Phthalimide, N-trityloxy-

Base Information

Chemical Name:Phthalimide, N-trityloxy-
CAS No.:31938-10-0
Molecular Formula:C27H19 N O3
Molecular Weight:405.453
Hs Code.:2925190090
DSSTox Substance ID:DTXSID10185776
Nikkaji Number:J50.526I
Wikidata:Q83056876
Mol file:31938-10-0.mol

Synonyms:Phthalimide, N-trityloxy-;2-trityloxyisoindole-1,3-dione;31938-10-0;BRN 1554584;N-(Triphenylmethoxy)phthalimide;Phthalimide, N-triphenylmethoxy-;N-(Trityloxy)phthalimide;2-(Trityloxy)isoindoline-1,3-dione;C27H19NO3;5-21-11-00103 (Beilstein Handbook Reference);2-(trityloxy)-1h-isoindole-1,3(2h)-dione;SCHEMBL2041972;DTXSID10185776;C27-H19-N-O3;AKOS002684749;LS-109524;1H-Isoindole-1,3(2H)-dione, 2-(triphenylmethoxy)-;2-(triphenylmethoxy)-2,3-dihydro-1H-isoindole-1,3-dione

Suppliers and Price of Phthalimide, N-trityloxy-

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

American Custom Chemicals Corporation
2-TRITYLOXY-ISOINDOLE-1,3-DIONE 95.00%
5MG
$ 496.27

Total 4 raw suppliers

Chemical Property of Phthalimide, N-trityloxy-

Chemical Property:

Vapor Pressure:3.75E-13mmHg at 25°C
Melting Point:170-171 °C
Boiling Point:573.4°Cat760mmHg
Flash Point:300.6°C
PSA：46.61000
Density:1.32g/cm³
LogP:5.14420
XLogP3:5.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:405.13649347
Heavy Atom Count:31
Complexity:573

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-TRITYLOXY-ISOINDOLE-1,3-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)ON4C(=O)C5=CC=CC=C5C4=O

Technology Process of Phthalimide, N-trityloxy-

There total 4 articles about Phthalimide, N-trityloxy- 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: 99.0%

: 524-38-9
N-hydroxyphthalimide

: 76-83-5
trityl chloride

: 31938-10-0
2-(trityloxy)isoindoline-1,3-dione

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; for 36h;
DOI:10.1021/jo049617f

Reference yield:

: 524-38-9
N-hydroxyphthalimide

: 596-43-0
bromo-triphenyl-methane

: 31938-10-0
2-(trityloxy)isoindoline-1,3-dione

Guidance literature:: N-hydroxyphthalimide; With triethylamine; In N,N-dimethyl-formamide;

bromo-triphenyl-methane; In N,N-dimethyl-formamide; at 20 ℃;