25692-16-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4,6-Trimethyl phenethyl chloride is used as a precursor in the synthesis of various drugs and pharmacologically active compounds. Its reactive nature allows for the formation of a wide range of chemical derivatives, making it a valuable intermediate in the development of new medications.
Used in Agrochemical and Insecticide Production:
2,4,6-TRIMETHYL PHENETHYL CHLORIDE is utilized as a key intermediate in the production of agrochemicals and insecticides. Its reactivity and structural features enable the creation of effective pest control agents, contributing to agricultural productivity and crop protection.
Used in Fragrance and Flavor Manufacturing:
2,4,6-Trimethyl phenethyl chloride is used as a raw material in the manufacturing of fragrances and flavors due to its pleasant odor. Its aromatic nature and ability to impart desirable scents make it a popular choice in the creation of various scented products, enhancing consumer appeal and experience.
Check Digit Verification of cas no
The CAS Registry Mumber 25692-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,9 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25692-16:
(7*2)+(6*5)+(5*6)+(4*9)+(3*2)+(2*1)+(1*6)=124
124 % 10 = 4
So 25692-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15Cl/c1-8-6-9(2)11(4-5-12)10(3)7-8/h6-7H,4-5H2,1-3H3
25692-16-4Relevant academic research and scientific papers
Structure of ω-Arylalkyl Radicals: A 13C CIDNP Investigation
Olah, George A.,Krishnamurthy, V. V.,Singh, Brij P.,Iyer, Pradeep S.
, p. 955 - 963 (2007/10/02)
Thermolysis of a series of ω-arylalkanoyl m-chlorobenzoyl (and acetyl) peroxides at ca. 100 deg C in cyclohexanone and in hexachloroacetone was studied by using 13C chemically induced dynamic nuclear polarization.Analysis of the observed 13C polarizations indicate that all the three radicals (β-arylethyl, γ-arylpropyl and δ-arylbutyl) have open-chain structures with no evidence for aryl participation resulting in spirocycloalkylcyclohexadienyl radicals.
