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26151-16-6

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26151-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26151-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,5 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26151-16:
(7*2)+(6*6)+(5*1)+(4*5)+(3*1)+(2*1)+(1*6)=86
86 % 10 = 6
So 26151-16-6 is a valid CAS Registry Number.

26151-16-6Relevant articles and documents

Cu(ClO4)2·6H2O catalyzed solvent free per-O-acetylation and sequential one-pot conversions of sugars to thioglycosides

Chatterjee, Debnath,Paul, Abhijit,Rajkamal,Yadav, Somnath

, p. 29669 - 29674 (2015)

The solvent free per-O-acetylation of various reducing and non-reducing sugars has been carried out using stoichiometric amounts of acetic anhydride and copper(ii) perchlorate hexahydrate as the catalyst. The reactions with various reducing monosaccharides have also been followed by a one-pot sequential conversion to the corresponding thioglycosides in high yields. This journal is

2,3-Carbamate mannosamine glycosyl donors in glycosylation reactions of diacetone-D-glucose. An experimental and theoretical study

Morelli, Laura,Legnani, Laura,Ronchi, Silvia,Confalonieri, Laura,Imperio, Daniela,Toma, Lucio,Compostella, Federica

, (2021/08/26)

The role of the cyclic 2,3-N,O-carbamate protecting group in directing the selectivity of mannosylation reactions of diacetone-D-glucose, promoted by BSP/Tf2O via α-triflate intermediates, has been investigated through a combined computational

A silyl ether-protected building block forO-GlcNAcylated peptide synthesis to enable one-pot acidic deprotection

Yan, Bingjia,Li, Wenyi,Hackenberger, Christian P. R.

supporting information, p. 8014 - 8017 (2021/10/04)

In this report, we introduce a novel building block for Fmoc/tBu solid phase peptide synthesis (SPPS) of β-linkedO-GlcNAcylated peptides. This building block carries acid labile silyl ether protecting groups, which are fully removed under TFA-mediated peptide cleavage conditions from the resin, thus requiring fewer synthetic steps and no intermediate purification as compared to other acid or base labile protecting group strategies.

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