2131-42-2 Usage
Uses
Used in Chemical Production:
1,4,6-Trimethylnaphthalene is used as a precursor for the production of various chemical compounds, leveraging its structural properties to facilitate the creation of a range of different substances.
Used in Heat Transfer Fluids:
This chemical is utilized as a high-temperature heat transfer fluid, capitalizing on its thermal stability and heat capacity to efficiently manage temperature in industrial processes.
Used in Fragrance and Dye Production:
1,4,6-Trimethylnaphthalene is used as a component in the production of fragrances and dyes, where its chemical structure contributes to the color and scent profiles of these products.
Used in Pharmaceutical Synthesis:
It is employed in the synthesis of pharmaceuticals, indicating its importance in the development of new drugs and medicinal compounds.
Used in Insecticide Production:
1,4,6-Trimethylnaphthalene is used in the production of insecticides, highlighting its role in agricultural and pest control applications.
Used in Lubricants and Plasticizers:
This chemical is also a component in lubricants and plasticizers, where it helps to improve the flow and flexibility of these materials.
However, it is important to note that 1,4,6-trimethylnaphthalene is known for its potential toxic and carcinogenic effects. Therefore, it is crucial to handle this chemical with caution and to adhere to stringent safety guidelines to mitigate any associated risks in its applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2131-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2131-42:
(6*2)+(5*1)+(4*3)+(3*1)+(2*4)+(1*2)=42
42 % 10 = 2
So 2131-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14/c1-9-4-7-12-10(2)5-6-11(3)13(12)8-9/h4-8H,1-3H3
2131-42-2Relevant academic research and scientific papers
Synthesis of renewable alkylated naphthalenes with benzaldehyde and angelica lactone
Cong, Yu,Li, Guangyi,Li, Ning,Wang, Aiqin,Wang, Ran,Wang, Xiaodong,Xu, Jilei,Zhang, Tao
supporting information, p. 5474 - 5480 (2021/08/16)
Herein, we report a new route for the synthesis of renewable alkylated naphthalenes (ANs) with benzaldehyde and angelica lactone, two platform compounds that can be derived from lignocellulose.
Studies in catalytic dehydrogenation: Part X1 - Syntheses of alkylsubstituted spirol[4,6]undecanes and dehydrogenation of 1 -ethyl-8,9- benzospiro[4,6]undecane
Lahiri, Sikha,Pal, Panchanan,Chatterjee, Gautam,Maity, Basudev,Sen
, p. 768 - 773 (2007/10/03)
Acylation of benzene with 2-alkylsubstituted cyclopentan-l,l-diacetic anhydrides gives the keto acids (2, R = Me, Et, Prn, Pri) which are converted into the desired alkylsubstituted spiro[4,6]undecanes 5 by Paar hydrogenation followed by cyclisation and Wolff-Kishner reduction. Catalytic dehydrogenation of l-ethyl-8,9-benzospiro[4,6]undecane 5b with Pd-C gives a complex mixture of products from which a few major products like naphthalene, 2-methylnaphthalene, l-ethylnaphthalene, 1,2-dimethylnaphthalene, 1,4,6-trimethylnaphthalene, anthracene and l-methylanthracene are identified by comparative GC-mass spectra. A plausible explanation of the formation of these products is suggested.
