(Benzenesulfonyl)(phenyl)methanone

Base Information

Chemical Name:(Benzenesulfonyl)(phenyl)methanone
CAS No.:72818-29-2
Molecular Formula:C13H10O3S
Molecular Weight:246.287
Hs Code.:
DSSTox Substance ID:DTXSID30502380
Wikidata:Q82355345

Synonyms:(Benzenesulfonyl)(phenyl)methanone;72818-29-2;SCHEMBL5187614;DTXSID30502380

Suppliers and Price of (Benzenesulfonyl)(phenyl)methanone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (Benzenesulfonyl)(phenyl)methanone

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:246.03506535
Heavy Atom Count:17
Complexity:355

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of (Benzenesulfonyl)(phenyl)methanone

There total 7 articles about (Benzenesulfonyl)(phenyl)methanone 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:

: 186422-70-8
phenyl phenylsulfonyl ketone O-oxide

: 72818-29-2
phenyl phenylsulfonyl ketone

Guidance literature:: In gaseous matrix; at -263.2 ℃; Irradiation;
DOI:10.1021/ja962949k

Reference yield:

: 61937-46-0
2-phenyl-1-(phenylsulfonyl)-1,2-epoxyethane

: 72818-29-2
phenyl phenylsulfonyl ketone

Guidance literature:: Multi-step reaction with 5 steps

1: 26 percent / BF₃*Et₂O / CH₂Cl₂ / 0.17 h / 0 °C

2: 21 percent / HOOC-C₆H₄-SO₂N₃, aq. NH₃ / CH₂Cl₂ / 20 h / Ambient temperature

3: gaseous matrix / -263.2 °C / Irradiation

4: O₂ / gaseous matrix / -232.2 °C

5: gaseous matrix / -263.2 °C / Irradiation

With ammonium hydroxide; HOOC-C₆H₄-SO₂N₃; boron trifluoride diethyl etherate; oxygen; In dichloromethane;
DOI:10.1021/ja962949k

Reference yield:

: 7205-98-3
chloromethyl phenyl sulfone

: 72818-29-2
phenyl phenylsulfonyl ketone

Guidance literature:: Multi-step reaction with 6 steps

1: 67 percent / aq. NaOH, benzyltriethylammonium chloride / acetonitrile / 1.5 h / 0 °C

2: 26 percent / BF₃*Et₂O / CH₂Cl₂ / 0.17 h / 0 °C

3: 21 percent / HOOC-C₆H₄-SO₂N₃, aq. NH₃ / CH₂Cl₂ / 20 h / Ambient temperature

4: gaseous matrix / -263.2 °C / Irradiation

5: O₂ / gaseous matrix / -232.2 °C

6: gaseous matrix / -263.2 °C / Irradiation

With ammonium hydroxide; sodium hydroxide; HOOC-C₆H₄-SO₂N₃; boron trifluoride diethyl etherate; N-benzyl-N,N,N-triethylammonium chloride; oxygen; In dichloromethane; acetonitrile;
DOI:10.1021/ja962949k