121869-53-2 Usage
Uses
Used in Pharmaceutical Industry:
2,4-dibromo-5-methoxyresorcinol is used as a starting material for the preparation of various pharmaceuticals, leveraging its unique structure and properties to contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dibromo-5-methoxyresorcinol serves as a key building block in the synthesis of agrochemicals, playing a crucial role in the creation of effective and environmentally friendly products for agricultural applications.
Used in Dye and Pigment Synthesis:
2,4-dibromo-5-methoxyresorcinol is utilized as a precursor in the synthesis of dyes and pigments, capitalizing on its chemical structure to produce a wide range of colorants for various industries, including textiles, plastics, and printing inks.
Used in Advanced Material Development:
2,4-dibromo-5-methoxyresorcinol also finds application in the development of advanced materials, such as polymers and composites, where its unique properties contribute to enhanced performance and functionality.
Used in Cosmetic Industry:
In the cosmetic sector, 2,4-dibromo-5-methoxyresorcinol is employed for its potential biological activity, being studied for its therapeutic properties in the treatment of various skin conditions and as an ingredient in cosmetic formulations.
Overall, 2,4-dibromo-5-methoxyresorcinol's diverse applications across different industries underscore its significance as a versatile and valuable chemical compound with broad potential for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 121869-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121869-53:
(8*1)+(7*2)+(6*1)+(5*8)+(4*6)+(3*9)+(2*5)+(1*3)=132
132 % 10 = 2
So 121869-53-2 is a valid CAS Registry Number.
121869-53-2Relevant academic research and scientific papers
Bromophloroglucinols and their methyl ethers
Kiehlmann, E.,Lauener, R. W.
, p. 335 - 344 (2007/10/02)
All 16 bromination products of phloroglucinol and its methyl ethers, as well as five bromoresorcinols and three of their dimethyl ethers, were synthesized and analyzed by nuclear magnetic resonance spectroscopy.Two or three equivalents of bromine convert phloroglucinol to di- and tribromophloroglucinol, 5-methoxyresorcinol to the tri- and 2,4-dibromo, 3,5-dimethoxyphenol to the tri- and 2,6-dibromo, and 1,3,5-trimethoxybenzene to the dibromo compound.With one equivalent of bromine, 3,5-dimethoxyphenol reacts preferentially at C-2 while 5-methoxyresorcinol gives both monobromo isomers.Partial debromination with sodium sulfite yields successively 2,4-dibromo- and 2-bromo-5-methoxyresorcinol from the tribromo compound but fails with brominated 3,5-dimethoxyphenol.In the resorcinol series, C-2 is invariably the least reactive position. 4,6-Dibromo-5-methoxyresorcinol and 2,4-dibromo-3,5-dimethoxyphenol are accessible by methylation of dibromophloroglucinol, obtained from 3,5-dibromo-2,4,6-trihydroxybenzoic acid by decarboxylation.In contrast to resorcinol and tribromoresorcinol, the partial bromination of pholoroglucinol and debromination of tribromopholoroglucinol are not selective.The 13Cnmr spectra of bromophloroglucinol methyl ethers show characteristic downfield shifts for methoxy groups orthogonal to the aromatic ring plane.
