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p-methylphenyl 2-O-benzoyl-4,6-O-benzylidene-3-O-levulinyl-1-thio-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

258333-94-7

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258333-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 258333-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,3,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 258333-94:
(8*2)+(7*5)+(6*8)+(5*3)+(4*3)+(3*3)+(2*9)+(1*4)=157
157 % 10 = 7
So 258333-94-7 is a valid CAS Registry Number.

258333-94-7Relevant academic research and scientific papers

Determining Substrate Specificities of β1,4-Endogalactanases Using Plant Arabinogalactan Oligosaccharides Synthesized by Automated Glycan Assembly

Bartetzko, Max P.,Schuhmacher, Frank,Seeberger, Peter H.,Pfrengle, Fabian

, p. 1842 - 1850 (2017/02/10)

Pectin is a structurally complex plant polysaccharide with many industrial applications in food products. The structural elucidation of pectin is aided by digestion assays with glycosyl hydrolases. We report the automated glycan assembly of oligosaccharid

Chemical synthesis of a heparan sulfate glycopeptide: Syndecan-1

Yang, Bo,Yoshida, Keisuke,Yin, Zhaojun,Dai, Hang,Kavunja, Herbert,El-Dakdouki, Mohammad H.,Sungsuwan, Suttipun,Dulaney, Steven B.,Huang, Xuefei

, p. 10185 - 10189,5 (2012/12/12)

Finishing first: The highly complex structure of the title compound (see picture) was assembled. The protective groups utilized, as well as the sequences for formation of the glycosyl linkages and protecting group removal are critical to the success of the synthesis. This first preparation of a heparan sulfate glycopeptide lays the foundation for accessing other members of this class of molecules. Copyright

Programmable one-pot oligosaccharide synthesis

Zhang, Zhiyuan,Ollmann, Ian R.,Ye, Xin-Shan,Wischnat, Ralf,Baasov, Timor,Wong, Chi-Huey

, p. 734 - 753 (2007/10/03)

In an effort to develop a broadly applicable approach to the facile one- pot synthesis of oligosaccharides, the reactivity of a number of p- methylphenyl thioglycoside (STol) donors which are either fully protected or have one hydroxyl group exposed has b

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