FT-0638239;FT-0650429;F10775;2-Isoindolinecarboxylic acid,3-dioxo-, ethyl ester;J-014744;J-523557;ethyl 1,3-dioxo-1,3-dihydro-2H-isoindol-2-carboxylate;Ethyl 1,3-dioxo-1,3-dihydro-2H-isoindole-2-carboxylate #;ETHYL 1,3-DIOXO-1,3-DIHYDROISOINDOLE-2-CARBOXYLATE;2H-Isoindole-2-carboxylic acid,3-dihydro-1,3-dioxo-, ethyl ester;1,3-DIOXO-1,3-DIHYDROISOINDOLE-2-CARBOXYLIC ACID ETHYL ESTER

Suppliers and Price of N-Carbethoxyphthalimide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
N-Carbethoxyphthalimide
1g
$ 312.00

TRC
N-Carbethoxyphthalimide
10g
$ 90.00

TRC
N-Carbethoxyphthalimide
5g
$ 60.00

TCI Chemical
N-Ethoxycarbonylphthalimide [for Peptide Synthesis] >98.0%(N)
25g
$ 36.00

TCI Chemical
N-Ethoxycarbonylphthalimide [for Peptide Synthesis] >98.0%(N)
500g
$ 291.00

TCI Chemical
N-Ethoxycarbonylphthalimide [for Peptide Synthesis] >98.0%(N)
100g
$ 97.00

SynQuest Laboratories
N-Ethoxycarbonylphthalimide
25 g
$ 118.00

SynQuest Laboratories
N-Ethoxycarbonylphthalimide
1 g
$ 15.00

SynQuest Laboratories
N-Ethoxycarbonylphthalimide
5 g
$ 29.00

Sigma-Aldrich
N-Carbethoxyphthalimide 96%
25g
$ 36.20

Total 88 raw suppliers

Chemical Property of N-Carbethoxyphthalimide

Chemical Property:

Appearance/Colour:White crystalline powder
Vapor Pressure:3.48E-05mmHg at 25°C
Melting Point:90-92 °C
Refractive Index:1.594
Boiling Point:353.871 °C at 760 mmHg
PKA:-3.02±0.20(Predicted)
Flash Point:167.815 °C
PSA：63.68000
Density:1.398 g/cm³
LogP:1.37700
Storage Temp.:0-6°C
Solubility.:DMSO (Slightly), Methanol (Slightly)
Water Solubility.:insoluble
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:219.05315777
Heavy Atom Count:16
Complexity:315

Purity/Quality:

99% ^*data from raw suppliers

N-Carbethoxyphthalimide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-36/37/38-20/21/22
Safety Statements: 22-24/25-36/37/39-26-36

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Nitrogen Compounds -> Other Nitrogen Rings
Canonical SMILES:CCOC(=O)N1C(=O)C2=CC=CC=C2C1=O
Uses N-Carbethoxyphthalimide is used in the synthetic preparation of a novel dual binders as potent, selective, and orally bioavailable tankyrase inhibitors.

Technology Process of N-Carbethoxyphthalimide

There total 3 articles about N-Carbethoxyphthalimide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%