3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline

Base Information

Chemical Name:3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline
CAS No.:128350-90-3
Molecular Formula:C₁₀H₈F₃NO₂
Molecular Weight:231.174
Hs Code.:2933790090
DSSTox Substance ID:DTXSID30561134
Mol file:128350-90-3.mol

Synonyms:128350-90-3;3-HYDROXY-2-OXO-3-TRIFLUOROMETHYL-7-METHYLINDOLINE;3-Hydroxy-7-methyl-3-(trifluoromethyl)indolin-2-one;3-hydroxy-7-methyl-3-(trifluoromethyl)-1H-indol-2-one;DTXSID30561134;3-Hydroxy-7-methyl-3-(trifluoromethyl)-1,3-dihydro-2H-indol-2-one;AKOS017343910;A805810

Suppliers and Price of 3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline

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
3-HYDROXY-2-OXO-3-TRIFLUOROMETHYL-7-METHYLINDOLINE 95.00%
5G
$ 2249.24

AHH
3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline 98%
5g
$ 928.00

Total 6 raw suppliers

Chemical Property of 3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline

Chemical Property:

Vapor Pressure:1.62E-05mmHg at 25°C
Melting Point:125-126 °C(Solv: benzene (71-43-2))
Boiling Point:350.6°C at 760 mmHg
PKA:9.76±0.20(Predicted)
Flash Point:165.9°C
PSA：49.33000
Density:1.483g/cm³
LogP:1.83500
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:0
Exact Mass:231.05071298
Heavy Atom Count:16
Complexity:318

Purity/Quality:

97% ^*data from raw suppliers

3-HYDROXY-2-OXO-3-TRIFLUOROMETHYL-7-METHYLINDOLINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C2C(=CC=C1)C(C(=O)N2)(C(F)(F)F)O

Technology Process of 3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline

There total 1 articles about 3-Hydroxy-2-oxo-3-trifluoromethyl-7-methylindoline 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: 89.0%