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3,5-di-p-fluorophenyl-2,4,6-trimethyl-cyclo-1-oxa-3,5-diaza-2,4,6-triborane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84790-08-9

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84790-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84790-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,9 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84790-08:
(7*8)+(6*4)+(5*7)+(4*9)+(3*0)+(2*0)+(1*8)=159
159 % 10 = 9
So 84790-08-9 is a valid CAS Registry Number.

84790-08-9Downstream Products

84790-08-9Relevant academic research and scientific papers

Reactions of N-Sulfinyl Compounds with the 1,2,4-Trithia-3,5-diborolane Ring System and Substitution Reaktionens at the 1,2,4-Trithia-3,5-diborolane and 1,2-Dithia-4-aza-3,5-diborolidine Systems

Meller, Anton,Habben, Carl

, p. 139 - 154 (2007/10/02)

The reaction of trimethylsilyl- and pentafluorophenyl-N-sulfinylamine respectively with 3,5-dihalogeno-1,2,4-trithia-3,5-diborolanes yields the 1,2-dithia-4-aza-3,5-diborolidines 1-3.Tert-butyl-N-sulfinylamine and 3,5-dimethyl-1,2,4-trithia-3,5-diborolane react analogous.Other N-sulfinylamines however split the disulfane bridge in 3,5-dimethyl-1,2,4-trithia-3,5-diborolane and the 1,4-dithia-2-aza-3,5-diborolidines 5(A)-7(A) are formed.Besides of boroxines, cyclo-2,4,6-trimethyl-1,3-dioxa-5-aza-2,4,6-triboranes and cyclo-2,4,6-trimethyl-1-oxa-3,5-diaza-2,4,6-triboranes are formed as byproducts, 8-10 have been isolated.In 1,2,4-trithia-3,5-diborolanes and 1,2-dithia-4-aza-3,5-diborolidines the bromo-atoms can be substituted by alkyl (13, 14), by amino (15-21) and by isothiocyanato groups.The compounds were characterised analytically and spectroscopycally (MS; NMR: 1H, 11B, 19F, 29Si; IR).Keywords: Boroxazines; 1,2-Dithia-4-aza-3,5-diborolidines; 1,4-Dithia-2-aza-3,5-diborolidines; N-Sulfonylcompounds; 1,2,4-Trithia-3,5-diborolane.

Crystal and Molecular Structure of 5-p-Fluorophenyl-2,4,6-trimethylcyclo-1,3-dioxa-2,4,6-triborane

Meller, Anton,Habben, Carl,Noltemeyer, Mathias,Sheldrick, George M.

, p. 1504 - 1506 (2007/10/02)

The title compound, isolated from the reaction of p-fluorophenyl-N-sulphinylamine with 3,5-dimethyl-1,2,4-trithia-3,5-diborolane, crystallizes in the orthorhombic space group Pnma with a = 736.2(2), b = 1256.6(2), c = 1330.6(2) pm and Z = 4.The heterocyclic ring lies in a crystallographic mirror plane, with the para-fluorophenyl substituent at right angles to the plane. - Key words: Crystal Structure, Synthesis, Borazoxine

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