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4,10-bis(p-tolylsulphonyl)-7,16,19,24,27-pentaoxa-1,4,10,13-tetra-azabicyclo<11.8.8>nonacosane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111306-32-2

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111306-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111306-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,0 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111306-32:
(8*1)+(7*1)+(6*1)+(5*3)+(4*0)+(3*6)+(2*3)+(1*2)=62
62 % 10 = 2
So 111306-32-2 is a valid CAS Registry Number.

111306-32-2Downstream Products

111306-32-2Relevant 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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