125185-25-3

Basic information

• Product Name: 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE
• Synonyms: 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE;DIETHYL 4-FORMYLBENZYLPHOSPHONATE;4-(Diethoxyphosphorylmethyl)benzaldehyde;4-(Diethylphosphonomethyl)benzaldehyde, tech.
• CAS NO: 125185-25-3
• Molecular Formula: C₁₂H₁₇O₄P
• Molecular Weight: 256.23
• Mol File: 125185-25-3.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE(125185-25-3)
• EPA Substance Registry System: 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE(125185-25-3)

Safety Data

• Hazardous Substances Data: 125185-25-3(Hazardous Substances Data)

Usage

General Description

4-(Diethylphosphonomethyl)benzaldehyde is a chemical compound with the molecular formula C14H19O2P. It is a benzaldehyde derivative that contains a phosphonomethyl group and two ethyl groups. 4-(DIETHYLPHOSPHONOMETHYL)BENZALDEHYDE is commonly used in the synthesis of pharmaceuticals, agrochemicals, and material sciences. It is also employed as a building block in the production of various organic compounds. Additionally, 4-(diethylphosphonomethyl)benzaldehyde has been studied for its potential applications in medical research and drug development. Its unique structure and properties make it a valuable component in the field of organic chemistry and chemical engineering.

Upstream product

• 125185-26-4 diethyl (4-(hydroxymethyl)benzyl)phosphonate 
• 104-81-4 4-Methylbenzyl bromide 
• 60-29-7 diethyl ether 
• 28149-48-6 4-[(diethoxyphosphinyl)methyl]benzoic acid 
• 6232-88-8 4-bromomethylbenzoic Acid 
• 17201-43-3 4-cyanobenzyl bromide 
• 3762-25-2 diethyl 4-methylbenzylphosphonate 
• 623-25-6 p-Xylylene dichloride 
• 25596-72-9 diethyl <4-(chloromethyl)benzyl> phosphonate 
• 108228-81-5 4-(diethoxyphosphorylmethyl)-1-bromomethyl-phenyl 
• 51359-78-5 4-(bromomethyl)benzaldehyde 
• 122-52-1 triethyl phosphite 

Downstream Products

• 683209-00-9 [4-((S)-1-Hydroxy-but-3-enyl)-benzyl]-phosphonic acid diethyl ester 
• 683209-03-2 {4-[(R)-1-(3-{1-[(S)-2-Carbamoyl-1-((S)-2-naphthalen-1-ylmethyl-pent-4-enylcarbamoyl)-ethylcarbamoyl]-cyclohexyl}-ureido)-but-3-enyl]-benzyl}-phosphonic acid diethyl ester 
• 683209-04-3 [4-((E)-(10R,15S,19S)-19-Carbamoylmethyl-15-naphthalen-1-ylmethyl-8,18,21-trioxo-7,9,17,20-tetraaza-spiro[5.15]henicos-12-en-10-yl)-benzyl]-phosphonic acid diethyl ester 
• 683209-05-4 [4-((Z)-(10R,15S,19S)-19-Carbamoylmethyl-15-naphthalen-1-ylmethyl-8,18,21-trioxo-7,9,17,20-tetraaza-spiro[5.15]henicos-12-en-10-yl)-benzyl]-phosphonic acid diethyl ester 
• 683208-97-1 [4-((R)-1-Phenoxycarbonylamino-but-3-enyl)-benzyl]-phosphonic acid diethyl ester 
• 340741-62-0 (4-diethoxymethyl-benzyl)-phosphonic acid diethyl ester 
• 651301-26-7 5-[4-(diethoxyphosphorylmethyl)phenyl]dipyrromethane 

Relevant articles and documents

Oligo(phenylene vinylene)-poly(methylstyrene) hybrids: Controlled step-wise molecular wiring of oligo(phenylene vinylene)

Well defined oligo(phenylene vinylene) grafted polymers known as oligo(phenylene vinylene)-poly(methylstyrene) hybrids have been developed using a step-wise synthetic protocol, where the length of the OPV can be controlled systematically to achieve specif

Synthesis of phosphono-substituted porphyrin compounds for attachment to metal oxide surfaces

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Enantioselective Synthesis of Metathesis-Derived Ureapeptoid Macrocycles

Ring-closing metathesis (RCM) was used for the preparation of the first member of a new class of ureapeptoid-containing macrocycles. Key to the approach was the enantioselective synthesis of functionalized carbamoyl alkenylglycine equivalents using (-)-B-allyldiisopinocampheylborane [(-)-d-Ipc2Ball]-mediated asymmetric allylation.