2-(Phenylselanyl)prop-2-enal

Base Information

Chemical Name:2-(Phenylselanyl)prop-2-enal
CAS No.:61713-63-1
Molecular Formula:C9H8OSe
Molecular Weight:211.122
Hs Code.:
DSSTox Substance ID:DTXSID40515769
Nikkaji Number:J1.315.401E
Wikidata:Q82376833

Synonyms:2-(Phenylselanyl)prop-2-enal;61713-63-1;DTXSID40515769

Suppliers and Price of 2-(Phenylselanyl)prop-2-enal

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 0 raw suppliers

Chemical Property of 2-(Phenylselanyl)prop-2-enal

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:211.97404
Heavy Atom Count:11
Complexity:148

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=C(C=O)[Se]C1=CC=CC=C1

Technology Process of 2-(Phenylselanyl)prop-2-enal

There total 9 articles about 2-(Phenylselanyl)prop-2-enal 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: 83.0%

: 1666-13-3
diphenyl diselenide

: 107-19-7
propargyl alcohol

: 61713-63-1
α-(phenylseleno)acrolein

Guidance literature:: With Selectfluor; In acetonitrile; at 20 ℃; for 12h;
DOI:10.1021/acs.joc.1c00167

Reference yield:

: 82737-08-4
N-(phenylselanyl)morpholine

: 107-02-8,25068-14-8
acrolein

: 110-91-8,99108-56-2
morpholine

: 61713-63-1
α-(phenylseleno)acrolein

Guidance literature:: With silica gel; Multistep reaction. Yields of byproduct given; 1.) hexane, 20 deg C, 18 h;
DOI:10.1016/S0040-4039(01)90093-0