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Phosphonic acid, 2-propenyl-, bis(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28995-21-3

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28995-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28995-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,9 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28995-21:
(7*2)+(6*8)+(5*9)+(4*9)+(3*5)+(2*2)+(1*1)=163
163 % 10 = 3
So 28995-21-3 is a valid CAS Registry Number.

28995-21-3SDS

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 [phenylmethoxy(prop-2-enyl)phosphoryl]oxymethylbenzene

1.2 Other means of identification

Product number -
Other names Dibenzylallylphosphonat

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:28995-21-3 SDS

28995-21-3Downstream Products

28995-21-3Relevant academic research and scientific papers

Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction

Fokin, Andrey A.,Yurchenko, Alexander G.,Rodionov, Vladimir N.,Gunchenko, Pavel A.,Yurchenko, Raisa I.,Reichenberg, Armin,Wiesner, Jochen,Hintz, Martin,Jomaa, Hassan,Schreiner, Peter R.

, p. 4379 - 4382 (2007)

The antimalarial drug FR900098 was prepared from diethyl allylphosphonate involving the nitroso-ene reaction with nitrosocarbonyl methane as the key step followed by hydrogenation and dealkylation. The utilization of dibenzyl allylphosphonate as the start

Synthesis of Benzothiophene-Containing 10- and 11-Membered Cyclic Phostones

Matralis, Alexios N.,Tsantrizos, Youla S.

, p. 3728 - 3736 (2016/08/16)

Phosphinate and phosphonate derivatives can serve as useful transition-state analogues of proteases, as substrate mimics of DNA/RNA-processing enzymes, and as inhibitors of enzymes catalyzing the biosynthesis of isoprenoids. Synthetic methodologies for the preparation of medium-sized ring phosphonate-containing compounds (also known as phostones are currently limited to a few examples. A synthetic protocol was developed that is amenable to the parallel synthesis of structurally diverse phostones containing a benzo[b]thiophene core, which enables the profiling of such novel compounds in biological screens of potential therapeutic targets.

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