DIBENZYL SELENIDE

Base Information

• Chemical Name: DIBENZYL SELENIDE
• CAS No.: 1842-38-2
• Molecular Formula: C14H14 Se
• Molecular Weight: 261.225
• Hs Code.: 2931900090
• NSC Number: 168575
• DSSTox Substance ID: DTXSID00171547
• Nikkaji Number: J104.997F
• Wikidata: Q83041632
• Mol file: 1842-38-2.mol

Synonyms:Benzylselenide (6CI,7CI,8CI); Bis(phenylmethyl)selenide; Dibenzyl monoselenide;Dibenzyl selenide; NSC 168575

Chemical Property of DIBENZYL SELENIDE

Chemical Property:

• Vapor Pressure: 4.06E-05mmHg at 25°C
• Boiling Point: 362.3°Cat760mmHg
• Flash Point: 172.9°C
• PSA: 0.00000
• Density: g/cm³
• LogP: 3.62380
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 4
• Exact Mass: 262.02607
• Heavy Atom Count: 15
• Complexity: 137

Purity/Quality:

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

BENZYL SELENIDE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C[Se]CC2=CC=CC=C2

Technology Process of DIBENZYL SELENIDE

There total 50 articles about DIBENZYL SELENIDE 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: 99.0%

N-(phenylsulfonyl)dibenzylselenimide (71150-57-7) + phenylmethanethiol (100-53-8) → benzenesulfonamide (98-10-2) + dibenzyl disulphide (150-60-7) + dibenzyl selenide (1842-38-2)

Guidance literature:

In chloroform; for 0.333333h; Product distribution; Ambient temperature;

Reference yield: 98.0%

N-(p-tolylsulfonyl)dibenzylselenimide (55986-20-4) + phenylmethanethiol (100-53-8) → dibenzyl disulphide (150-60-7) + dibenzyl selenide (1842-38-2) + toluene-4-sulfonamide (70-55-3)

Guidance literature:

In chloroform; for 0.333333h; Product distribution; Ambient temperature;

Reference yield: 98.0%

dibenzyl diselenide (1482-82-2) + N-benzyl-2,4,6-triphenylpyridinium tetrafluoroborate (66310-10-9) → dibenzyl selenide (1842-38-2)

Guidance literature:

With eosin Y disodium salt; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 20h; Schlenk technique; Inert atmosphere; Irradiation; Green chemistry;

DOI:10.1016/j.tetlet.2021.153071

upstream raw materials:

dibenzyl diselenide

benzyldimethylphenylammonium chloride

benzyl chloride

benzyl selenocyanate

Downstream raw materials:

dibenzyl selenoxide

benzyl seleninic acid

benzyl methyl ether

dibenzyl diselenide