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Benzeneselenol, thallium(1+) salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72017-00-6

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72017-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72017-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,1 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72017-00:
(7*7)+(6*2)+(5*0)+(4*1)+(3*7)+(2*0)+(1*0)=86
86 % 10 = 6
So 72017-00-6 is a valid CAS Registry Number.

72017-00-6SDS

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 Thallous Phenyl Selenide

1.2 Other means of identification

Product number -
Other names Thallous phenylselenide

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:72017-00-6 SDS

72017-00-6Relevant academic research and scientific papers

The direct electrochemical synthesis of phenylselenolato complexes of some main group and late transition elements

Kumar, Rajesh,Tuck, Dennis G.

, p. 127 - 129 (2007/10/02)

The electrochemical oxidation of anodes of selected Main Group or late transition metals (M) in non-aqueous solutions of diphenyl diselenide gives the corresponding M(SePh)n compounds in high yields (M=Zn, Cd, n=2; M=Cu, Ag, Tl, n=1; M=Sn, n=4)

Reactions of Some Main Group Metals with Diphenyl Disulphide and Diphenyl Diselenide

Kumar, Rajesh,Mabrouk, Hassan E.,Tuck, Dennis G.

, p. 1045 - 1048 (2007/10/02)

Indium reacts with both Ph2S2 and Ph2Se2 in refluxing toluene to give the compounds In(EPh)3 (E = S or Se) in high yield.Under similar conditions tin gives Sn(EPh)4.Thallium reacts with Ph2Se2 to form Tl(SePh), but does not react with Ph2S2.Neither zinc nor gallium reacts with Ph2S2 or Ph2Se2.With mixtures of Ph2E2 and I2, indium yields the previously unreported InI(EPh)2 compounds.The reactions of In(SePh)3 are those of a typical indium(III) Lewis acid.Possible factors affecting the reactions of metals with Ph2S2 or Ph2Se2 are briefly discussed.

Substitution Reactions of Thallous Thiophenoxide and Thallous Phenylselenide with Halogen-Bearing Substrates

Detty, Michael R.,Wood, Gary P.

, p. 80 - 89 (2007/10/02)

Thallous thiophenoxide (1) and thallous selenide (2) were prepared by the action of either thallous ethoxide or thallous pentoxide on thiophenol and benzeneselenol.The reagents 1 and 2 reacted readily with aroyl and acyl halides, imidoyl chlorides, α-halo ketones, α-halo esters, α-halo lactones, α-halo carboxylic acids, allyl halides, alkyl halides, chlorotrimethylsilane, chloroacetonitrile, and N-chlorosuccinimide to give substitution products and varying amounts of diphenyl disulfide and diphenyl diselenide.The reactions were run as heterogeneous mixtures in ether.The origin of the diphenyl disulfide and diphenyl diselenide was homolytic cleavage of the thallium-sulfur or thallium-selenium bond, on the basis of the products derived from the reactions of N-chlorosuccinimide with 1 and 2.

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