2717-42-2 Usage
General Description
1,2,4-Trimethylnaphthalene, also known as 1,2,4-TMN, is a chemical compound with the molecular formula C13H12. It is a polycyclic aromatic hydrocarbon (PAH) that consists of a naphthalene ring with three methyl groups attached at positions 1, 2, and 4. 1,2,4-Trimethylnaphthalene is a white crystalline solid with a strong, aromatic odor, and it is insoluble in water but soluble in organic solvents. 1,2,4-TRIMETHYLNAPHTHALENE is commonly used as a fragrance ingredient in the production of perfumes and personal care products. It is also utilized as a chemical intermediate in the synthesis of various pharmaceuticals and pesticides. Additionally, 1,2,4-Trimethylnaphthalene has potential applications in organic light-emitting diodes (OLEDs) and as a heat transfer fluid in high-temperature processes. However, it is important to handle 1,2,4-Trimethylnaphthalene with caution due to its potential to cause skin and eye irritation upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 2717-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2717-42:
(6*2)+(5*7)+(4*1)+(3*7)+(2*4)+(1*2)=82
82 % 10 = 2
So 2717-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14/c1-9-8-10(2)12-6-4-5-7-13(12)11(9)3/h4-8H,1-3H3
2717-42-2Relevant articles and documents
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Aslam,F.M. et al.
, p. 892 - 894 (1972)
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Photooxidation of methylnaphthalenes
Wasserman, Harry H.,Wiberg, Kenneth B.,Larsen, David L.,Parr, Jonathan
, p. 105 - 109 (2007/10/03)
(Chemical Equation Presented). Studies on the photooxidation of methyl-substituted aromatic hydrocarbons have revealed that whereas electron density is a determinant of endoperoxide formation, steric factors are most important in influencing the stability of the endoperoxide. Additional information on the energetics of the reactions and on the magnitude of the steric interactions was obtained using calculations at the B3LYP/6-311+G* level of theory.
Acid induced rearrangement of α,γ-unsaturated ketones
Banerjee, Ajoy K.,Acevedo, Julio C.,Gonzalez, Rosana,Rojas, Anibal
, p. 2081 - 2086 (2007/10/02)
The molecular rearrangement of the ketones (1), (10) and (19) to phenanthrene derivative (3) and decalin derivative (11) and (12) is respectively described.
