140615-77-6 Usage
Description
4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside (CAS# 140615-77-6) is a complex organic compound characterized by its unique chemical structure. It is a derivative of glucopyranoside, a type of sugar molecule, and features a phthalimido group and multiple benzyl and acetyl substituents. 4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is known for its potential applications in various fields due to its structural properties.
Uses
Used in Pharmaceutical Industry:
4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a building block for the synthesis of chitooligosaccharides, which have potential applications in the pharmaceutical industry. These chitooligosaccharides exhibit various biological activities, including their use as plant growth inhibitors, antimicrobials, and antineoplastics. The compound's structural diversity and functional groups make it a valuable component in the development of novel therapeutic agents.
Used in Agriculture:
In the agricultural industry, 4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a building block for the preparation of chitooligosaccharides that act as plant growth inhibitors. These inhibitors can help regulate plant growth and development, potentially leading to improved crop yields and resistance to various stress factors.
Used in Antimicrobial Applications:
4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is also used in the preparation of chitooligosaccharides with antimicrobial properties. These chitooligosaccharides can be employed in various applications, such as in the development of new antibiotics or as additives in the agricultural industry to protect plants from harmful microorganisms.
Used in Antineoplastic Applications:
Additionally, 4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used in the synthesis of chitooligosaccharides with antineoplastic properties. These compounds have the potential to be developed into novel anticancer drugs, targeting various types of cancer cells and contributing to the advancement of cancer treatment options.
Check Digit Verification of cas no
The CAS Registry Mumber 140615-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,1 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140615-77:
(8*1)+(7*4)+(6*0)+(5*6)+(4*1)+(3*5)+(2*7)+(1*7)=106
106 % 10 = 6
So 140615-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C37H35NO9/c1-24(39)45-33-31(23-43-21-25-11-5-3-6-12-25)47-37(46-28-19-17-27(42-2)18-20-28)32(34(33)44-22-26-13-7-4-8-14-26)38-35(40)29-15-9-10-16-30(29)36(38)41/h3-20,31-34,37H,21-23H2,1-2H3/t31-,32?,33?,34+,37+/m0/s1
140615-77-6Relevant articles and documents
Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals
Zinin, Alexander I.,Malysheva, Nelly N.,Shpirt, Anna M.,Torgov, Vladimir I.,Kononov, Leonid O.
, p. 627 - 630 (2008/03/13)
Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with
