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

620172-07-8

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620172-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620172-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620172-07:
(8*6)+(7*2)+(6*0)+(5*1)+(4*7)+(3*2)+(2*0)+(1*7)=108
108 % 10 = 8
So 620172-07-8 is a valid CAS Registry Number.

620172-07-8Relevant articles and documents

Bifunctional antibiotics for targeting rRNA and resistance-causing enzymes

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Page/Page column 9-10, (2010/02/10)

A novel group of aminoglycosides which share some structural features of currently available aminoglycosides with regard to the backbone, while also having significant structural differences. The similarity enables these aminoglycosides to be highly poten

Synthesis of (R)-4,6-O-pyruvated trisaccharide related to the repeating unit of the antigen from Shigella dysenteriae type 9 in the form of its 2-(trimethylsilyl)ethyl glycoside

Roy, Samarpita,Sarkar, Sujit Kumar,Roy, Nirmolendu

, p. 137 - 140 (2007/10/03)

Starting from D-galactose, and D-mannose a trisaccharide namely 2-(trimethylsilyl)ethyl-2,3-di-O-benzoyl-4,6-O-[(R)-1-methoxycarbonylethylidene] -β-D-galactopyranosyl-(1→4)-2, 3, 6-tri-O-benzyl-β-D- mannopyranosyl-(1→4)-2,6-di-O-benzyl-3-O-(4-methoxybenzy

A new class of branched aminoglycosides: Pseudo-pentasaccharide derivatives of neomycin B

Fridman, Micha,Belakhov, Valery,Yaron, Sima,Baasov, Timor

, p. 3575 - 3578 (2007/10/03)

[Equation presented] The clinically important antibiotic neomycin B was modified at position C5″ by adding one extra sugar ring in the β-configuration, and the observed pseudo-pentasaccharides were tested against various bacterial strains, including patho

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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