104206-20-4 Usage
Description
.beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)is a chemical compound derived from glucose, featuring a six-membered ring structure with a chlorine atom and a phenylmethyl group attached to the carbon atom. .beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)has potential applications in various fields due to its unique structure and functional groups.
Uses
Used in Carbohydrate Chemistry:
.beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)is used as a key intermediate in the synthesis of complex carbohydrates and glycoconjugates for [application reason] its ability to serve as a building block for creating more intricate carbohydrate structures.
Used in Pharmaceutical Development:
.beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)is used as a starting material or a structural component in the development of new pharmaceuticals and bioactive compounds for [application reason] its unique functional groups, which can be exploited to design novel drug candidates with specific biological activities.
Used in Chemical Biology Research:
.beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)is used as a research tool in chemical biology for [application reason] its potential to help study carbohydrate-protein interactions, which are crucial for understanding various biological processes and the development of targeted therapies.
Used in the Synthesis of Glycoconjugates:
In the field of glycobiology, .beta.-D-Glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl)is used as a precursor for the synthesis of glycoconjugates for [application reason] its structural features that facilitate the attachment of carbohydrate moieties to other biomolecules, such as proteins or lipids, to study their biological functions and potential applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 104206-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104206-20:
(8*1)+(7*0)+(6*4)+(5*2)+(4*0)+(3*6)+(2*2)+(1*0)=64
64 % 10 = 4
So 104206-20-4 is a valid CAS Registry Number.
104206-20-4Relevant articles and documents
Synthesis of 6-deoxy-6-phenylisofagomine derivatives
Lohse, Anders,Bols, Mikael
, p. 6917 - 6924 (2007/10/03)
2-Benzyl-N-tert-butoxycarbonyl-1,5-imino-1,2,5-trideoxy-D- xylitol (4) and 5-amino-4-benzyl-4,5-dideoxy-L-xylose (13) were prepared in optically pure form.
1,6-Anhydro-β-D-glucopyranose in organic synthesis: preparation of a fragment for the synthesis of rosaramycin
Procter, Garry,Genin, Denis,Challenger, Stephen
, p. 81 - 92 (2007/10/02)
1,6-Anhydro-β-D-glucopyranose has been used as the starting material for a synthesis of ethyl (E)-4-C-allyl-2,3,4,6-tetradeoxy-5,7-O-isopropylidene-8-O-methanesulphonyl-2,6-di-C-methyl-D-gulooct-2-enonate, which represents a synthetic unit equivalent to C-2/9 of the macrolide antibiotic rosaramycin.The synthesis involved a minimum of chromatography, and the extremely high level of regiochemical and stereochemical control was achieved by the use of epoxides at crucial C-C-bond-forming steps.A method was also developed, using tosylmethyl isocyanide, which converted a carbohydrate 6-aldehyde (19) directly into the corresponding homologated methyl ether.
