1506-15-6 Usage
General Description
The chemical 1,2,3,4,5,6-hexachloro-7-methoxynaphthalene, tech. is a synthetic compound that is primarily used as a pesticide and insecticide. It is a member of the naphthalene family of chemicals, which are known for their strong insecticidal properties. This particular compound is highly toxic to aquatic organisms and may cause long-term adverse effects in the environment. It is also listed as a hazardous substance in the United States and is subject to strict regulations for its use and disposal. Due to its toxicity and potential for environmental harm, careful handling and proper disposal of this chemical is necessary to minimize its impact on the ecosystem.
Check Digit Verification of cas no
The CAS Registry Mumber 1506-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1506-15:
(6*1)+(5*5)+(4*0)+(3*6)+(2*1)+(1*5)=56
56 % 10 = 6
So 1506-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H4Cl6O/c1-18-4-2-3-5(8(14)7(4)13)9(15)11(17)10(16)6(3)12/h2H,1H3
1506-15-6Relevant articles and documents
Identification of hydroxylated chlorodibenzo-p-dioxins, chlorodibenzofurans, chlorodiphenyl ethers and chloronaphthalenes as their methyl ethers by gas chromatography mass spectrometry
Tulp Th.,Hutzinger
, p. 224 - 231 (2007/10/05)
The methyl ethers of a number of hydroxylated (poly)chlorodibenzo-p-dioxins, chlorodibenzofurans, chlorodiphenyl ethers and chloronaphthalenes, representing all different hydroxy substitutions, were synthesized and their mass spectra investigated. With the exception of the methoxy derivatives of the chlorodibenzofurans, it appeared that the mass fragmentation patterns of the structural isomers of each class of compounds were very specific and allowed unambiguous assignment of the position of the methoxy group in the molecule. The different fragmentation patterns can be explained in terms of plausible mechanisms resulting in stable charge delocalized (oxonium) ions. Because of its diagnostic value, this method is useful in the structure elucidation of hydroxylated metabolites of pure isomers of chlorodibenzo-p-dioxins, chlorodiphenyl ethers and chloronaphthalenes.
