41881-07-6 Usage
Uses
1. Used in Biochemical Research:
Methyl2,3,6-tri-O-benzoyl-4-deoxy-4-chloro-a-D-glucopyranoside is used as a research tool for investigating the binding site in glycogen phosphorylase. This application is significant because it helps scientists understand the enzyme's structure, function, and mechanism of action, which can be crucial for developing targeted therapies and drugs.
2. Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its biochemical applications, Methyl2,3,6-tri-O-benzoyl-4-deoxy-4-chloro-a-D-glucopyranoside could potentially be used in the pharmaceutical industry for the development of drugs targeting glycogen phosphorylase or related enzymes. This could be particularly relevant in conditions where glycogen metabolism is dysregulated, such as certain metabolic disorders or diseases.
Chemical Properties:
Methyl2,3,6-tri-O-benzoyl-4-deoxy-4-chloro-a-D-glucopyranoside is described as a brown solid, indicating its physical state and color. This information is essential for handling, storage, and identification purposes in a laboratory or industrial setting.
Check Digit Verification of cas no
The CAS Registry Mumber 41881-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41881-07:
(7*4)+(6*1)+(5*8)+(4*8)+(3*1)+(2*0)+(1*7)=116
116 % 10 = 6
So 41881-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H25ClO8/c1-33-28-24(37-27(32)20-15-9-4-10-16-20)23(36-26(31)19-13-7-3-8-14-19)22(29)21(35-28)17-34-25(30)18-11-5-2-6-12-18/h2-16,21-24,28H,17H2,1H3/t21?,22-,23+,24+,28+/m1/s1
41881-07-6Relevant academic research and scientific papers
DESIGN AND REACTIVITY OF ORGANIC FUNCTIONAL GROUPS: IMIDAZOLYLSULFONATE (IMIDAZYLATE) - AN EFFICIENT AND VERSATILE LEAVING GROUP
Hanessian, Stephen,Vatele, Jean-Michel
, p. 3579 - 3582 (2007/10/02)
The preparation and reactivity of the novel imidazolylsulfonate group is described.