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allyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->6)-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.

346441-54-1

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346441-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346441-54-1 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 346441-54:
(8*3)+(7*4)+(6*6)+(5*4)+(4*4)+(3*1)+(2*5)+(1*4)=141
141 % 10 = 1
So 346441-54-1 is a valid CAS Registry Number.

346441-54-1Downstream Products

346441-54-1Relevant academic research and scientific papers

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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