755710-39-5 Usage
Uses
Used in Organic Synthesis:
Ethyl 1-Thio-D-glucuronide is used as a synthetic intermediate for the development of complex organic molecules and pharmaceuticals. Its unique chemical structure allows it to be a versatile building block in the synthesis of a wide range of compounds, including those with potential applications in the medical and pharmaceutical industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl 1-Thio-D-glucuronide is used as a key component in the synthesis of various drugs and drug candidates. Its ability to form a wide range of derivatives makes it a valuable asset in the development of new medications, particularly those targeting specific diseases or conditions.
Used in Research and Development:
Ethyl 1-Thio-D-glucuronide is also employed in research and development settings, where it is used to study the properties and behavior of various organic compounds. Its unique structure and reactivity make it an ideal candidate for exploring new chemical reactions and understanding the underlying mechanisms involved in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 755710-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,5,7,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 755710-39:
(8*7)+(7*5)+(6*5)+(5*7)+(4*1)+(3*0)+(2*3)+(1*9)=175
175 % 10 = 5
So 755710-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O6S/c1-2-15-8-5(11)3(9)4(10)6(14-8)7(12)13/h3-6,8-11H,2H2,1H3,(H,12,13)/t3-,4-,5-,6?,8-/m0/s1
755710-39-5Relevant academic research and scientific papers
Preparative route to glucuronyl donors bearing temporary protecting group at O-3 via 6,3-lactonisation by Bz2O or Piv2O
Kornilov, Andrei V,Sukhova, Elena V,Nifantiev, Nikolay E
, p. 309 - 313 (2007/10/03)
Heating of non-substituted β-D-glucopyranuronic acids in the presence of pivalic or benzoic anhydride in DMF gives 4-O-monoacylated or 2,4-di-O-acylated 6,3-lactones that can be easily transformed into corresponding methyl uronates bearing free OH-groups at C-2 and C-3 or C-3 only, respectively. This method was used for preparation of selectively 3-O-protected glucuronyl donors of thioglycoside and trichloracetimidate types.
