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2,4,6-triphenylbenzenethiol is a chemical compound with the molecular formula C18H14S. It is a thiol, meaning it contains a sulfur atom bonded to a hydrogen atom, and has three phenyl (C6H5) groups attached to the benzene ring. 2,4,6-triphenylbenzenethiol is known for its aromatic odor and is commonly used in organic synthesis and as a building block for creating more complex molecules.

4435-66-9

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4435-66-9 Usage

Uses

Used in Organic Synthesis:
2,4,6-triphenylbenzenethiol is used as a building block for [creating more complex molecules] because of [its unique structure and properties].
Used in Perfume and Fragrance Industry:
2,4,6-triphenylbenzenethiol is used as a fragrance ingredient for [its aromatic odor], contributing to [the creation of various perfumes and fragrances].
Used in Coating Industry:
2,4,6-triphenylbenzenethiol is used as a corrosion inhibitor for [protecting materials from corrosion], enhancing the durability and longevity of coated surfaces.
Used in Plastics and Rubber Industry:
2,4,6-triphenylbenzenethiol is used as a stabilizer for [plastic and rubber products] to [improve their stability and resistance to degradation].

Check Digit Verification of cas no

The CAS Registry Mumber 4435-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4435-66:
(6*4)+(5*4)+(4*3)+(3*5)+(2*6)+(1*6)=89
89 % 10 = 9
So 4435-66-9 is a valid CAS Registry Number.

4435-66-9Upstream product

4435-66-9Relevant academic research and scientific papers

The synthesis and characterization of metal derivatives of the new, conveniently prepared, bulky thiolato ligand HSC6H2-2,4,6-Ph3

Ruhlandt-Senge, K.,Power, P. P.

, p. 594 - 598 (2007/10/02)

The facile synthesis and characterisation of the new bulky thiol HSC6H2-2,4,6-Ph3 (HSTriph), 1, and two of its metal derivatives are described.The thiol was synthesized by the reaction of Li(OEt2)2Triph with sulfur followed by hydrolysis with dilute sulfuric acid.Treatment of HSTriph with n-BuLi afforded the monomeric Li(THF)3STriph, 2, and the reaction of 1 with the iron silylamide, Fe2, yielded the dimer 2, 3.The compounds were characterized by IR spectroscopy and the meetal derivatives by X-ray crystallography.Crystal data with MoKα(λ = 0.71069 Angstroem) at 130 K: 2, a = 9.392(2) Angstroem, b = 11.254(3) Angstroem, c = 15.304(5) Angstroem, α = 97.72(2) deg, β = 94.42(2) deg, γ = 100.93(7) deg, V = 1565.2(7) Angstroem3, Z = 2, space group P1, 3820 (I > 2?(I)) data, R = 0.07; 3, a = 12.035(3) Angstroem, b = 18.328(7) Angstroem, c = 16.505(5) Angstroem, β = 98.90(2) deg, V = 3597(2) Angstroem3, Z = 2, space group P21/n, 2518 (I > 2?(I)) data, R = 0.06. Key words: Transition metal thiolate / triphenylbenzenethiol

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