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Diethyl 3-amino-3-oxopropylphosphonate is a chemical compound with the molecular formula C7H16NO4P. It is an organic phosphorus compound that features a phosphonate group, which is a key structural element in many biologically active molecules. diethyl 3-aMino-3-oxopropylphosphonate is characterized by its amino group, which is essential for its reactivity and potential applications in the synthesis of various pharmaceuticals and agrochemicals. The presence of the amino group also makes it a versatile building block for the creation of more complex molecules. Diethyl 3-amino-3-oxopropylphosphonate is used in the synthesis of compounds that target specific enzymes or receptors, making it a valuable intermediate in the development of new drugs and chemical agents. Its stability and reactivity are properties that are harnessed in the design of molecules with specific biological activities.

2526-67-2

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2526-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2526-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2526-67:
(6*2)+(5*5)+(4*2)+(3*6)+(2*6)+(1*7)=82
82 % 10 = 2
So 2526-67-2 is a valid CAS Registry Number.

2526-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 3-amino-3-oxopropylphosphonate

1.2 Other means of identification

Product number -
Other names Diaethyl-[2-carbamoylaethyl]phosphonat

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:2526-67-2 SDS

2526-67-2Relevant academic research and scientific papers

Comparison of catalytic activity of hexamethyltriamino- and tri-n-butylphosphines in the Pudovik reaction

Salin, Alexey V.,Il’in, Anton V.

, p. 355 - 356 (2019/01/04)

The catalytic activity of hexamethyltriaminophosphine in the P(O)–H bond addition to electron-deficient alkenes was studied. Depending on the nature of the alkene, hexamethyltriaminophosphine produces better or lower yields of the reaction products compared to tri-n-butylphosphine.

Novel lanthanide amides incorporating neutral pyrrole ligand in a constrained geometry architecture: Synthesis, characterization, reaction, and catalytic activity

Wang, Fenhua,Wang, Shaowu,Zhu, Xiancui,Zhou, Shuangliu,Miao, Hui,Gu, Xiaoxia,Wei, Yun,Yuan, Qingbing

, p. 3920 - 3931 (2013/08/23)

The first series of lanthanide amido complexes incorporating a neutral pyrrole ligand in a constrained geometry architecture were synthesized, and their bonding, reactions, and catalytic activities were studied. Treatment of [(Me3Si)2/sub

Stereodefined dinucleoside (3′,5′)-propionamidophosphonates and β-cyanoethylphosphonates and their incorporation into modified oligonucleotides

Wozniak, Lucyna A.,Bukowiecka-Matusiak, Malgorzata,Burzynska-Pedziwatr, Izabela,Stec, Wojciech J.

scheme or table, p. 2620 - 2623 (2009/08/09)

Base-catalyzed stereospecific anti-Markovnikov addition of dinucleoside (3′,5′)-H-phosphonates to the activated alkenes acrylamide and acrylonitrile resulting in the synthesis of P-chiral diastereomerically pure dinucleoside (3′,5′)-alkylphosphonates is reported.

One-pot synthesis of γ-hydroxy-γ-oxaphosphonates using pentacovalent oxaphosphorane chemistry

Hwang, Jae-Min,Islam, Tasneem,Jung, Kang-Yeoun

body text, p. 6076 - 6078 (2010/03/03)

P(V)-2,2,2-triethoxy-2,2-dihydro-5-methoxy-1,2λ5-oxaphospholene was synthesized as a new type of enolate which was hydrolyzed to give a series of phosphonates. In addition, aldol reaction of the oxaphospholene intermediate with several aldehyde

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