Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-

Base Information

Chemical Name:Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-
CAS No.:64489-90-3
Molecular Formula:C₁₈H₁₇NO₂
Molecular Weight:279.338
Hs Code.:
NSC Number:94837
DSSTox Substance ID:DTXSID20294161
Wikidata:Q82033279

Synonyms:64489-90-3;Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-;NSC94837;2-(2,4,6-Trimethylbenzyl)isoindoline-1,3-dione;1H-Isoindole-1,3(2H)-dione, 2-[(2,4,6-trimethylphenyl)methyl]-;2-[(2,4,6-trimethylphenyl)methyl]isoindole-1,3-dione;NCIOpen2_006244;SCHEMBL7894073;DTXSID20294161;NBYNEQBMCUMTLI-UHFFFAOYSA-N;NSC-94837;AKOS001755394;SR-01000091700;SR-01000091700-1;2-(MESITYLMETHYL)-1H-ISOINDOLE-1,3(2H)-DIONE;2-[(2,4,6-trimethylphenyl)methyl]-2,3-dihydro-1H-isoindole-1,3-dione

Suppliers and Price of Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-

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

Total 6 raw suppliers

Chemical Property of Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-

Chemical Property:

Vapor Pressure:8.18E-08mmHg at 25°C
Boiling Point:436.3°Cat760mmHg
Flash Point:191.9°C
Density:1.216g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:279.125928785
Heavy Atom Count:21
Complexity:397

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)C)CN2C(=O)C3=CC=CC=C3C2=O)C

Technology Process of Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)-

There total 2 articles about Isoindole-1,3-dione, 2-(2,4,6-trimethylbenzyl)- 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:

: 40393-99-5
(2,4,6-trimethylbenzyl)amine

: 1074-82-4
potassium phtalimide

: 64489-90-3
N-(2,4,6-trimethyl-benzyl)-phthalimide

Guidance literature:: at 180 ℃;
DOI:10.1021/ja01848a005

Reference yield:

: 64489-90-3
N-(2,4,6-trimethyl-benzyl)-phthalimide

Guidance literature:: Mesitylen, N-Hydroxymethyl-phthalimid;
DOI:10.1016/0040-4020(77)80088-4

Reference yield:

: 64489-90-3
N-(2,4,6-trimethyl-benzyl)-phthalimide

: N-(2,4,6-trimethyl-benzyl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous hydrobromic acid; acetic acid

With hydrogen bromide; acetic acid;
DOI:10.1021/ja01848a005