Welcome to LookChem.com Sign In|Join Free
  • or
p-methylphenyl 2-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220645-55-6

Post Buying Request

220645-55-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

220645-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220645-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220645-55:
(8*2)+(7*2)+(6*0)+(5*6)+(4*4)+(3*5)+(2*5)+(1*5)=106
106 % 10 = 6
So 220645-55-6 is a valid CAS Registry Number.

220645-55-6Downstream Products

220645-55-6Relevant 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

One-pot strategies for the synthesis of the tetrasaccharide linkage region of proteoglycans

Huang, Teng-Yi,Zulueta, Medel Manuel L.,Hung, Shang-Cheng

supporting information; experimental part, p. 1506 - 1509 (2011/04/27)

A linker-attached tetrasaccharide corresponding to the linkage region of proteoglycans was synthesized via one-pot procedures from the silylated monosaccharide derivatives. Regioselective one-pot protection protocols were applied in generating the requisite monosaccharide building blocks whereas stereoselective one-pot glycosylation approaches were utilized to assemble the tetrasaccharide skeleton.

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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 220645-55-6