104206-20-4 Usage
General Description
Beta-D-glucopyranose, 1,6-anhydro-2-chloro-2-deoxy-4-O-(phenylmethyl) is a chemical compound that is derived from glucose. It consists of 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 carbohydrate chemistry, specifically in the synthesis of complex carbohydrates and glycoconjugates. The presence of the chlorine and phenylmethyl groups can also make it useful in the development of new pharmaceuticals and bioactive compounds. Additionally, it may have utility in chemical biology research and the study of carbohydrate-protein interactions.
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.
