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trans-2,4-diphenylthietane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24609-87-8

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24609-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24609-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24609-87:
(7*2)+(6*4)+(5*6)+(4*0)+(3*9)+(2*8)+(1*7)=118
118 % 10 = 8
So 24609-87-8 is a valid CAS Registry Number.

24609-87-8Downstream Products

24609-87-8Relevant academic research and scientific papers

Carbon-sulfur bond cleavage with a loss of stereochemistry in the ring opening of trans-2,4-diphenylthietane by Os3(CO)10(NCMe)2

Adams, Richard D.,Pompeo, Michael P.

, p. 103 - 111 (2008/10/08)

The reaction of Os3(CO)10(NCMe)2 with trans-2,4-diphenylthietane (2,4-DPT) at 25 °C resulted in the formation of two isomers, cis- and trans-Os3(CO)10[μ-SC(H)PhCH2C(H)Ph] (1), in a combined yield of 76%. The cis product was characterized by single-crystal X-ray diffraction analysis and was found to contain a thiametalladiphenylcyclopentane ring formed by the opening of the thietane ring. The cis and trans isomers differ in the orientation of their phenyl substituents. The isomers are formed in approximately equal amounts in the early stages of the reaction, but the trans isomer subsequently slowly isomerizes to the cis isomer. The observed loss in stereochemistry at the carbon center is attributed to a stepwise ring-opening mechanism. When compound 1 was heated to 97 °C under a CO atmosphere, five compounds were formed: Os3(CO)10[μ-SC(H)PhC(H)=C(H)Ph[(μ-H) (2) (22%), Os2(CO)7[μ-SC(H)(C6H4)CH 2CH2Ph] (3) (11%), Os3(CO)11[μ-SC(H)PhCH2C(H)Ph] (4) (39%), H2Os6(CO)17(μ3-S)(μ 4-S) (5) (a trace amount), and Os3(CO)12. Compounds 3 and 5 and the known compound Os3(CO)9(μ3-CO)(μ3-S) (6) were obtained in better yields by heating 2 to 125 °C in octane solvent. Compounds 2-4 were characterized by IR, 1H NMR, and single-crystal X-ray diffraction analyses. Compound 2 is an isomer of 1 and contains a diphenylpropenethiolate and hydride ligand formed by a β-eliminationβ transformation of the ring system in 1. The mechanism of this transformation was not established. Compound 3 contains only two metal atoms and an ortho-metalated phenyl ring. Compound 4 is a CO adduct of 1 formed by the cleavage of the sulfur-bridged metal-metal bond. Crystallographic data are as follows. cis-1: space group P21/c, a = 8.674 (2) A?, b = 35.09 (1) A?, c = 9.449 (2) A?, β = 106.41 (1)°, Z = 4, 2053 reflections, R = 0.033. 2: space group C2/c, a = 13.845 (2) A?, b = 14.545 (4) A? c = 28.907 (6) A?, β = 98.88 (1)°, Z = 8, 2519 reflections, R = 0.027. 3: space group P21/c, a = 8.337 (1) A?, b = 17.311 (4) A?, c = 16.409 (3) A?, β = 100.82 (1)°, Z = 4, 2299 reflections, R = 0.036. 4: space group P1, a = 14.319 (2) A?, b = 17.794 (5) A?, c = 12.257 (4) A?, α = 106.69 (2)°, β = 90.74 (2)°, γ = 82.56 (2)°, Z = 4, 4020 reflections, R = 0.041.

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