5043-21-0 Usage
Uses
Used in Chemical Synthesis:
8-BroMo-2-naphthoic acid is used as a reagent for the preparation of substituted naphthoic acids. Its unique structure allows it to be a valuable intermediate in the synthesis of various organic compounds, particularly those with potential applications in pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 8-BroMo-2-naphthoic acid is used as a building block for the development of new drugs. Its ability to form substituted naphthoic acids can lead to the creation of novel compounds with potential therapeutic properties, making it a valuable asset in drug discovery and development.
Used in Dye Industry:
8-BroMo-2-naphthoic acid is also used in the dye industry as a precursor for the synthesis of various dyes and pigments. Its chemical structure allows for the creation of a wide range of colors, making it a versatile component in the production of dyes for textiles, plastics, and other applications.
Used in Research and Development:
In research and development settings, 8-BroMo-2-naphthoic acid serves as a key compound for studying the properties and reactions of naphthalene derivatives. Its unique structure and reactivity make it an interesting subject for scientific investigations, potentially leading to new discoveries and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 5043-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5043-21:
(6*5)+(5*0)+(4*4)+(3*3)+(2*2)+(1*1)=60
60 % 10 = 0
So 5043-21-0 is a valid CAS Registry Number.
5043-21-0Relevant academic research and scientific papers
Retinoid-like compounds
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, (2008/06/13)
This invention relates to a retinoid mpound of formula I STR1 in which Y is --CO--NH--, --CR 2 CR 3 --, --CO--O--, --O--CO--, --C( S)--NH--, --C C--, --O--CH 2 --, --CH 2 --O--, or --CH 2 --CH 2 --;A is --(CH 2) t -- or a bond;Q is phenyl optionally substituted with one to three same or different C 1-6 alkyl, C 1-6 alkoxy, halogen, or --CO 2 R 4 ;R 1 is --CO 2 Z, --CONHR 5, C 1-6 alkyl, --CH 2 OH, or --CHO;R 2, R 3, R 4, R 5, and Z are independently hydrogen or C 1-6 alkyl;t is one to six.
Novel naphthalenylalkyl-3H-1,2,3,5-oxathiadiazole 2-oxides useful as antihyperglycemic agents
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, (2008/06/13)
This invention relates to novel [(substituted naphthalenyl)alkyl]-3H-1,2,3,5-oxathiadiazole 2-oxides, to the processes for their preparation, to methods for using the compounds, and to pharmaceutical compositions thereof. The compounds have pharmaceutical
Processes for the preparation of novel naphthalenylmethyl-3H-1,2,3,5-oxathiadiazole 2-oxides useful as antihyperglycemic agents
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, (2008/06/13)
This invention relates to the processes for the production of novel [(substituted naphthalenyl)methyl]-3H-1,2,3,5-oxathiadiazole 2-oxides. The compounds have pharmaceutical properties which render them beneficial for the treatment of diabetes mellitus and
