1221151-98-9 Usage
Description
2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl ortho-(hex-1-ynyl)benzoate is a protected D-glucopyranose derivative, which is a type of sugar molecule with a unique chemical structure. The molecule is characterized by the presence of four benzoyl groups attached to the 2, 3, 4, and 6 positions of the glucopyranose ring, as well as a hex-1-ynyl group attached to the ortho position of a benzoate group. This specific structure provides a versatile platform for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl ortho-(hex-1-ynyl)benzoate is used as a building block for the synthesis of complex carbohydrate-based pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, such as targeting specific receptors or enzymes involved in various diseases.
Used in Chemical Synthesis:
In the field of organic chemistry, 2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl ortho-(hex-1-ynyl)benzoate serves as an intermediate in the synthesis of various organic compounds. Its hex-1-ynyl group can be used for further functionalization, enabling the creation of new molecules with specific properties and applications.
Used in Material Science:
2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl ortho-(hex-1-ynyl)benzoate can be utilized in the development of novel materials with unique properties. Its ability to form stable structures and interact with other molecules makes it a promising candidate for the creation of advanced materials, such as polymers, coatings, and sensors.
Used in Analytical Chemistry:
This protected D-glucopyranose derivative can be employed as a reference compound or standard in analytical chemistry. Its distinct structure and properties make it suitable for use in various analytical techniques, such as chromatography, mass spectrometry, and nuclear magnetic resonance (NMR) spectroscopy, to study and characterize complex mixtures and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 1221151-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,1,5 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1221151-98:
(9*1)+(8*2)+(7*2)+(6*1)+(5*1)+(4*5)+(3*1)+(2*9)+(1*8)=99
99 % 10 = 9
So 1221151-98-9 is a valid CAS Registry Number.
1221151-98-9Relevant articles and documents
Glycosylation initiated cationic ring-opening polymerization of tetrahydrofuran to prepare neo-glycopolymers
Li, Yao,Yu, Biao
supporting information; experimental part, p. 6060 - 6062 (2010/11/02)
An unprecedented and highly efficient glycosylation initiated cationic ring-opening polymerization (CROP) of tetrahydrofuran is disclosed employing glycosyl ortho-hexynylbenzoates as donors and gold(i) as a catalyst, that provides an easy access to novel glycopolymers which could self-assemble into nanostructures.
