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9H-10-Selenaanthracen-9-one is a unique organoselenium compound characterized by the presence of a selenium atom in its structure. It belongs to the family of anthracenone derivatives, which are known for their diverse applications in various fields such as pharmaceuticals, materials science, and organic synthesis. The compound features a selenium atom at the 10th position and a carbonyl group at the 9th position of the anthracene core, which significantly influences its chemical properties and reactivity. Due to its distinctive structure, 9H-10-Selenaanthracen-9-one has potential applications in the development of new materials and as a building block for more complex organic molecules.

4734-58-1

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4734-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4734-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4734-58:
(6*4)+(5*7)+(4*3)+(3*4)+(2*5)+(1*8)=101
101 % 10 = 1
So 4734-58-1 is a valid CAS Registry Number.

4734-58-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name selenoxanthen-9-one

1.2 Other means of identification

Product number -
Other names 9H-Selenoxanthen-9-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4734-58-1 SDS

4734-58-1Downstream Products

4734-58-1Relevant academic research and scientific papers

Synthesis of 9-oxoselenoxanthenium and triarylselenonium hexafluorophosphates

Loskutov,Balina,Russkikh,Shelkovnikov

, p. 1093 - 1097 (2015/06/30)

The selenoxides forming 9-oxoselenoxanthenium and triaryl selenonium hexafluorophosphates via interaction with heptyl phenyl ether and anisole in the MeSO3H-P2O5 mixture followed by treatment with KPF6 have been obtained via selenoxantene-9-one and diphenyl selenide derivatives oxidation with m-chloroperoxybenzoic acid or hydrogen peroxide.

Synthesis, Stereochemistry and Reactions of Selenoxanthen-10-io(alkoxalyl alkoxycarbonyl)methanides and Related Compounds

Kataoka, Tadashi,Tomimatsu, Kiminori,Shimizu, Hiroshi,Hori, Mikio

, p. 2666 - 2675 (2007/10/02)

Selenoxanthen 10-oxides (5a-d) reacted with methyl propiolate, dimethyl and diethyl acetylenedicarboxylates to afford selenoxanthen-10-iometanides (6a-i).The 9-isopropyl derivative gave only trans-ylides and the 9-phenyl congener formed cis- and trans-ylides.The stereochemistry is discussed on the basis of the nuclear magnetic resonance spectral data.Reduction of the selenoxanthenium ylides with sodium borohydride afforded the ylide lactones (16a-c) and the ylide alcohols (17a-f).The Product ratio depended on the solvent used.Keywords - selenium ylide; selenoxide; selenoxanthene; methyl propiolate; dimethyl acetylenedicarboxylate; stereoisomer; stereochemistry; sodium borohydride reduction; lactonization

NOVEL REDUCTION OF CHLORINE ADDUCTS OF ARYL AND ALKYL SELENIDES WITH DIMETHYL SULFOXIDE

Nakanishi, Waro,Sakaue, Akira,Ikeda, Yoshitsugu,Iwamura, Hiizu

, p. 33 - 34 (2007/10/02)

The adducts of chlorine with diaryl selenides such as selenanthrene, diphenyl selenide, and selenoxanthone have been found to be reduced to the corresponding selenides in dimethyl sulfoxide forming chloromethyl methyl sulfoxide and hydrogen chloride.Similarly, dimethyl selenide dichloride was reduced to dimethyl selenide in the presence of a base.

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