[5-Chloro-2-(phenylselanyl)phenyl](phenyl)methanone

Base Information

• Chemical Name: [5-Chloro-2-(phenylselanyl)phenyl](phenyl)methanone
• CAS No.: 88048-89-9
• Molecular Formula: C19H13ClOSe
• Molecular Weight: 371.725
• DSSTox Substance ID: DTXSID50525536
• Wikidata: Q82393210
• Mol file: 88048-89-9.mol

Synonyms:88048-89-9;[5-Chloro-2-(phenylselanyl)phenyl](phenyl)methanone;DTXSID50525536

Chemical Property of [5-Chloro-2-(phenylselanyl)phenyl](phenyl)methanone

Chemical Property:

• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 371.98201
• Heavy Atom Count: 22
• Complexity: 360

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)Cl)[Se]C3=CC=CC=C3

Technology Process of [5-Chloro-2-(phenylselanyl)phenyl](phenyl)methanone

There total 1 articles about [5-Chloro-2-(phenylselanyl)phenyl](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: 93.7%

(2,5-dichlorophenyl)(phenyl)methanone (16611-67-9) + sodium phenylselenide (23974-72-3) → 5-chloro-2-phenylselenobenzophenone (88048-89-9)

Guidance literature:

In N,N-dimethyl-formamide; for 3h; Heating;

Reference yield: 98.0%

5-chloro-2-phenylselenobenzophenone (88048-89-9) → (5-chloro-2-phenylseleno)phenylphenylmethanol (88048-90-2)

Guidance literature:

With sodium tetrahydroborate; In methanol; for 0.5h; Heating;

Reference yield:

5-chloro-2-phenylselenobenzophenone (88048-89-9) → 2-chloro-9-phenylselenoxanthene (88048-91-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 98 percent / NaBH₄ / methanol / 0.5 h / Heating

2: 55.2 percent / 80percent H₂SO₄ / 0.5 h / 95 - 98 °C

With sodium tetrahydroborate; sulfuric acid; In methanol;

upstream raw materials:

(2,5-dichlorophenyl)(phenyl)methanone

sodium phenylselenide

Downstream raw materials:

(5-chloro-2-phenylseleno)phenylphenylmethanol

2-chloro-9-phenylselenoxanthene

N-[2-Chloro-9-phenyl-9H-10λ⁴-selenoxanthen-(10E)-ylidene]-benzenesulfonamide