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C21H20NSe(1+)*F6P(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135285-79-9

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135285-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135285-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135285-79:
(8*1)+(7*3)+(6*5)+(5*2)+(4*8)+(3*5)+(2*7)+(1*9)=139
139 % 10 = 9
So 135285-79-9 is a valid CAS Registry Number.

135285-79-9Downstream Products

135285-79-9Relevant academic research and scientific papers

Synthesis, crystal structure, and reactivity of new amino- and ammonio- selenuranes containing transannular Se-N bond from 5H,7H- dibenzo[b,g][1,5]selenazocines

Mima, Hisatomo,Fujihara, Hisashi,Furukawa, Naomichi

, p. 743 - 752 (2007/10/03)

The reaction of N-methyl-5H,7H-dibenzo[b,g][1,5]selenazocine Se-oxide 2 with SOCl2 gave the chloroammonioselenurane 3b which was further converted into the methyl- or phenyl- substituted ammonioselenurane (4 or 5) upon treatment with Me2/

A,3-Allylic Strain as a Control Element in the Paterno-Buechi Reaction of Chiral Silyl Enol Ethers: Synthesis of Diastereomerically Pure Oxetanes Containing Four Contiguous Stereogenic Centers

Bach, Thorsten,Joedicke, Kai,Kather, Kristian,Froehlich, Roland

, p. 2437 - 2445 (2007/10/03)

The facial diastereoselectivity in the Paterno-Buechi reaction of chiral enol ethers and benzaldehyde was studied. The substituents (RS, RL) at the stereogenic carbon atom (-C*HRSRL) attached to the β-position o

FORMATION OF DICATION AND HYPERVALENT BOND FROM 5H,7H-DIBENZOSELENAZOCINE

Fujihara, Hisashi,Mima, Hisatomo,Furukawa, Naomichi

, p. 141 - 144 (2007/10/02)

The reaction of the selenoxide 2 of N-methyl-5H,7H-dibenzo-selenazocine (1) with (CF3SO2)2O gave the selenaza dication salt 3 which acts as an oxidizing agent.A novel ?-selenurane 4 was prepared by either the reaction of selenide 1 with t-BuOCl or the reaction of selenoxide 2 with SOCl2; the crystal structure of 4 shows the chloroammonioselenurane with a distorted trigonal-bipyramidal geometry around the selenium atom.

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