136759-85-8 Usage
Description
.beta.-L-Allopyranose, 1,6-anhydro-2,3-O-(phenylmethylene)-, acetate is a chemical compound derived from L-Allopyranose, a six-carbon sugar molecule. .beta.-L-Allopyranose, 1,6-anhydro-2,3-O-(phenylmethylene)-, acetate has been modified with the addition of an acetyl group and a phenylmethylene moiety, which alters its chemical properties. These modifications make it a valuable tool in pharmaceutical research and development, particularly in the field of carbohydrate-based pharmaceuticals.
Uses
Used in Pharmaceutical Research and Development:
.beta.-L-Allopyranose, 1,6-anhydro-2,3-O-(phenylmethylene)-, acetate is used as a research compound for the development of new drugs. Its unique chemical properties and potential biological activities make it a promising candidate for the creation of novel pharmaceuticals, particularly in the field of carbohydrate-based therapeutics.
Used in Drug Synthesis:
In the pharmaceutical industry, .beta.-L-Allopyranose, 1,6-anhydro-2,3-O-(phenylmethylene)-, acetate is used as a key intermediate in the synthesis of various drugs. Its specific chemical properties allow for the development of new drug candidates with improved efficacy and reduced side effects.
Used in Medicinal Chemistry:
As a valuable tool for researchers in the medicinal chemistry field, .beta.-L-Allopyranose, 1,6-anhydro-2,3-O-(phenylmethylene)-, acetate is used for studying the structure-activity relationships of carbohydrate-based compounds. This helps in the design and optimization of new drugs with better pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 136759-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136759-85:
(8*1)+(7*3)+(6*6)+(5*7)+(4*5)+(3*9)+(2*8)+(1*5)=168
168 % 10 = 8
So 136759-85-8 is a valid CAS Registry Number.
136759-85-8Relevant articles and documents
Facile Preparation of 1,6-Anhydro-2-azido-3-O-benzyl-2-deoxy-β-D-glucopyranose and Its 4-O-Substituted Derivatives
Sakairi, Nobuo,Takahashi, Shunya,Wang, Feng,Ueno, Yoshihito,Kuzuhara, Hiroyoshi
, p. 1756 - 1758 (2007/10/02)
Treatment of 1,6-anhydro-2,3-O-endo-benzylidene-β-D-mannopyranose derivatives with trimethylamine-borane (1/1)-aluminium chloride resulted in highly regioselective fission of the cyclic acetals to give the corresponding 2-O-unprotected-3-O-benzyl derivatives. Trifluoromethane-sulfonylation of these, followed by nucleophilic substitution, afforded 2-azido-2-deoxy derivatives in good yields.
