111373-32-1

Basic information

• Product Name: Benzenepropanal, 2-iodo-
• Synonyms: Benzenepropanal, 2-iodo-;3-(2-iodophenyl)propanal
• CAS NO: 111373-32-1
• Molecular Formula: C₉H₉IO
• Molecular Weight: 260.07163
• Mol File: 111373-32-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 287.738°C at 760 mmHg
• Flash Point: 127.819°C
• Appearance: /
• Density: 1.644g/cm³
• Vapor Pressure: 0.002mmHg at 25°C
• Refractive Index: 1.592
• CAS DataBase Reference: Benzenepropanal, 2-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanal, 2-iodo-(111373-32-1)
• EPA Substance Registry System: Benzenepropanal, 2-iodo-(111373-32-1)

Safety Data

• Hazardous Substances Data: 111373-32-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H9IO/c10-9-6-2-1-4-8(9)5-3-7-11/h1-2,4,6-7H,3,5H2

Upstream product

• 615-42-9 1,2-Diiodobenzene 
• 107-18-6 allyl alcohol 
• 412272-54-9 ethyl 3-(2-iodophenyl)acrylate 
• 59473-45-9 2-(chloromethyl)iodobenzene 
• 26260-02-6 2-iodobenzaldehyde 
• 26059-41-6 3-(2-iodophenyl)-1-propanol 
• 40888-21-9 methyl (E)-3-(2′-iodophenyl)acrylate 
• 5159-41-1 2-iodobenzyl alcohol 

Downstream Products

• 111373-33-2 3-[1-Hydroxy-3-(2-iodo-phenyl)-propyl]-3H-isobenzofuran-1-one 
• 68253-35-0 (E)-indan-1-one oxime 
• 1459793-09-9 (S)-N-[3-(2-iodophenyl)propylidene]-2,4,6-trimethylbenzenesulfinamide 
• 1459793-08-8 (S)-N-(3-(2-iodophenyl)propylidene)-2-methylpropane-2-sulfinamide 
• 1271193-05-5 2-(3-(2-iodophenyl)propyl)-3-oxocyclohex-1-enyl trifluoromethanesulfonate 
• 111373-38-7 Methanesulfonic acid 3-(2-iodo-phenyl)-1-(3-oxo-1,3-dihydro-isobenzofuran-1-yl)-propyl ester 
• 111373-35-4 2-[2-(2-Iodo-phenyl)-ethyl]-indan-1,3-dione 
• 111373-34-3 3-[3-(2-Iodo-phenyl)-prop-(Z)-ylidene]-3H-isobenzofuran-1-one 
• 188990-05-8 2-{tert-Butoxycarbonyl-[3-(2-iodo-phenyl)-propyl]-amino}-acrylic acid methyl ester 
• 188990-11-6 N-<3-(2-Iodophenyl)propyl>serine methyl ester 

Relevant articles and documents

Intramolecular Cycloaddition Approach to Fused Pyrazoles: Access to 4,5-Dihydro-2 H -pyrazolo[4,3- c ]quinolines, 2,8-Dihydroindeno[2,1- c ]pyrazoles, and 4,5-Dihydro-2 H -benzo[ e ]indazoles

A straightforward and efficient method for the synthesis of pyrazoles fused with 1,2,3,4-tetrahydroquinoline, 2,3-dihydro-1 H -indene, or 1,2,3,4-tetrahydronaphthalene involves the formation of the tosylhydrazone from an aromatic substrate carrying aldehy

Highly diastereoselective radical cyclisations of chiral sulfinimines

Chiral amines are formed by the highly diastereoselective intramolecular addition of alkyl and aryl radicals onto chiral mesityl sulfinimines.

Intramolecular [1 + 2] and [3 + 2] cycloaddition reactions of cyclopropenone ketals

The first intramolecular thermal reactions of cyclopropenone ketals are reported and the work examined substrates tethered to an electron-deficient olefin bearing a single electron-withdrawing substituent. Whereas the intermolecular variants of the reacti