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2-(trimethylsilyl)ethyl (4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-(6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

270248-07-2

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270248-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 270248-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,4 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 270248-07:
(8*2)+(7*7)+(6*0)+(5*2)+(4*4)+(3*8)+(2*0)+(1*7)=122
122 % 10 = 2
So 270248-07-2 is a valid CAS Registry Number.

270248-07-2Downstream Products

270248-07-2Relevant academic research and scientific papers

Synthetic sulfated glucuronosyl paragloboside (SGPG) and its use for the detection of autoimmune peripheral neuropathies

Chevalier, Reynald,Colsch, Beno?t,Afonso, Carlos,Baumann, Nicole,Tabet, Jean-Claude,Mallet, Jean-Maurice

, p. 563 - 577 (2006)

The sulfated glucuronosyl paragloboside SO4-3-GlcA(β1-3) Gal-(β1-4)GlcNAc(β1-3)Gal-(β1-4)Glcβ(1-1′)Cer (SGPG) is a specific constituent of the peripheral nervous system involved in human dysimmune neuropathies. Although it is highly immunogenic in human pathology, it is not a major constituent of peripheral nerve in humans. Pure SGPG is very difficult to obtain from natural sources, but is needed for the design of efficient and reproducible immunoassays. We describe a new chemical synthesis of this important glycolipid with a stearic tail, including its complete characterization by mass spectrometry and its use in the detection of autoimmune neuropathies.

Synthesis and NMR study of a heptasaccharide, epitope of the stage-specific embryonic antigen-1 (SSEA-1)

Zhang, Yongmin,Dausse, Bruno,Sinay, Pierre,Afsahi, Mohamed,Berthault, Patrick,Desvaux, Herve

, p. 231 - 241 (2007/10/03)

This paper describes an efficient synthesis of the β-2-trimethylsilylethyl glycoside of lacto-N-fucoheptaose based on a highly stereo- and regioselective glycosylation between a Lewis(x) trisaccharidic donor and a tetraol tetrasaccharidic acceptor. The ti

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