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allyl O-(2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-(1→6)-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

346441-53-0

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346441-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346441-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,4,4 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 346441-53:
(8*3)+(7*4)+(6*6)+(5*4)+(4*4)+(3*1)+(2*5)+(1*3)=140
140 % 10 = 0
So 346441-53-0 is a valid CAS Registry Number.

346441-53-0Relevant academic research and scientific papers

Synthetic Lipomannan Glycan Microarray Reveals the Importance of α(1,2) Mannose Branching in DC-SIGN Binding

Sawettanai, Nithinan,Leelayuwapan, Harin,Karoonuthaisiri, Nitsara,Ruchirawat, Somsak,Boonyarattanakalin, Siwarutt

, p. 7606 - 7617 (2019)

Lipomannan (LM), a glycophospholipid found on the cell surface of mycobacteria, involves the virulence and survival in host cells. However, there is little to no information on how exactly mannan alignment, including the number of mannose units and the br

Synthesis of a core arabinomannan oligosaccharide of Mycobacterium tuberculosis

Hoelemann, Alexandra,Stocker, Bridget L.,Seeberger, Peter H.

, p. 8071 - 8088 (2007/10/03)

The synthesis of a core arabinomannan (AM) oligosaccharide from Mycobacterium tuberculosis has been achieved using a convergent [6 + 6] glycosylation strategy and a defined set of building blocks. Dodecasaccharide 1, containing the key AM structural featu

Facile synthesis of a comb-like mannohexaose: A trimer of the disaccharide repeating unit of the cell-wall mannans of Aphanoascus mephitatus and related species

Heng, Linsen,Ning, Jun,Kong, Fanzuo

, p. 431 - 437 (2007/10/03)

An efficient method for the preparation of a comb-like mannohexaose having α-(1→6) and α-(1→2) linkages has been described using 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl trichloroacetimidate as the key glycosyl donor in an 'inverse Schmidt' procedure.

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