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CAS

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1374792-92-3

2-methoxy-4-(trimethylsilyl)phenylboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374792-92-3 Structure

  • Basic information

    1. Product Name: 2-methoxy-4-(trimethylsilyl)phenylboronic acid
    2. Synonyms: 2-methoxy-4-(trimethylsilyl)phenylboronic acid
    3. CAS NO:1374792-92-3
    4. Molecular Formula:
    5. Molecular Weight: 224.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374792-92-3.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-methoxy-4-(trimethylsilyl)phenylboronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methoxy-4-(trimethylsilyl)phenylboronic acid(1374792-92-3)
    11. EPA Substance Registry System: 2-methoxy-4-(trimethylsilyl)phenylboronic acid(1374792-92-3)

  • 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: 1374792-92-3(Hazardous Substances Data)

1374792-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374792-92-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,7,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1374792-92:
(9*1)+(8*3)+(7*7)+(6*4)+(5*7)+(4*9)+(3*2)+(2*9)+(1*2)=203
203 % 10 = 3
So 1374792-92-3 is a valid CAS Registry Number.

1374792-92-3Upstream product

1374792-92-3Downstream Products

1374792-92-3Relevant articles and documents

Synthesis and extension/contraction motion of spiroborate-based double-stranded helicates consisting of substituted oligophenol strands

Miwa, Kazuhiro,Shimizu, Kaori,Min, Heejun,Furusho, Yoshio,Yashima, Eiji

supporting information; experimental part, p. 4470 - 4478 (2012/07/27)

A new class of ortho- and meta-substituted tetraphenols at the terminal phenyl residues with a biphenylene unit in the middle were synthesized and the effect of the substitution position on the spiroborate-based double-stranded helicate formation with sodium borohydride was investigated. The ortho-substitution considerably hampered the spiroborate formation between the terminal biphenol units and the boron atoms, whereas the meta-substituted oligomers formed a double-stranded helicate bridged by spiroborate groups accommodating a sodium cation in the center, which displayed an extension and contraction motion triggered by the removal and addition of sodium ions in solution.

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