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tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152338-04-0 Structure
  • Basic information

    1. Product Name: tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether
    2. Synonyms: tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether
    3. CAS NO:152338-04-0
    4. Molecular Formula:
    5. Molecular Weight: 336.549
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152338-04-0.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: tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether(152338-04-0)
    11. EPA Substance Registry System: tert-butyldiphenylsilyl (cyclopent-3-enyl)methyl ether(152338-04-0)
  • 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: 152338-04-0(Hazardous Substances Data)

152338-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152338-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,3 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152338-04:
(8*1)+(7*5)+(6*2)+(5*3)+(4*3)+(3*8)+(2*0)+(1*4)=110
110 % 10 = 0
So 152338-04-0 is a valid CAS Registry Number.

152338-04-0Relevant articles and documents

New efficient method for the synthesis of the antiviral agent carbovir

Jung, Michael E.,Rhee, Hakjune

, p. 4449 - 4452 (1993)

An efficient synthesis of (±)-carbovir 1 and simple des(hydroxymethyl) analogues, e.g., 5, is reported which uses a new approach for attaching nucleoside bases to cycloalkene systems.

Synthesis of 4-substituted-1,2,3-triazole carbanucleoside analogues of ribavirin via click chemistry

Perez-Castro, Isabel,Caamano, Olga,Fernandez, Franco,Garcia, Marcos D.,Lopez, Carmen,De Clercq, Erik

, p. 3805 - 3813 (2008/10/09)

The synthesis and biological evaluation as antiviral agents of a series of racemic 4-aryl-1,2,3-triazolo-2′,3′-dideoxy-2′- iodocarbanucleosides and 4-aryl-1,2,3-triazolo-2′,3′-dideoxy- 2′,3′-didehydrocarbanucleosides is presented. These compounds were produced using a click chemistry approach, with the iodoazide 13a as the key intermediary. The Royal Society of Chemistry 2007.

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