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1,3,2-Thiazaphosphole, 2,3-dihydro-2-(4-methoxyphenyl)-3,4,5-triphenyl-, 2-sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82998-36-5

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82998-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82998-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,9 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82998-36:
(7*8)+(6*2)+(5*9)+(4*9)+(3*8)+(2*3)+(1*6)=185
185 % 10 = 5
So 82998-36-5 is a valid CAS Registry Number.

82998-36-5Downstream Products

82998-36-5Relevant academic research and scientific papers

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS PART VIII. THE ACTION OF 1,3,2,4-DITHIADIPHOSPHETANE-2,4-DISULFIDES ON BENZILMONOANILS. NOVEL SYNTHESIS OF 4,5-DIPHENYL Δ4-1,3,2-THIAZAPHOSPHOLINE-2-SULFIDE DERIVATIVES

Shabana, R.,Mahran, M. R.,Hafez, T. S.

, p. 1 - 6 (2007/10/02)

1,3,2,4-Dithiadiphosphetane 2,4-disulfides 1a,b react with benzilmonoanils 2a-d to give 4,5-diphenyl Δ4-1,3,2-thiazaphospholine-2-sulfide derivatives of type 3.Compatible analytical and spectroscopic results were obtained for all the new compou

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS-XL. REACTIONS OF KETONES WITH 2,4-BIS(4-METHOXYPHENYL)-1,3,2,4-DITHIADIPHOSPHETANE 2,4-DISULFIDE

Scheibye, S.,Shabana, R.,Lawesson, S.-O.,Romming, C.

, p. 993 - 1002 (2007/10/02)

Cyclohexanone and cyclopentanone react with (2,4-bis-4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (Lawesson Reagent (LR)) at 80 deg C with formation of new spiro-1,3,5,2-trithiaphosphorines 1 and 2, respectively. 2-Methyl and 2-phenylcyclohexanone also react with LR at 80 deg C producing the enethiols 3 and 4, which on storage are transformed into the sulfides 5 and 6.Unsaturated cyclohexanones 7-9 are transformed into the corresponding thioketones 10-12 after reactions with LR at 60 deg C for a few hours. 2-Hydroxyketones react with LR with formation of 1,3,2-oxathiaphospholes and similarly a 2-aminoketone gave a 1,3,2-thiazaphosphole.Aromatic ketones, reacted with LR to give corresponding thioketones.Thiofluorenone dimerized to form the cyclic disulfide 31, as proved by X-ray analyses.

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