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3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 890529-41-6 Structure
  • Basic information

    1. Product Name: 3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one
    2. Synonyms: 3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one
    3. CAS NO:890529-41-6
    4. Molecular Formula:
    5. Molecular Weight: 338.522
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 890529-41-6.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: 3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one(890529-41-6)
    11. EPA Substance Registry System: 3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutan-1-one(890529-41-6)
  • 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: 890529-41-6(Hazardous Substances Data)

890529-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 890529-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,5,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 890529-41:
(8*8)+(7*9)+(6*0)+(5*5)+(4*2)+(3*9)+(2*4)+(1*1)=196
196 % 10 = 6
So 890529-41-6 is a valid CAS Registry Number.

890529-41-6Downstream Products

890529-41-6Relevant articles and documents

Development of a stereoselective and scalable process for the preparation of a methylcyclobutanol-pyridyl ether

Kuethe, Jeffrey T.,Basu, Kallol,Orr, Robert K.,Ashley, Eric,Poirier, Marc,Tan, Lushi

, p. 938 - 944 (2018)

The evolution of a scalable process for the preparation of methylcyclobutanol-pyridyl ether 1 is described. Key aspects of this development including careful control of the stereochemistry, elimination of chromatography, and application to kilogram-scale

FUSED HETEROCYCLIC OR CARBOCYCLIC COMPOUNDS CARRYING A SUBSTITUTED CYCLOALIPHATIC RADICAL AND USE THEREOF FOR TREATING VASOPRESSIN-RELATED DISEASES

-

, (2016/03/19)

The present invention relates to novel fused heterocyclic or carbocyclic compounds of formula (I) wherein the variables are as defined in the claims and the description. The invention further relates to pharmaceutical compositions comprising these compoun

PROTEIN KINASE INHIBITORS

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Page/Page column 51; 52, (2015/06/08)

The present invention relates to a novel family of protein kinase inhibitors, more specifically the present invention is directed to inhibitors of the members of the Tec or Src protein kinase families. The present invention also relates to the processes of preparation of these compounds, their intermediates, to the pharmaceutical compositions comprising them, and to their use in the treatment of proliferative, inflammatory, autoimmune, or infectious disease, disorders, or conditions in which protein kinase activity is implicated. More particularly, the present invention relates to a compound of Formula I.

2' AND 3' - SUBSTITUTED CYCLOBUTYL NUCLEOSIDE ANALOGS FOR THE TREATMENT OF VIRAL INFECTIONS AND ABNORMAL CELLULAR PROLIFERATION

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Page/Page column 75-76, (2008/06/13)

Provided are cyclobutyl nucleosides and methods for their use in treatment of infections including Retroviridae (including HIV), Hepadnaviridae (including HBV), or Flaviviridae (including BVDV and HCV) infection, or conditions related to abnormal cellular

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