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4,13-bis(p-tolylsulphonyl)-7,10,19,22,27,30-hexaoxa-1,4,13,16-tetra-aza<14.8.8>dotriacontane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113917-92-3

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113917-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113917-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 113917-92:
(8*1)+(7*1)+(6*3)+(5*9)+(4*1)+(3*7)+(2*9)+(1*2)=123
123 % 10 = 3
So 113917-92-3 is a valid CAS Registry Number.

113917-92-3Downstream Products

113917-92-3Relevant 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.

Macroheterocycles; XXXIX. A Convenient Synthesis of Polyaza-oxa Cryptands

Lukyanenko, N. G.,Basok, S. S.,Filonova, L. K.

, p. 335 - 336 (2007/10/02)

A convenient procedure is proposed for the synthesis of cryptands by the alkylation of bis-N-(2-tosylaminoethyl)diaza-crown ethers with dibromides in the two-phase system: aqueous sodium hydroxide/toluene.

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