201789-32-4 Usage
Uses
Used in Organic Synthesis:
D-Glucopyranuronic acid, methyl ester, tetrabenzoate is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable building block for the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, D-Glucopyranuronic acid, methyl ester, tetrabenzoate is used as a starting material for the synthesis of novel drug candidates. Its ability to form complex structures and interact with biological targets makes it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, D-Glucopyranuronic acid, methyl ester, tetrabenzoate is used as a precursor for the synthesis of bioactive compounds with potential applications in crop protection and pest control. Its unique properties and reactivity can be harnessed to create new agrochemicals with improved efficacy and selectivity.
Used in Specialty Chemicals:
D-Glucopyranuronic acid, methyl ester, tetrabenzoate is also used in the development of specialty chemicals, such as dyes, pigments, and functional polymers. Its versatile chemical structure allows for the creation of novel materials with unique properties and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 201789-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,7,8 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201789-32:
(8*2)+(7*0)+(6*1)+(5*7)+(4*8)+(3*9)+(2*3)+(1*2)=124
124 % 10 = 4
So 201789-32-4 is a valid CAS Registry Number.
201789-32-4Relevant academic research and scientific papers
Lergenmueller, Matthias,Lichtenthaler, Frieder W.
, p. 2132 - 2137 (2007)
Practical protocols are described for a five-step conversion of d-glucuronolactone into α-d-arabino-2-ketoglucuronyl bromides, which due to their α-selective or β-specific glycosidation, and gluco- or manno-specific carbonyl reductions of the glucurono-2-ulosides formed, are expedient indirect donor substrates for the efficient introduction of α-d-GlcA or β-d-ManA residues.
