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2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 809238-84-4 Structure
  • Basic information

    1. Product Name: 2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol
    2. Synonyms: 2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol
    3. CAS NO:809238-84-4
    4. Molecular Formula:
    5. Molecular Weight: 264.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 809238-84-4.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: 2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol(809238-84-4)
    11. EPA Substance Registry System: 2-(4-((tert-butyldimethylsilyl)oxy)phenyl)prop-2-en-1-ol(809238-84-4)
  • 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: 809238-84-4(Hazardous Substances Data)

809238-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 809238-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,3 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 809238-84:
(8*8)+(7*0)+(6*9)+(5*2)+(4*3)+(3*8)+(2*8)+(1*4)=184
184 % 10 = 4
So 809238-84-4 is a valid CAS Registry Number.

809238-84-4Relevant articles and documents

Light-Triggered RNA Annealing by an RNA Chaperone

Panja, Subrata,Paul, Rakesh,Greenberg, Marc M.,Woodson, Sarah A.

, p. 7281 - 7284 (2015)

Non-coding antisense RNAs regulate bacterial genes in response to nutrition or environmental stress, and can be engineered for artificial gene control. The RNA chaperone Hfq accelerates antisense pairing between non-coding RNAs and their mRNA targets, by a mechanism still unknown. We used a photocaged guanosine derivative in an RNA oligonucleotide to temporally control Hfq catalyzed annealing. Using a fluorescent molecular beacon as a reporter, we observed RNA duplex formation within 15 s following irradiation (3 s) of photocaged RNA complexed with Hfq. The results showed that the Hfq chaperone directly stabilizes the initiation of RNA base pairs, and suggests a strategy for light-activated control of gene expression by non-coding RNAs.

Unexpected extension of usage of PPh3/CBr4, a versatile reagent: Isomerization of aromatic allylic alcohols

Gong, Wanchun,Liu, Yun,Xue, Jijun,Xie, Zhixiang,Li, Ying

, p. 1597 - 1599 (2013/02/23)

The PPh3/CBr4-catalyzed isomerization of 2-aromatic allylic alcohols into the corresponding saturated aldehydes or ketones has been achieved at room temperature in good to excellent yields under mild and metal-free conditions. This new methodology has been applied successfully to the synthesis of ibuprofen in four steps.

Hydantoin derivatives as inhibitors of tumor necrosis factor-alpha converting enzyme (TACE)

-

, (2008/06/13)

The present invention provides compounds of Formula (I): or a stereoisomer or pharmaceutically acceptable salt form thereof, wherein the variables L, Z0, R1, R4, R5, and R11 are defined are as defined herein, which are useful as inhibitors of matrix metalloproteinases (MMP), TNF-α converting enzyme (TACE), aggrecanase, or a combination thereof.

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