4,5,6,7-Tetrachlorophthalide

Base Information

Chemical Name:4,5,6,7-Tetrachlorophthalide
CAS No.:27355-22-2
Molecular Formula:C8H2 Cl4 O2
Molecular Weight:271.915
Hs Code.:2932209013
UNII:44IHE2M2T4
DSSTox Substance ID:DTXSID2058045
Nikkaji Number:J1.881C
Wikidata:Q27094229
Metabolomics Workbench ID:147829
ChEMBL ID:CHEMBL357452
Mol file:27355-22-2.mol

Synonyms:4,5,6,7-tetrachlorophthalide

Suppliers and Price of 4,5,6,7-Tetrachlorophthalide

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

TRC
Phthalide(Fthalide)
1mg
$ 165.00

American Custom Chemicals Corporation
4,5,6,7-TETRACHLOROISOBENZOFURAN-1(3H)-ONE 95.00%
1G
$ 646.80

American Custom Chemicals Corporation
4,5,6,7-TETRACHLOROISOBENZOFURAN-1(3H)-ONE 95.00%
0.5G
$ 605.00

AHH
Fthalide 98%
10g
$ 730.00

Total 28 raw suppliers

Chemical Property of 4,5,6,7-Tetrachlorophthalide

Chemical Property:

Appearance/Colour:white to light yellow crystal powder
Vapor Pressure:8.38E-09mmHg at 25°C
Melting Point:209-210oC
Refractive Index:1.5282 (estimate)
Boiling Point:464.4°Cat760mmHg
Flash Point:215.8°C
PSA：26.30000
Density:1.767g/cm³
LogP:3.97060
Storage Temp.:0-6°C
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:271.877940
Heavy Atom Count:14
Complexity:260

Purity/Quality:

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

Phthalide(Fthalide) ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2=C(C(=C(C(=C2Cl)Cl)Cl)Cl)C(=O)O1
Uses Phthalide (Fthalide) is a fungicide used against the Penicillium and Aspergiillus species of fungus. Pesticide.

Technology Process of 4,5,6,7-Tetrachlorophthalide

There total 10 articles about 4,5,6,7-Tetrachlorophthalide 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: 86.0%

: 117-08-8
tetrachlorophthalic anhydride

: 27355-22-2
4,5,6,7-tetrachloroisobenzofuran-1(3H)-one

Guidance literature:: With lithium borohydride; In tetrahydrofuran; for 0.25h;

Reference yield: 65.0%

: 56135-96-7
3,4,5,6-tetrachloro-1,2-bis(hydroxymethyl)benzene

: 27355-22-2
4,5,6,7-tetrachloroisobenzofuran-1(3H)-one

: 1579147-86-6
4,5,6,7-tetrachloro-1,3-dihydroisobenzofuran-1-ol

Guidance literature:: With Oxone; 2-iodo-3,4,5,6-tetramethylbenzoic acid; In water; acetonitrile; at 30 ℃; for 24h; Green chemistry;
DOI:10.1016/j.tet.2014.01.034