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CAS

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288585-01-3

phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 288585-01-3 Structure

  • Basic information

    1. Product Name: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside
    2. Synonyms: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside
    3. CAS NO:288585-01-3
    4. Molecular Formula:
    5. Molecular Weight: 687.81
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 288585-01-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(288585-01-3)
    11. EPA Substance Registry System: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(288585-01-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 288585-01-3(Hazardous Substances Data)

288585-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288585-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 288585-01:
(8*2)+(7*8)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*1)=193
193 % 10 = 3
So 288585-01-3 is a valid CAS Registry Number.

288585-01-3Relevant articles and documents

Stereoselective synthesis of α- and β-C-glucosides via radical cyclization with an allylsilyl tether. Control of the stereoselectivity by changing the conformation of the pyranose ring

Shuto, Satoshi,Terauchi, Masaru,Yahiro, Yumi,Abe, Hiroshi,Ichikawa, Satoshi,Matsuda, Akira

, p. 4151 - 4155 (2000)

An efficient method for preparing both 1α- and 1β-C-glucosides having a 3-hydroxypropyl group at the anomeric position via a radical cyclization reaction with an allylsilyl tether was developed. The stereoselectivity of the radical cyclization can be cont

Synthesis of 4,8-anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate as a novel IP3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy

Terauchi, Masaru,Yahiro, Yumi,Abe, Hiroshi,Ichikawa, Satoshi,Tovey, Stephen C.,Dedos, Skarlatos G.,Taylor, Colin W.,Potter, Barry V.L.,Matsuda, Akira,Shuto, Satoshi

, p. 3697 - 3707 (2007/10/03)

4,8-Anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate (9), designed as a novel IP3 receptor ligand having an α-C-glycosidic structure, was synthesized via a radical cyclization reaction with a temporary connecting allylsilyl group as the ke

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