49559-67-3 Usage
Uses
Used in Pharmaceutical Industry:
5-NITRO-BENZOOXAZOLE-2-CARBOXYLIC ACID is used as an intermediate for the synthesis of various pharmaceuticals. Its capacity to engage in diverse chemical reactions makes it instrumental in creating a wide array of medicinal compounds.
Used in Agrochemical Development:
In the agrochemical sector, 5-NITRO-BENZOOXAZOLE-2-CARBOXYLIC ACID is utilized as a key intermediate. Its role is pivotal in the synthesis of compounds that contribute to crop protection and enhancement of agricultural yields.
Used in Dye Synthesis:
5-NITRO-BENZOOXAZOLE-2-CARBOXYLIC ACID is used as a building block in the creation of different types of dyes. Its chemical properties allow for the development of a spectrum of colorants used in various industries.
Used in Research and Development:
5-NITRO-BENZOOXAZOLE-2-CARBOXYLIC ACID is employed as a component in the research and development of novel materials and chemical processes. Its presence in the lab accelerates innovation in organic chemistry and chemical engineering, paving the way for new discoveries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 49559-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,5 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49559-67:
(7*4)+(6*9)+(5*5)+(4*5)+(3*9)+(2*6)+(1*7)=173
173 % 10 = 3
So 49559-67-3 is a valid CAS Registry Number.
49559-67-3Relevant academic research and scientific papers
Direct C-H carboxylation with carbon dioxide using 1,2,3-triazol-5-ylidene copper(I) complexes
Inomata, Hiroshi,Ogata, Kenichi,Fukuzawa, Shin-Ichi,Hou, Zhaomin
supporting information; experimental part, p. 3986 - 3989 (2012/09/10)
1,2,3-Triazol-5-ylidene copper(I) complexes (tzNHC-Cu) efficiently catalyzed the direct C-H carboxylation of benzoxazole and benzothiazole derivatives with CO2 to give the corresponding esters in excellent yields after treatment with alkyl iodi
