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4-amino-4-phosphonobutyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18865-31-1

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18865-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18865-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18865-31:
(7*1)+(6*8)+(5*8)+(4*6)+(3*5)+(2*3)+(1*1)=141
141 % 10 = 1
So 18865-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H10NO5P/c5-3(11(8,9)10)1-2-4(6)7/h3H,1-2,5H2,(H,6,7)(H2,8,9,10)

18865-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-4-phosphonobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-Amino-4-phosphonobutyric 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:18865-31-1 SDS

18865-31-1Downstream Products

18865-31-1Relevant academic research and scientific papers

METHOD FOR THE SYNTHESIS OF ALPHA-AMINOALKYLENEPHOSPHONIC ACID

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Page/Page column 23, (2014/02/15)

The present invention is related to a new method for the synthesis of alpha-aminoalkylenephosphonic acid or its phosphonate esters comprising the steps of forming a reaction mixture by mixing a P-O-P anhydride moiety comprising compound, having one P-atom at the oxidation state (+111) and the other P-atom at the oxidation state (+111) or (+V), an aminoalkanecarboxylic acid and an acid catalyst, wherein said reaction mixture comprises an equivalent ratio of alpha-aminoalkylene carboxylic acid to P-O-P anhydride moieties of at least 0.2, and recovering the resulting alpha-aminoalkylene phosphonic acid compound or an ester thereof from the reaction mixture.

A PRACTICAL SYNTHESIS OF α-AMINOPHOSPHONIC ACIDS

Genet, J. P.,Uziel, J.,Port, M.,Touzin, A. M.,Roland, S.,et al.

, p. 77 - 80 (2007/10/02)

The preparation of diterbutyl-N (diphenylmethylene) aminomethylphosphonate 3 in four steps (42percent overall yield) from N-hydroxymethyl phthalimide 1 is described.Various α substituted α-aminophosphonic acids 5 containing functionalized unsaturated chains have been synthesized by alkylation of 3 under phase transfer catalysis with halides, Michael acceptors and palladium promoted reactions, followed by mild hydrolysis. Key words: Schiff bases of diterbutylaminomethylphosphonate; phase transfer catalysis; palladium-catalyzed allylic substitution; Michael additions.

ORGANISCHE PHOSPHORVERBINDUNGEN. 79. HERSTELLUNG UND EIGENSCHAFTEN VON &α-AMINO-ω-CARBOXYALKYLPHOSPHON- UND PHOSPHINSAEUREN

Diel, Peter J.,Maier, Ludwig

, p. 201 - 210 (2007/10/02)

The synthesis, chemical and spectral properties of α-amino-ω-carboxyalkylphosphonic acids, (HO)2P(O)CH(NH2)(CH2)xCO2H, x=2 to 6, and α-amino-ω-carboxyalkyl-methylphosphonic acids CH3(HO)P(O)CH(NH2)(CH2)xCO2H, x=2 to 6 are described and the fungicidal acti

New Phosphonic Analogs of Aspartic and Glutamic Acid by Aminoalkylation of Trivalent Phosphorus Chlorides with Ethyl Acetyloacetate or Ethyl Levulinate and Benzyl Carbamate

Oleksyszyn, Jozef,Gruszecka, Ewa,Kafarski, Pawel,Mastalerz, Przemyslaw

, p. 59 - 72 (2007/10/02)

Preparation of the phosphonic analogs of α-methylaspartic (4 a-d), glutamic (7 a-b) and α-methylpyroglutamic (5 a-b) acids by aminoalkylation of trivalent phosphorus chlorides with ethyl esters of oxoalkyloacids and benzyl carbamate is described.The phosp

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