73289-66-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Hydroxy-6-methyl-benzonitrile serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Hydroxy-6-methyl-benzonitrile is utilized as an intermediate for the production of agrochemicals. Its role in the synthesis of these compounds aids in the development of effective solutions for agricultural applications, such as pest control and crop protection.
Used in Dye Manufacturing:
2-Hydroxy-6-methyl-benzonitrile is employed in the manufacturing of dyes due to its chemical properties that contribute to the color and stability of the final product. Its use in this industry is essential for creating a wide range of dyes for various applications, including textiles and other industrial processes.
Used in Perfume Industry:
2-HYDROXY-6-METHYL-BENZONITRILE is also used in the production of perfumes, where its unique characteristics contribute to the creation of distinct and long-lasting fragrances. Its role in the perfume industry highlights its versatility and importance in the formulation of various scent profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 73289-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73289-66:
(7*7)+(6*3)+(5*2)+(4*8)+(3*9)+(2*6)+(1*6)=154
154 % 10 = 4
So 73289-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO/c1-6-3-2-4-8(10)7(6)5-9/h2-4,10H,1H3
73289-66-4Relevant academic research and scientific papers
Toop, Hamish D.,Brusnahan, Jason S.,Morris, Jonathan C.
, p. 8536 - 8538 (2017)
The first total synthesis of the potent antimalarial 7,3′-linked naphthylisoquinoline alkaloid dioncophylline E (1) has been completed. The synthesis proceeds in 12 steps (longest linear sequence) and in 15 % overall yield. Key transformations include an ortho-arylation of a naphthol with an aryllead triacetate to construct the sterically hindered biaryl bond, and a three-step sequence to stereoselectively generate the trans-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline moiety.
