838-42-6

Basic information

• Product Name: 1,3-Dioxane, 5,5-dimethyl-2-(4-nitrophenyl)-
• Synonyms: 2-(4-nitrophenyl)-5,5-dimethyl-1,3-dioxane;5,5-dimethyl-2-(4-nitrophenyl)-[1,3]dioxane
• CAS NO: 838-42-6
• Molecular Formula: C12H15NO4
• Molecular Weight: 237.255
• Mol File: 838-42-6.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxane, 5,5-dimethyl-2-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane, 5,5-dimethyl-2-(4-nitrophenyl)-(838-42-6)
• EPA Substance Registry System: 1,3-Dioxane, 5,5-dimethyl-2-(4-nitrophenyl)-(838-42-6)

Safety Data

• Hazardous Substances Data: 838-42-6(Hazardous Substances Data)

Usage

Common uses

Organic synthesis, pharmaceutical manufacturing It is often utilized as a reagent in the synthesis of organic compounds and in the production of pharmaceuticals.

Physical properties

Colorless liquid, sweet and pleasant odor The compound appears as a colorless liquid with a sweet and pleasant smell.

Flammability

Highly flammable The compound can easily catch fire and burn, posing a potential fire hazard.

Health hazards

Harmful if swallowed, inhaled, or absorbed through the skin Ingesting, inhaling, or coming into contact with the skin can cause adverse health effects.

Irritation

Can cause eye and skin irritation The compound may lead to discomfort or damage to the eyes and skin upon contact.

Environmental concerns

Potential bioaccumulation in aquatic organisms The compound may build up in water-dwelling organisms, posing a risk to the environment.

Handling precautions

Should be handled with care Due to its potential health and environmental risks, proper safety measures should be taken when working with this compound.

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 103-82-2 phenylacetic acid 
• 599-67-7 1,1-diphenylethanol 
• 60-12-8 2-phenylethanol 
• 104-88-1 4-chlorobenzaldehyde 
• 104-94-9 4-methoxy-aniline 
• 881-67-4 4-nitrobenzaldehyde dimethyl acetal 

Downstream Products

• 51226-12-1 2-(3'-aminophenyl)-5,5-dimethyl-1,3-dioxane 
• 41159-02-8 2-(4-nitrophenyl)-1,3-dithiolane 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 101420-88-6 4-iodo-3-nitrobenzaldehyde 
• 949162-01-0 (S)-3-[3'-tert-butoxycarbonylamino-4'-iodo-(E)-cinnamoyl]-4-phenyloxazolidin-2-one 
• 949161-92-6 (S)-3-[3'-amino-4'-iodo-(E)-cinnamoyl]-4-phenyloxazolidin-2-one 
• 949162-00-9 (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid 
• 949161-98-2 methyl (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamate 
• 949161-94-8 methyl (E)-3'-nitro-4'-iodocinnamate 
• 949161-95-9 methyl (E)-3'-amino-4'-iodocinnamate 
• 949161-93-7 2-(4-iodo-phenyl)-5,5-dimethyl-[1,3]dioxane 
• 107708-70-3 4-(4,4-dimethyl-2,6-dioxacyclohexyl)aniline 
• 555-16-8 4-nitrobenzaldehdye 

Relevant articles and documents

Four acid-catalysed dehydration reactions proceed without interference

Four acid-catalysed dehydration reactions can proceed in one pot, simultaneously and without interference, to yield one imine, one acetal (or boronic ester), one ester and one alkene, even though many other cross-products could be conceived. This advanced

Synthesis of novel solid acidic ionic liquid polymer and its catalytic activities

The novel solid acidic ionic liquid polymer has been synthesized through the copolymerization of acidic ionic liquid oligomers and resorcinol- formaldehyde (RF resin). The catalytic activities were investigated through the acetalization. The results showed that the PIL was very efficient for the reactions with the average yield over 99.0%. The procedure was quite simple with just one-step to complete both the reactions. The high hydrophobic BET surface, high catalytic activities and high stability gave the PIL great potential for green chemical processes. Pleiades Publishing, Ltd., 2013.

Utilization of photoinduced charge-separated state of donor-acceptor-linked molecules for regulation of cell membrane potential and ion transport

The control of ion transport across cell membranes by light is an attractive strategy that allows targeted, fast control of precisely defined events in the biological membrane. Here we report a novel general strategy for the control of membrane potential