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116561-10-5

5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116561-10-5 Structure

  • Basic information

    1. Product Name: 5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one
    2. Synonyms: 5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one
    3. CAS NO:116561-10-5
    4. Molecular Formula:
    5. Molecular Weight: 228.363
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116561-10-5.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: 5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one(116561-10-5)
    11. EPA Substance Registry System: 5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5H-furan-2-one(116561-10-5)

  • 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: 116561-10-5(Hazardous Substances Data)

116561-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116561-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,6 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116561-10:
(8*1)+(7*1)+(6*6)+(5*5)+(4*6)+(3*1)+(2*1)+(1*0)=105
105 % 10 = 5
So 116561-10-5 is a valid CAS Registry Number.

116561-10-5Relevant articles and documents

Synthesis of the Dideoxynucleosides ddC and CNT from Glutamic Acid, Ribonolactone, and Pyrimidine Bases

Okabe, Masami,Sun, Ruen-Chu,Tam, Steve Y.-K.,Todaro, Louis J.,Coffen, David L.

, p. 4780 - 4786 (2007/10/02)

2,3-Dideoxyribose in suitably protected form was prepared from glutamic acid and coupled with silylated cytosine to give a mixture of the α-and β-anomers of 2',3'-dideoxycitidine.The anomer ratio depended on the Lewis acid used in the coupling, with EtAlCl2 favoring the β-anomer ddC, a potent anti-HIV drug.Conjugate addition of cyanide to a 4-butenolide prepared from D-ribonolactone gave a mixture of (racemic) α- and β-3-cyanobutyrolactones.Both isomers were reduced to lactols and coupled with thymine to give α/β-anomer pairs.The α-cyano lactone, the struct ure of which was established by X-ray crystallography, afforded an authentic sample of the putative (but in fact inactive) anti-HIV substance known in AIDS research as CNT.

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