1-Propanone, 3-hydroxy-1,3,3-triphenyl-

Base Information

Chemical Name:1-Propanone, 3-hydroxy-1,3,3-triphenyl-
CAS No.:6624-02-8
Molecular Formula:C21H18 O2
Molecular Weight:302.373
Hs Code.:2914400090
NSC Number:55216
DSSTox Substance ID:DTXSID50216437
Wikidata:Q83092668
Mol file:6624-02-8.mol

Synonyms:1-Propanone, 3-hydroxy-1,3,3-triphenyl-;6624-02-8;NSC55216;DTXSID50216437;NSC 55216;NSC-55216

Suppliers and Price of 1-Propanone, 3-hydroxy-1,3,3-triphenyl-

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 4 raw suppliers

Chemical Property of 1-Propanone, 3-hydroxy-1,3,3-triphenyl-

Chemical Property:

Vapor Pressure:6.17E-11mmHg at 25°C
Boiling Point:502.9°C at 760 mmHg
Flash Point:213.1°C
PSA：37.30000
Density:1.164g/cm³
LogP:4.19550
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:302.130679813
Heavy Atom Count:23
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1-Propanone, 3-hydroxy-1,3,3-triphenyl-

There total 19 articles about 1-Propanone, 3-hydroxy-1,3,3-triphenyl- 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: 92.0%

: 120-46-7,61346-73-4
1,3-diphenylpropanedione

: 100-58-3
phenylmagnesium bromide

: 6624-02-8
3-hydroxy-1,3,3-triphenyl-propan-1-one

Guidance literature:: 1,3-diphenylpropanedione; With isopropylmagnesium chloride; In tetrahydrofuran; at 0 ℃; for 0.5h; Inert atmosphere;

phenylmagnesium bromide; In tetrahydrofuran; at 40 ℃; for 4h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c5ob02072g

Reference yield: 70.0%

: 76283-96-0
1,1-Diphenyl-2-(2-phenyl-[1,3]dithian-2-yl)-ethanol

: 6624-02-8
3-hydroxy-1,3,3-triphenyl-propan-1-one

Guidance literature:: With boron trifluoride diethyl etherate; mercury(II) oxide; In tetrahydrofuran; water; Ambient temperature;
DOI:10.1055/s-1980-29122