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2-(Trimethylsiloxy)propenoic acid trimethylsilyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55191-13-4

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55191-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55191-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55191-13:
(7*5)+(6*5)+(5*1)+(4*9)+(3*1)+(2*1)+(1*3)=114
114 % 10 = 4
So 55191-13-4 is a valid CAS Registry Number.

55191-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylsilyl 2-trimethylsilyloxyprop-2-enoate

1.2 Other means of identification

Product number -
Other names trimethylsilyl 2-(trimethylsiloxy)-2-propenoate

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:55191-13-4 SDS

55191-13-4Downstream Products

55191-13-4Relevant academic research and scientific papers

A CONVENIENT SYNTHESIS OF PHOSPHOENOLPYRUVATE VIA SILYLESTER INTERMEDIATE

Sekine, Mitsuaki,Futatsugi, Tetsuaki,Yamada, Kohji,Hata, Tsujiaki

, p. 371 - 372 (1980)

Phosphoenolpyruvate was synthesized in high yield by a simple procedure starting from pyruvic acid and dimethyl trimethylsilyl phosphite through trimethylsililation, bromination, and the Perkow reaction.

Bioinspired Total Synthesis of (±)-Chaetophenol C Enabled by a Pd-Catalyzed Cascade Cyclization

Li, Yun,Zhang, Qingyu,Wang, Hongyu,Cheng, Bin,Zhai, Hongbin

supporting information, p. 4387 - 4390 (2017/08/23)

A novel Pd(II)-catalyzed cascade reaction has been developed that consists of a highly regio- and stereoselective oxa [4 + 2] cycloaddition reaction of o-alkynylbenzaldehydes and an intramolecular carboxylic group quenching of the in situ generated oxonium ion. This new reaction provides a one-step construction of the tetracyclic core structure of chaetophenol C from two simple starting materials. The developed chemistry was successfully applied to the first total synthesis of chaetophenol C and dozens of its analogues.

Silyl Phosphites. Part 20. A Facile Synthesis pf Phosphoenolpyruvate and Its Analogue Utilizing in siti Generated Trimethylsilyl Bromide

Sekine, Mitsuo,Futatsugi, Tetsuaki,Yamada, Kohji,Hata, Tsujiaki

, p. 2509 - 2514 (2007/10/02)

Phosphoenolpyruvate (PEP) has been synthesized from pyruvic acid and dimethyl trimethylsilyl phosphite in high yield by a new route which involves, successively, trimethylsilylation, bromination, and a Perkow reaction.A PEP analogue of 1-(dihydroxyphosphinyl)vinyl phosphate (1) has also been prepared.

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