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Phosphonic acid, (3-oxo-1-phenylbutyl)-, diethyl ester, also known as DEPO, is a phosphonic acid derivative with the chemical formula C14H21O3P. It is a colorless to pale yellow liquid with a molecular weight of 266.29 g/mol. DEPO is a chiral compound, meaning it has a non-superimposable mirror image, and is used as a ligand in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. It is known for its ability to form stable complexes with metal ions, which makes it useful in catalysis and as a building block for more complex organic molecules. The compound is also recognized for its potential applications in materials science, such as in the development of new polymers and materials with unique properties. DEPO is synthesized through a series of chemical reactions and is typically handled with care due to its potential reactivity and the need for proper safety precautions.

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  • 7749-88-4 Structure
  • Basic information

    1. Product Name: Phosphonic acid, (3-oxo-1-phenylbutyl)-, diethyl ester
    2. Synonyms:
    3. CAS NO:7749-88-4
    4. Molecular Formula: C14H21O4P
    5. Molecular Weight: 284.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7749-88-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phosphonic acid, (3-oxo-1-phenylbutyl)-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonic acid, (3-oxo-1-phenylbutyl)-, diethyl ester(7749-88-4)
    11. EPA Substance Registry System: Phosphonic acid, (3-oxo-1-phenylbutyl)-, diethyl ester(7749-88-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7749-88-4(Hazardous Substances Data)

7749-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7749-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,4 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7749-88:
(6*7)+(5*7)+(4*4)+(3*9)+(2*8)+(1*8)=144
144 % 10 = 4
So 7749-88-4 is a valid CAS Registry Number.

7749-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-diethoxyphosphoryl-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names diethyl 3-oxo-1-phenylbutylphosphonate

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:7749-88-4 SDS

7749-88-4Relevant articles and documents

Preparative scale application of Mucor circinelloides ene–reductase and alcohol dehydrogenase activity for the asymmetric bioreduction of α,β-unsaturated γ-ketophosphonates

Janicki, Ignacy,Kie?basiński, Piotr,Szel?g, Jakub,G??bski, Adrian,Szcz?sna-Antczak, Miros?awa

, (2020)

The fungus Mucor circinelloides exhibits high potential for green chemistry and technological applications. Recently M. circinelloides, which so far was considered mainly as a platform for biodiesel production, was found to exhibit high ene-reductase acti

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

Dual Radical/Polar Pudovik Reaction: Application Field of New Activation Methods

Semenzin, Delphine,Etemad-Moghadam, Guita,Albouy, Dominique,Diallo, Ousmane,Koenig, Max

, p. 2414 - 2422 (2007/10/03)

The Pudovik reaction (addition of organophosphorus compounds containing a labile P-H bond with alkenes and alkynes) can progess via a radical or (and) ionic mechanism. A comparative and systematic study including various reagents and different activation methods (heating, photochemical or ultrasonic irradiation, and dry medium supported reactions) is presented. Photolysis is the most efficient method for the radical processes, but in a few examples, ultrasonic irradiation can be more appropriate since the reaction time is shorter and ultrasound did not induce side-reactions (in particular Z/E isomerization). Dry medium process on basic solid support is the best anionic activation (yield, time, selectivity, purification facilities). Ultrasound, by its mechanical effects, can contribute to increase yield compared to the classical thermal method under these basic conditions. All the activation methods are efficient whatever the unsaturated substrates for the phosphine reactivity, whereas the appropriate activation method is exclusively determined by the nature of the unsaturated system for the thiophosphine (or phosphine oxide) reactivity.

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