31880-33-8 Usage
Description
.beta.-D-Mannofuranose, 1,6-anhydrois a chemical compound derived from D-mannose, a type of sugar. It features a cyclic furanose ring structure, and the 1,6-anhydromodification indicates the removal of a hydroxyl group at carbon 6, forming a six-membered cyclic ether ring. .beta.-D-Mannofuranose, 1,6-anhydrohas applications in carbohydrate chemistry and holds potential for pharmaceutical uses due to its ability to interact with biological molecules and alter their activity.
Uses
Used in Carbohydrate Chemistry:
.beta.-D-Mannofuranose, 1,6-anhydrois used as a key intermediate for the synthesis of various glycoside derivatives. Its unique cyclic structure allows for the creation of a wide range of complex carbohydrates with potential applications in different industries.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, .beta.-D-Mannofuranose, 1,6-anhydrois used as a building block for the development of novel drugs. Its ability to interact with biological molecules makes it a promising candidate for the design of new therapeutic agents targeting various diseases and conditions.
Used in Research and Development:
.beta.-D-Mannofuranose, 1,6-anhydrois also utilized in research and development settings to study the structure and function of carbohydrates and their interactions with biological systems. This knowledge can lead to a better understanding of carbohydrate-related processes and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 31880-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,8,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31880-33:
(7*3)+(6*1)+(5*8)+(4*8)+(3*0)+(2*3)+(1*3)=108
108 % 10 = 8
So 31880-33-8 is a valid CAS Registry Number.
31880-33-8Relevant articles and documents
Selective synthesis of 1,6-anhydro-β-D-mannopyranose and -mannofuranose using microwave-assisted heating
Hoai, Nguyen To,Sasaki, Akiyoshi,Sasaki, Masahide,Kaga, Harumi,Kakuchi, Toyoji,Satoh, Toshifumi
experimental part, p. 1747 - 1751 (2011/12/02)
The dehydration of D-mannose and the demethanolization of methyl-α-D-mannopyranoside (MαMP) or methyl-α-D- mannofuranoside (MαMF) were examined using microwave-assisted heating for a 3-min irradiation at temperature from 120 to 280 °C in ordinary or dry sulfolane without any catalyst. The microwave-assisted heating of MαMP and MαMF smoothly proceeded to selectively afford the anhydromannoses, 1,6-anhydro-β-D-mannopyranose (AMP) and 1,6-anhydro-β-D-mannofuranose (AMF), respectively, in high yields. For MαMP in ordinary sulfolane at 240 °C, AMP was selectively obtained in the AMF:AMP ratio of 4:96, whereas AMF was the major product at the AMF:AMP ratio of 97:3 from MαMF in dry sulfolane at 220 °C.
