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911682-17-2

3-Buten-2-ol, 4-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-methoxyphenyl]-, (3E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 911682-17-2 Structure

  • Basic information

    1. Product Name: 3-Buten-2-ol, 4-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-methoxyphenyl]-, (3E)-
    2. Synonyms:
    3. CAS NO:911682-17-2
    4. Molecular Formula: C17H28O3Si
    5. Molecular Weight: 308.493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 911682-17-2.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-Buten-2-ol, 4-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-methoxyphenyl]-, (3E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Buten-2-ol, 4-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-methoxyphenyl]-, (3E)-(911682-17-2)
    11. EPA Substance Registry System: 3-Buten-2-ol, 4-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-methoxyphenyl]-, (3E)-(911682-17-2)

  • 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: 911682-17-2(Hazardous Substances Data)

911682-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911682-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,6,8 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 911682-17:
(8*9)+(7*1)+(6*1)+(5*6)+(4*8)+(3*2)+(2*1)+(1*7)=162
162 % 10 = 2
So 911682-17-2 is a valid CAS Registry Number.

911682-17-2Relevant articles and documents

Suppression of inducible nitric oxide synthase expression by yakuchinones and their analogues

Lee, Hwa Jin,Kim, Ji Sun,Yoon, Joung Wha,Kim, Hee-Doo,Ryu, Jae-Ha

, p. 377 - 379 (2007/10/03)

Analogues of yakuchinones were synthesized as inhibitors of nitric oxide production in lipopolysaccharideactivated macrophage cell line, RAW 264.7 cells. We prepared stronger inhibitors than the original natural molecules, yakuchinones A and B reported from Alpinia oxyphylla. From the limited structural activity relation study of analogues, we concluded that the optimal length of linker between two aryl groups and the presence of enone moiety in the linker were identified as essential for the activity. The IC50 value of the most potent structure was 0.92 μM. The active analogues suppressed the expression of inducible nitric oxide synthase protein and mRNA.

Chain-branched acyclic phenethylthiocarbamates as vanilloid receptor antagonists

Yoon, JungWha,Choi, HyeYoung,Lee, Hyun Joo,Ryu, Chong Hyun,Park, Hyeung-Geun,Suh, Young-Ger,Oh, Uhtaek,Jeong, Yeon Su,Choi, Jin Kyu,Park, Young-Ho,Kim, Hee-Doo

, p. 1549 - 1552 (2007/10/03)

A series of acyclic phenethylthiocarbamate derivatives have been synthesized, and their antagonist effect against vanilloid receptor tested. Chain branching led to a significant change in antagonist activity of the parent molecule. Ethyl-branched 1e showe

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