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172334-45-1

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172334-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172334-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,3,3 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 172334-45:
(8*1)+(7*7)+(6*2)+(5*3)+(4*3)+(3*4)+(2*4)+(1*5)=121
121 % 10 = 1
So 172334-45-1 is a valid CAS Registry Number.

172334-45-1Relevant articles and documents

Lipo-oligosaccharide of the Campylobacter lari type strain ATCC 35221. Structure of the liberated oligosaccharide and an associated extracellular polysaccharide

Aspinall, Gerald O.,Monteiro, Mario A.,Pang, Henrianna

, p. 245 - 264 (1995)

Lipo-oligosaccharide (LOS) from phenol-water extraction of cells of the Campylobacter lari type strain (ATCC 35221) was separated as a water-insoluble gel of low relative molecular mass (Mr) from a water-soluble extracellular polysaccharide of high Mr.Structural investigations were performed on the liberated oligosaccharide and the extracellular polysaccharide, variously using 1H, 13C, 31 P NMR spectroscopy, linkage analysis, and fast atom bombardment-mass spectrometry of permethylated derivatives of the glycans and their products of chemical and enzymic degradation.The following structures are proposed for the highly branched region of the LOS: and for the tetraglycosyl phosphate repeating unit of the extracellular polysaccharide: - -> 3)-β-D-Glc pNAc-(1 -> 2)-6-d-α-L-gul-Hep p-(1 -> 2)-3-d-β-D-threo-Pen p-(1 -> 3)-6-d-α-L-gul-Hep p->n - Keywords: Campylobacter lari type strain (ATCC 35221); Lipo-oligosaccharide; Extracellular polysaccharide; Tetraglycosyl phosphate polymer

Enantiospecific synthesis of both enantiomers of 2-benzyloxydihydropyran-3- ones from arabinose

Uhrig, Maria Laura,Varela, Oscar

, p. 893 - 898 (2007/10/03)

Approaches to the enantioselective synthesis of the useful building blocks (2R)- and (2S)-2-benzyloxy-2(H)-pyran-3(6H)-one (12 and 17, respectively) are described. The most direct and highly yielding route for the synthesis of 12 was based on the 'one-pot

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