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144707-84-6

Benzenepropanoic acid, 4-methyl-b-(trimethylsilyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144707-84-6 Structure

  • Basic information

    1. Product Name: Benzenepropanoic acid, 4-methyl-b-(trimethylsilyl)-, ethyl ester
    2. Synonyms:
    3. CAS NO:144707-84-6
    4. Molecular Formula: C15H24O2Si
    5. Molecular Weight: 264.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144707-84-6.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: Benzenepropanoic acid, 4-methyl-b-(trimethylsilyl)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepropanoic acid, 4-methyl-b-(trimethylsilyl)-, ethyl ester(144707-84-6)
    11. EPA Substance Registry System: Benzenepropanoic acid, 4-methyl-b-(trimethylsilyl)-, ethyl ester(144707-84-6)

  • 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: 144707-84-6(Hazardous Substances Data)

144707-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144707-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144707-84:
(8*1)+(7*4)+(6*4)+(5*7)+(4*0)+(3*7)+(2*8)+(1*4)=136
136 % 10 = 6
So 144707-84-6 is a valid CAS Registry Number.

144707-84-6Downstream Products

144707-84-6Relevant articles and documents

Electroreductive silylation of activated olefins using a reactive metal anode

Ohno,Nakahiro,Sanemitsu,Hirashima,Nishiguchi

, p. 5515 - 5516 (1992)

Electroreductive silylation of α, β-unsaturated esters, nitriles and ketones in the presence of Me3SiCl using a reactive metal anode (Mg, Zn, Al) in an undivided cell afforded the corresponding β-silyl compounds offering a valuable method for introduction of a silyl group into activated olefins.

Catalyst-Free and Solvent-Controlled Reductive Coupling of Activated Vinyl Triflates with Chlorotrimethylsilane by Magnesium Metal and Its Synthetic Application

Maekawa, Hirofumi,Noda, Katsuaki,Kuramochi, Keisuke,Zhang, Tianyuan

supporting information, p. 1953 - 1956 (2018/04/16)

Vinylsilanes were directly prepared from the corresponding vinyl triflates under magnesium-promoted reductive conditions in THF with no transition metal catalyst, and gem-bis-silylated compounds were obtained in NMP. Investigation of the redox potential o

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