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2-Propenoic acid, 3-[3-methoxy-4-[(trimethylsilyl)oxy]phenyl]-, trimethylsilyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67460-51-9

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67460-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67460-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67460-51:
(7*6)+(6*7)+(5*4)+(4*6)+(3*0)+(2*5)+(1*1)=139
139 % 10 = 9
So 67460-51-9 is a valid CAS Registry Number.

67460-51-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-trimethylsiloxy-3-methoxyphenyl)acrylic acid trimethylsilyl ester

1.2 Other means of identification

Product number -
Other names bis-trimethylsilyl trans-ferulic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67460-51-9 SDS

67460-51-9Downstream Products

67460-51-9Relevant academic research and scientific papers

Characterization of phenolic compounds in rooibos tea

Krafczyk, Nicole,Glomb, Marcus A.

, p. 3368 - 3376 (2008/09/20)

Polyphenols present in rooibos, a popular herbal tea from Aspalathus linearis, were isolated in two steps. First, phenolic ingredients were separated by multilayer countercurrent chromatography (MLCCC). Preparative high-performance liquid chromatography (HPLC) was then applied to obtain pure flavonoids. The purity and identity of isolated compounds was confirmed by different NMR experiments, HPLC-diode array detector (DAD), or gas chromatography-mass spectrometry (GC-MS) analysis. This strategy proved to be valid to isolate material in up to gram quantities and to verify known and previously not published polyphenol structures. In addition the chemistry of dihydrochalcones and related intermediates was studied. The dihydrochalcone aspalathin was oxidized to the corresponding flavanone-C-glycosides ((R)/(S)-eriodictyol-6-C-β-D-glucopyranoside and (R)/(S)-eriodictyol-8-C- β-D-glucopyranoside). Flavanone-6-C-β-D-glucopyranosides were further degraded to flavones isoorientin and orientin.

Characterization of polyphenols from plant materials through their silylation and 29Si NMR spectroscopy - Line assignment through 29Si, 13C spin-spin couplings

Schraml, Jan,Blechta, Vratislav,Sykora, Jan,Soukupova, Ludmila,Curinova, Petra,Pronek, David,Lachman, Jaromir

, p. 829 - 834 (2007/10/03)

The lines in 29Si NMR spectra of silylated polyphenols and some other compounds are difficult to assign owing to the absence of couplings with protons outside the silyl group. The assignment can be derived through small nJ(29/s

Reactivity of ferulic acid and its derivatives toward hydrogen peroxide and peracetic acid

Pan, George X.,Spencer, Liam,Leary, Gordon J.

, p. 3325 - 3331 (2007/10/03)

The reactions of ferulic acid and its derivatives with hydrogen peroxide and peracetic acid in lignin-retaining bleaching conditions have been investigated to determine their susceptibility to oxidative degradation. The conjugated side chain of ferulic acid and its etherified or esterified derivative was shown to be fairly stable, especially to hydrogen peroxide. The major reaction was trans-cis isomerization that possibly involved a radical mechanism but did not cause bond cleavage. The peracetic acid reaction increased the rate of trans-cis isomerization and was also accompanied by a minor cleavage of the side chain. Esterification did not have a substantial effect on the reactivity of ferulic acid, but 4-O- etherification significantly stabilized it against these two oxidants. By contrast, aldehyde substitution tremendously enhanced the susceptibility of the cinnamyl side chain to oxidative degradation, as evidenced by an intensive degradation of coniferaldehyde.

ASSIGNMENT OF 29Si NMR LINES AND DETERMINATION OF 29Si-13C COUPLING CONSTANTS IN PERTRIMETHYLSILYLATED LIGNIN-RELATED PHENOL-CARBOXYLIC ACIDS BY SELECTIVE HETERONUCLEAR INADEQUATE METHOD

Schraml, Jan,Past, Jaan,Puskar, Jueri,Pehk, Tonis,Lippmaa, Endel,Brezny, Robert

, p. 1985 - 1991 (2007/10/02)

Selective heteronuclear (Si-C) INADEQUATE method has been successfully used to assign all 29Si chemical shifts in six pertrimethylsilylated lignin model compounds.Empirical assignment of the lines in the region δ=23-25 to trimethylsilyl esters of carboxyl

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