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N-(benzyloxycarbonyl)aminopropyl α-L-rhamnopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148404-65-3

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148404-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148404-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 148404-65:
(8*1)+(7*4)+(6*8)+(5*4)+(4*0)+(3*4)+(2*6)+(1*5)=133
133 % 10 = 3
So 148404-65-3 is a valid CAS Registry Number.

148404-65-3Relevant academic research and scientific papers

Synthesis and biological evaluation of a trisaccharide repeating unit derivative of Streptococcus pneumoniae 19A capsular polysaccharide

Morelli, Laura,Fallarini, Silvia,Lombardi, Grazia,Colombo, Cinzia,Lay, Luigi,Compostella, Federica

, p. 5682 - 5690 (2018)

Streptococcus pneumoniae (SP) is a common human pathogen associated with a broad spectrum of diseases and it is still a leading cause of mortality and morbidity worldwide, especially in children. Moreover, SP is increasingly associated with drug resistance. Vaccination against the pathogen may thus represent an important strategy to overcome its threats to human health. In this context, revealing the molecular determinants of SP immunoreactivity may be relevant for the development of novel molecules with therapeutic perspectives as vaccine components. Serogroup 19 comprises the immune-cross reactive types 19F, 19A, 19B and 19C and it accounts for a high percentage of invasive pneumococcal diseases, mainly caused by serotypes 19F and 19A. Herein, we report the synthesis and biological evaluation of an aminopropyl derivative of the trisaccharide repeating unit of SP 19A. We compare two different synthetic strategies, based on different disconnections between the three monosaccharides which make up the final trisaccharide, to define the best approach for the preparation of the trisaccharide. Synthetic accessibility to the trisaccharide repeating unit lays the basis for the development of more complex biopolymer as well as saccharide conjugates. We also evaluate the binding affinity of the trisaccharide for anti-19A and anti-19F sera and discuss the relationship between the chemical properties of the trisaccharide unit and biological activity.

Iodonium ion-assisted synthesis of a haptenic tetrasaccharide fragment corresponding to the inner cell-wall glycopeptidolipid of Mycobacterium avium serotype 4

Zuurmond, Helene M.,Veeneman, Gerrit H.,Marel, Gijs A. van der,Boom, Jacques H. van

, p. 153 - 164 (2007/10/02)

Condensation of ethyl 2,4-di-O-benzoyl-1-thio-α-L-rhamnopyranoside with ethyl 3-O-benzyl-4-O-chloroacetyl-2-O-methyl-1-thio-β-L-fucopyranoside in the presence of iodonium di-sym-collidine perchlorate afforded exclusively ethyl 2,4-di-O-benzoyl-3-O-(3-O-be

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