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1043-50-1

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1043-50-1 Usage

General Description

Pentafluorophenyl sulfide is a chemical compound with the formula C6F5S. It is a colorless to light yellow liquid with a pungent odor. Pentafluorophenyl sulfide is used as a reagent in organic synthesis and in the production of pharmaceuticals, agrochemicals, and materials science. It reacts with various nucleophiles and electrophiles to form new carbon-sulfur bonds, making it a valuable building block in organic chemistry. Additionally, it is a useful precursor for the preparation of other sulfur-containing compounds, and has potential applications in the development of new materials with specific properties. Pentafluorophenyl sulfide is also utilized as a ligand in coordination chemistry and as a stabilizing agent for various metal nanoparticles. While it has low acute toxicity, proper safety precautions should be taken when handling and working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1043-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1043-50:
(6*1)+(5*0)+(4*4)+(3*3)+(2*5)+(1*0)=41
41 % 10 = 1
So 1043-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C12F10S/c13-1-3(15)7(19)11(8(20)4(1)16)23-12-9(21)5(17)2(14)6(18)10(12)22

1043-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Pentafluorophenyl sulfide

1.2 Other means of identification

Product number -
Other names 1,2,3,4,5-pentafluoro-6-(2,3,4,5,6-pentafluorophenyl)sulfanylbenzene

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:1043-50-1 SDS

1043-50-1Relevant articles and documents

Chambers,Cunningham

, p. 469 (1966)

-

Deacon,Parrott

, p. P17 (1969)

-

-

Cohen et al.

, p. 451 (1967)

-

Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+

Makarov, Alexander Yu.,Bagryanskaya, Irina Yu.,Zhivonitko, Vladimir V.

, (2020)

[Figure not available: see fulltext.] Reactions of 1,3λ4δ2,2,4-benzothiadiazines with SCl2, C6F5SCl, and [NS2][SbF6] leading to 1,2,3-benzodithiazolium salts (Herz salts) were in

-

Clark, R. J. H.,Kaminaris, D.

, p. L7 - L8 (1974)

-

Convenient Synthesis of Symmetrical Polyfluorinated Diphenyl Sulfides

Bredikhin, R. A.,Maksimov, A. M.,Nikul’shin, P. V.,Platonov, V. E.

, p. 1921 - 1930 (2022/01/24)

Abstract: Thermal properties of decafluorodiphenyl disulfide in the pure state and in the presence of copper and iron metals have been studied. A procedure has been proposed for the synthesis of symmetrical poly-fluorinated diaryl sulfides from diaryl dis

HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXVII. REACTIONS OF ALKANETHIONES WITH THE CHLORINE DERIVATIVES OF BENZENE, THIOPHENE, AND NAPHTHALENE

Voronkov, M. G.,Deryagina, E. N.,Sukhomazova, E. N.

, p. 755 - 760 (2007/10/02)

Alkanethiols react effectively with chlorobenzene, its derivatives, 1-chloronaphthalene, and 2-chlorothiophene at 600-660 deg C with the preferential formation of the corresponding aromatic or heteroatomic thiols.Ethanethiol is most reactive.When it is used instead of hydrogen sulfide in reactions with chlorobenzene or its 4-substituted derivatives, the yield of the aromatic thiols, from which the phenylthiyl radicals are generated with greater difficulty, increases more sharply than the yield of the thiophenols, which generate the more stable 4-XC6H4S radicals.The side products of the reactions are the corresponding diaryl sulfides, thiophene, benzothiophene, and toluene.

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