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Phosphonic acid, (1-amino-1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79014-69-0

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79014-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79014-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79014-69:
(7*7)+(6*9)+(5*0)+(4*1)+(3*4)+(2*6)+(1*9)=140
140 % 10 = 0
So 79014-69-0 is a valid CAS Registry Number.

79014-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-amino-1-phenylethyl)phosphonic acid

1.2 Other means of identification

Product number -
Other names (1-amino-1-phenyl-ethyl)-phosphonic 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:79014-69-0 SDS

79014-69-0Downstream Products

79014-69-0Relevant academic research and scientific papers

Synthesis of phosphinic and phosphonic analogs of aromatic amino acids

Belyankin,Khomutov,Zhukov,Kartasheva,Khomutov

, p. 133 - 136 (2007/10/03)

The reaction of aryl and aralkyl aldoximes with hypophosphorous acid resulted in aminophosphinic acids, which were oxidized into the corresponding aminophosphonic acids.

Synthesis of α-substituted α-aminophosphinic and α-aminophosphonic acids

Osipova,Belyankin,Khomutov,Zhukov,Khurs,Khomutov

, p. 2588 - 2591 (2007/10/03)

The reaction of ketoximes with hypophosphorous acid resulted in previously unknown α-substituted-α-aminophosphimc acids, which were oxidized into the corresponding α-substituted-α-aminophosphonic acids.

The Synthesis of 1-Aminoalkylphosphonic Acids. A Revised Mechanism of the Reaction of Phosphorus Trichloride, Amides and Aldehydes or Ketones in Acetic Acid (Oleksyszyn Reaction)

Soroka, Miroslaw

, p. 331 - 334 (2007/10/02)

The mechanism of the amidoalkylation of trivalent phosphorus compounds in acetic acid has been reinvestigated.Evidence is presented that 1-(acylamino)alkyl acetates 5 and not N,N'-alkylidenebisamides 2 are the intermediates in this reaction.Supporting literature analogies are discussed.This paper also describes a convenient procedure for the preparation of crude (acylamino)alkyl alkanoates 5, which are excellent amidoalkylating agents.The usefulness of these reagents is demonstrated by a simple two-step "one pot" synthesis of 1-aminoalkylphosphinic acids 1.

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