29425-06-7

Basic information

• Product Name: Propanedioyl dichloride, (phenylmethyl)-
• CAS NO: 29425-06-7
• Molecular Formula: C10H8Cl2O2
• Molecular Weight: 231.078
• Mol File: 29425-06-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Propanedioyl dichloride, (phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioyl dichloride, (phenylmethyl)-(29425-06-7)
• EPA Substance Registry System: Propanedioyl dichloride, (phenylmethyl)-(29425-06-7)

Safety Data

• Hazardous Substances Data: 29425-06-7(Hazardous Substances Data)

Upstream product

• 616-75-1 2-benzylmalonic acid 
• 49769-78-0 2-benzyl-malonic acid dimethyl ester 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 607-81-8 diethyl 2-benzylmalonate 

Downstream Products

• 68823-23-4 3-benzyl-2,4-dioxo-3,4-dihydro-2H-pyrido[2,1-b][1,3]oxazinylium betaine 
• 17853-84-8 3-benzyl-9-phenyl-1-p-tolyl-1H-chromeno[3,2-b]pyrrol-2-one 
• 37764-76-4 3-benzyl-2,4-dioxo-3,4-dihydro-2H-benzo[4,5]thiazolo[2,3-b][1,3]thiazinylium betaine 
• 62668-77-3 3-benzyl-4-hydroxy-10H-pyrano[2,3-b]quinoline-2,5-dione 
• 19795-33-6 3-benzyl-4-hydroxy-1-morpholin-4-yl-5,6,7,8-tetrahydro-1H-quinolin-2-one 
• 92029-55-5 5-benzyl-2-ethoxy-[1,3]thiazine-4,6-dione 
• 16357-86-1 5-benzyl-6-chloro-3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-2,3-dihydro-[1,3]oxazin-4-one 
• 1163-61-7 5-benzyl-2-(2-methoxy-phenyl)-[1,3]oxazine-4,6-dione 
• 5737-34-8 5-benzyl-6-chloro-3-(4-chloro-phenyl)-[1,3]oxazine-2,4-dione 
• 38324-88-8 2-benzyl-1-hydroxy-5H-pyrano[2,3-c]isoquinoline-3,6-dione 
• 1157-86-4 5-benzyl-2-phenyl-[1,3]oxazine-4,6-dione 
• 5725-49-5 5-benzyl-6-chloro-2-phenyl-[1,3]oxazin-4-one 
• 5725-64-4 5-benzyl-6-chloro-3-cyclohexyl-[1,3]oxazine-2,4-dione 
• 92426-11-4 (5-benzyl-6-chloro-4-oxo-4H-[1,3]oxazin-2-yl)-acetic acid ethyl ester 

Relevant articles and documents

Design and synthesis of malonamide derivatives as antibiotics against methicillin-resistant staphylococcus aureus

Methicillin-resistant Staphylococcus aureus (MRSA) is a serious threat to humans. Most existing antimicrobial drugs, including the β-lactam and quinoxiline classes, are not effective against MRSA. In this study, we synthesized 24 derivatives of malonamide, a new class of antibacterial agents and potentiators of classic antimicrobials. A derivative that increases bacterial killing and biofilm eradication with low cell toxicity was created.

Novel, malonyl-derived edta analogues

Reaction of malonyl dichloride and benzylmalonyl dichloride with iminodiacetate esters has provided access to several, novel EDTA analogues.

Mesoionic Six-Membered Heterocycles, V. Reactions of 6-Oxo-6H-1,3-oxazin-3-ium-4-olates with o-Quinones and Heterocumulenes

Mesoionic 6-oxo-6H-1,3-oxazine-3-ium-4-olates (1, 7) react with o-quinones (2, 4) to give compounds 3, 5, which may result from a primary cycloaddition and subsequent loss of carbon dioxide.Phenyl isocyanate and phenylisothiocyanate react with 1h and