65310-00-1 Usage
Description
METHYL-L-FUCOPYRANOSIDE is a compound that is useful in organic synthesis, with the chemical formula C7H12O5 and a mixture of α and β forms. It is a derivative of L-fucose, a monosaccharide found in various biological systems, and is commonly used as a building block in the synthesis of complex carbohydrates and glycoconjugates.
Uses
Used in Organic Synthesis:
METHYL-L-FUCOPYRANOSIDE is used as a building block in organic synthesis for the preparation of complex carbohydrates and glycoconjugates. Its unique structure allows for the formation of various glycosidic linkages, making it a valuable component in the synthesis of biologically active compounds and pharmaceuticals.
Used in Pharmaceutical Industry:
METHYL-L-FUCOPYRANOSIDE is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly those targeting carbohydrate-based drug discovery. Its ability to form stable glycosidic bonds with other molecules makes it an essential component in the development of new drugs with improved efficacy and selectivity.
Used in Research and Development:
METHYL-L-FUCOPYRANOSIDE is used as a research tool in the study of carbohydrate chemistry, glycobiology, and related fields. Its availability as a pure compound allows researchers to investigate the structure, function, and interactions of carbohydrates in biological systems, leading to a better understanding of their role in various diseases and biological processes.
Used in Cosmetic Industry:
METHYL-L-FUCOPYRANOSIDE can be used in the cosmetic industry as an ingredient in skincare and beauty products. Its ability to form stable glycosidic bonds with other molecules can contribute to the development of innovative formulations with enhanced properties, such as improved skin hydration, texture, and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 65310-00-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,1 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65310-00:
(7*6)+(6*5)+(5*3)+(4*1)+(3*0)+(2*0)+(1*0)=91
91 % 10 = 1
So 65310-00-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O5/c1-3-4(8)5(9)6(10)7(11-2)12-3/h3-10H,1-2H3/t3-,4+,5-,6-,7?/m0/s1
65310-00-1Relevant articles and documents
PROCESS FOR PRODUCING 2'-O-FUCOSYLLACTOSE
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Paragraph 0585, (2021/05/07)
The present invention relates to a method for preparing 2′-O-fucosyllactose, the intermediates obtainable by this method and the use of these intermediates. The preparation comprises the reaction of a protected fucose of the general formula (I) with a tri
Synthesis of Deoxyglycosides by Desulfurization under UV Light
Ge, Jian-Tao,Li, Ying-Ying,Tian, Jun,Liao, Rong-Zhen,Dong, Hai
, p. 7008 - 7014 (2017/07/15)
This study was performed to develop a highly efficient method whereby desulfurization could be completed in 0.5 h under ultraviolet light, at room temperature, and in the presence of trialkylphosphine. Using this method, deoxyglycosides could be produced from sulfur-containing glycosides in almost quantitative yields. The much higher reactivity of desulfurization with triethylphosphine versus that with triethylphosphite is also discussed.
Direct glycosylation of unprotected and unactivated sugars using bismuth nitrate pentahydrate
Polanki, Innaiah K.,Kurma, Siva H.,Bhattacharya, Asish K.
, p. 196 - 205 (2015/06/08)
Bi(NO3)3, a low-cost, mild, and environmentally green catalyst, has been successfully utilized for Fischer glycosylation for the synthesis of alkyl/aryl glycopyranosides by reacting unprotected sugars, namely, D-glucose, L-rhamnose, D-galactose, D-arabinose, and N-acetyl-D-glucosamine with various alcohols in good to excellent yields. The glycosides were formed with high α-selectivity. Further, an expedient separation of α- and β-glycosides using silver nitrate-impregnated silica gel flash liquid chromatography has been developed.
