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methyl O-(2',3',4',6'-tetra-O-benzyl-1'-C-vinyl-α-D-galactopyranosyl)-(1'->6)-2,3,4-tri-O-benzyl-α-D-glucoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

352020-87-2

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352020-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352020-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,0,2 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 352020-87:
(8*3)+(7*5)+(6*2)+(5*0)+(4*2)+(3*0)+(2*8)+(1*7)=102
102 % 10 = 2
So 352020-87-2 is a valid CAS Registry Number.

352020-87-2Downstream Products

352020-87-2Relevant academic research and scientific papers

Different reaction routes found in acid-catalyzed glycosylation of endo- and exo-glycals: Competition between Ferrier rearrangement and protonation

Lin, Hui-Chang,Du, Wen-Ping,Chang, Chih-Chun,Lin, Chun-Hung

, p. 5071 - 5076 (2005)

Acid-mediated glycosylations of endo- and exo-glycals have been carried out in good to excellent yields, in which a mixture of two products is often obtained resulting from Ferrier rearrangement and protonation. The former reaction exclusively takes place

Stereoselective glycosylation of exo-glycals accelerated by Ferrier-type rearrangement.

Lin, Hui-Chang,Yang, Wen-Bin,Gu, Yu-Feng,Chen, Chen-Yin,Wu, Chung-Yi,Lin, Chun-Hung

, p. 1087 - 1089 (2007/10/03)

[reaction: see text] Owing to the driving force of the Ferrier-type rearrangement, the exo-glycals are highly reactive with various alcohols to afford glycosides and glycoconjugates with exclusive alpha-configuration. The resulting vinyl group in these gl

A facile synthesis of 1′-C-alkyl-α-disaccharides from 1-C-alkyl-hexopyranoses and methyl 1-C-methyl-hexopyranosides

Li, Xiaoliu,Ohtake, Hiro,Takahashi, Hideyo,Ikegami, Shiro

, p. 4297 - 4309 (2007/10/03)

Direct O-glycosidations using the 1-C-alkyl-2,3,4,6-tetra-O-benzyl-hexopyranoses as the glycosyl donors were carried out with a catalytic amount (0.2 equiv.) of trimethylsilyl trifluoromethanesulfonate (TMSOTf). The glycosidations proceeded α-stereoselect

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