4825-75-6 Usage
Description
3-METHYL-1,2-BENZISOXAZOLE, with the CAS number 4825-75-6, is a chemical compound that is characterized as a colorless liquid. It is primarily recognized for its utility in the field of organic synthesis, where it serves as a valuable building block for the creation of more complex molecules and compounds.
Uses
Used in Organic Synthesis:
3-METHYL-1,2-BENZISOXAZOLE is used as a synthetic building block for the development of various organic compounds. Its unique structure and properties make it a versatile component in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-METHYL-1,2-BENZISOXAZOLE is utilized as a key intermediate in the synthesis of novel drug candidates. Its incorporation into drug molecules can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability, leading to the development of more effective therapeutic agents.
Used in Agrochemical Industry:
3-METHYL-1,2-BENZISOXAZOLE also finds application in the agrochemical industry, where it is employed in the synthesis of new pesticides and other crop protection agents. Its unique chemical properties can contribute to the development of innovative products with improved performance and selectivity, ultimately benefiting agricultural productivity and sustainability.
Used in Specialty Chemicals:
In the specialty chemicals sector, 3-METHYL-1,2-BENZISOXAZOLE is used as a starting material for the production of various high-value chemicals. These can include dyes, pigments, and other functional materials with specific applications in industries such as textiles, plastics, and coatings. Its versatility and reactivity make it an attractive choice for the development of new and improved specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 4825-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4825-75:
(6*4)+(5*8)+(4*2)+(3*5)+(2*7)+(1*5)=106
106 % 10 = 6
So 4825-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO/c1-6-7-4-2-3-5-8(7)10-9-6/h2-5H,1H3
4825-75-6Relevant articles and documents
A divergent and selective synthesis of isomeric benzoxazoles from a single N-Cl imine
Chen, Cheng-Yi,Andreani, Teresa,Li, Hongmei
, p. 6300 - 6303 (2012/01/05)
A divergent and regioselective synthesis of either 3-substituted benzisoxazoles or 2-substituted benzoxazoles from readily accessible ortho-hydroxyaryl N-H ketimines is described. The reaction proceeds in two distinct pathways through a common N-Cl imine intermediate: (a) N-O bond formation to form benzisoxazole under anhydrous conditions and (b) NaOCl mediated Beckmann-type rearrangement to form benzoxazole, respectively. The reaction path also depends on the electronic nature of the aromatic ring, with the electron-rich aromatic rings favoring the rearrangement and the electron-deficient rings favoring the N-O bond formation. A Beckmann-type rearrangement mechanism via net [1,2]-aryl migration for the formation of 2-substituted benzoxazole is proposed.
Preparation of 1,2-Benzisoxazoles from Salicylaldoximes via Trichloroacetyl Isocyanate
Stokker, Gerald
, p. 2613 - 2615 (2007/10/02)
-
