246530-08-5

Basic information

• Product Name: 2-Propenal, 3-(2-broMophenyl)-2-Methyl-
• Synonyms: 2-Propenal, 3-(2-broMophenyl)-2-Methyl-
• CAS NO: 246530-08-5
• Molecular Formula: C10H9BrO
• Molecular Weight: 225.08186
• Mol File: 246530-08-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propenal, 3-(2-broMophenyl)-2-Methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-(2-broMophenyl)-2-Methyl-(246530-08-5)
• EPA Substance Registry System: 2-Propenal, 3-(2-broMophenyl)-2-Methyl-(246530-08-5)

Safety Data

• Hazardous Substances Data: 246530-08-5(Hazardous Substances Data)

Usage

General Description

2-Propenal, 3-(2-broMophenyl)-2-Methyl- is a chemical compound that contains a propenal group and a 2-bromophenyl group attached to a methyl group. It is a highly reactive compound that is commonly used in the production of various organic compounds, including pharmaceuticals, agrochemicals, and polymers. The presence of the 2-bromophenyl group gives the compound additional reactivity and makes it useful in a wide range of chemical reactions. Due to its reactive nature and potential health hazards, proper safety precautions must be taken when handling and using this compound.

Upstream product

• 123-38-6 propionaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 1428319-13-4 (E)-3-(2-bromophenyl)-1-(3,4-dihydro-2H-pyran-6-yl)-2-methylprop-2-en-1-ol 
• 1428319-25-8 (E)-3-(2-bromophenyl)-1-(3,4-dihydro-2H-pyran-6-yl)-2-methylprop-2-en-1-one 
• 1428319-39-4 (5S,6R)-5-(2-bromophenyl)-6-methyl-3,4,5,6-tetrahydrocyclopenta[b]pyran-7(2H)-one 
• 1428319-58-7 (5S,6S)-5-(2-bromophenyl)-6-methyl-3,4,5,6-tetrahydrocyclopenta[b]pyran-7(2H)-one 
• 1311148-19-2 (2E,4E)-5-(2-bromophenyl)-2-methoxy-4-methylpenta-2,4-dien-1-ol 

Relevant articles and documents

Process for the Preparation of Idnanones

A process of forming compounds of formula I comprising the steps of addition of an amino compound H2NR to a compound of formula (II) followed by cyclization, isomerization and hydrolysis.

Concise total synthesis of (±)-cephalotaxine via a transannulation strategy: Development of a facile reductive oxy-Nazarov cyclization

A concise total synthesis of (±)-cephalotaxine (1) has been achieved from dioxolanone derivative 15 via a transannulation strategy. The key transformation is a facile reductive oxy-Nazarov cyclization as illustrated above, involving presumably a tethered 1,2-oxidopentadienyl cation species 7a or 7b, which represents a new variant of the oxy-Nazarov cyclization and constitutes an effective, regio- and stereospecific 5-hydroxy cyclopentenone annulation protocol under mild hydride reduction conditions.