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4,9-bis(p-tolylsulphonyl)benz-15,20-dioxa-1,4,9,12-tetra-azabicyclo<10.5.5>docosane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121031-84-3

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121031-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121031-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,3 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121031-84:
(8*1)+(7*2)+(6*1)+(5*0)+(4*3)+(3*1)+(2*8)+(1*4)=63
63 % 10 = 3
So 121031-84-3 is a valid CAS Registry Number.

121031-84-3Downstream Products

121031-84-3Relevant academic research and scientific papers

MACROHETEROCYCLES XLVIII. SYNTHESIS OF POLYAZAOXACRYPTANDS IN A TWO-PHASE SYSTEM

Luk'yanenko, N. G.,Basok, S. S.,Filonova, L. K.,Kulikov, N. V.

, p. 1537 - 1544 (2007/10/02)

A method is proposed for the production of polyazaoxacryptands by the condensation of N,N'-bis(tosylaminoethyl)diazacrown ethers with ditosyloxy derivatives or dibromides in the toluene-45percent aqueous sodium hydroxide two-phase system.The catalytic act

MACROHETEROCYCLES. PART 44. FACILE SYNTHESIS OF AZACROWN ETHERS AND CRYPTANDS IN A TWO-PHASE SYSTEM

Lukyanenko, Nikolai G.,Basok, Stepan S.,Filonova, Lyubov K.

, p. 3141 - 3148 (2007/10/02)

A facile procedure is proposed for the preparation of azacrown ethers and cryptands by condensation of dibromides or ethylene glycol bis(toluene-p-sulphonate)s with acyclic bis(sulphonamide)s or with bisdiazacrown ethers, respectively.The reaction was carried out in a two-phase system of aqueous alkali-toluene (benzene)in the presence of quaternary ammonium salts as phase transfer catalysts.The catalytic activity decreased in the sequence: Bu4NI ca.Bu4NBr > Bu4NCl > Bu4NHSO4 > Et3NCH2C6H5NCl.Maximum yields of twelve-membered azacrown ethers are obtained when lithium hydroxide is used, while crown ethers of larger size are observed in the presence of sodium or potassium hydroxides; this may be due to a template effect.

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