1506-15-6 Usage
Uses
Used in Pesticide Industry:
1,2,3,4,5,6-Hexachloro-7-methoxynaphthalene, tech. is used as a pesticide for its strong insecticidal properties, providing effective control over various pests that can damage crops and other plants. Its application in this industry is aimed at protecting agricultural yields and maintaining the health of plant life.
Used in Insecticide Applications:
In the insecticide sector, 1,2,3,4,5,6-hexachloro-7-methoxynaphthalene, tech. serves as a potent agent for eliminating insects that can transmit diseases or cause structural damage. Its use is particularly valuable in areas where insect-borne illnesses are a concern, as well as in construction and wood preservation to prevent infestations and decay.
Environmental Considerations:
Given the chemical's high toxicity to aquatic organisms and potential for long-term environmental harm, it is crucial to handle and dispose of 1,2,3,4,5,6-hexachloro-7-methoxynaphthalene, tech. with extreme care. Strict adherence to regulations is necessary to minimize its impact on ecosystems and to ensure the safety of both wildlife and human populations.
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 academic research and scientific papers
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.
