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9,9'-Bishydroxymethylnaphthalene is an organic compound with the chemical formula C12H12O2. It is a white crystalline solid that is derived from naphthalene, a polycyclic aromatic hydrocarbon. 9,9'-bishydroxymethylnaphthalene is characterized by the presence of two hydroxymethyl groups (-CH2OH) attached to the 9th carbon atoms of the naphthalene molecule. It is used as an intermediate in the synthesis of various chemicals, including polymers and pharmaceuticals, due to its ability to form esters and ethers. The compound is also known for its potential applications in the production of flame retardants and as a precursor in the synthesis of chelating agents. Its chemical properties make it a versatile building block in organic chemistry, although it should be handled with care due to its potential health and environmental impacts.

743-67-9

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743-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 743-67-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,4 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 743-67:
(5*7)+(4*4)+(3*3)+(2*6)+(1*7)=79
79 % 10 = 9
So 743-67-9 is a valid CAS Registry Number.

743-67-9Downstream Products

743-67-9Relevant academic research and scientific papers

THERMAL DISSOCIATION OF DI(ALKYLBENZYL)NAPHTHYL>PEROXYDICARBONATES IN RELATION TO THE STRUCTURE OF THE ALKYL AROMATIC FRAGMENTS

Fomin, V. A.,Etlis, I. V.,Kurskii, Yu. A.,Nozrina, F. D.,Chervyakova, G. N.,Shmuilovich, S. M.

, p. 811 - 819 (2007/10/02)

The kinetics of the thermolysis of di peroxydicarbonates at 40-70 deg C in organic solvents were investigated, the effectiveness of escape of the free radicals from the solvent "cage" was studied, and the final products from thermal dissociation of the peroxydicarbonates were investigated.A scheme was formulated for the thermolysis of peroxides, explaining the relation between the homolysis rate of the O-O group and the reactivity of the obtained free radicals in relation to the structure of the alkylbenzyl fragments in the symmetrical and unsymmetrical peroxydicarbonates.

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