140658-50-0 Usage
Uses
Used in Organic Synthesis:
2,3,4,6-Tetra-O-benzyl-1-C-dichloromethyl-D-glucopyranose is used as a protecting group for selective hydroxyl group protection in the synthesis of complex carbohydrates. Its benzyl and dichloromethyl modifications provide a stable and easily removable protecting group, facilitating the efficient and precise manipulation of carbohydrate molecules.
Used in Carbohydrate Chemistry:
In the field of carbohydrate chemistry, 2,3,4,6-Tetra-O-benzyl-1-C-dichloromethyl-D-glucopyranose is employed as a versatile reagent for the synthesis of complex carbohydrate structures. Its unique structure allows for selective protection and deprotection of hydroxyl groups, enabling chemists to control the reactivity and selectivity of carbohydrate molecules during chemical synthesis.
Used in Pharmaceutical Industry:
2,3,4,6-Tetra-O-benzyl-1-C-dichloromethyl-D-glucopyranose is utilized in the development of carbohydrate-based drugs and drug delivery systems. Its ability to protect specific hydroxyl groups in carbohydrate molecules allows for the synthesis of novel carbohydrate-based therapeutic agents with improved pharmacological properties and targeted delivery capabilities.
Used in Material Science:
In material science, 2,3,4,6-Tetra-O-benzyl-1-C-dichloromethyl-D-glucopyranose is employed in the synthesis of carbohydrate-based materials, such as polymers, gels, and nanoparticles. Its unique structure and reactivity enable the development of advanced materials with tailored properties and functions, including stimuli-responsive materials, self-assembling systems, and biocompatible materials for various applications.
Used in Analytical Chemistry:
2,3,4,6-Tetra-O-benzyl-1-C-dichloromethyl-D-glucopyranose is utilized as a derivatization agent in the analysis and characterization of carbohydrates. Its ability to selectively protect and modify hydroxyl groups in carbohydrate molecules allows for the sensitive and selective detection of carbohydrates in complex biological samples, facilitating the study of carbohydrate structures, functions, and interactions in various biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 140658-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140658-50:
(8*1)+(7*4)+(6*0)+(5*6)+(4*5)+(3*8)+(2*5)+(1*0)=120
120 % 10 = 0
So 140658-50-0 is a valid CAS Registry Number.
140658-50-0Relevant articles and documents
Synthesis method of voglibose
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, (2021/08/07)
The invention provides a synthesis method of voglibose, and solves the technical problems that in an existing synthesis method of voglibose, raw materials are difficult to obtain, high in price, large in investment, low in yield and not suitable for industrial production. The synthesis method comprises the steps: synthesizing a compound V by taking glucose monohydrate and sodium acetate as raw materials through eleven reaction steps; and preparing a compound VIII from the compound V through an addition reaction, a ring-opening reaction and an aldol condensation reaction, and thus obtaining voglibose through amination reduction of the compound VIII. The synthesis method of voglibose can be widely applied to the technical field of voglibose synthesis methods.
