1005340-01-1

Basic information

• Product Name: 1,2-Diiodo-4,5-di-n-butoxybenzene
• Synonyms: 1,2-Diiodo-4,5-di-n-butoxybenzene;N-[(2S)-4-amino-1-[[(2S,3R)-1-[[(2S)-4-amino-1-oxo-1-[[(3S,6S,9S,12S,15R,18S,21S)-6,9,18-tris(2-aminoethyl)-3-[(1S)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]amino]butan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxobutan-2-yl]-5-methylheptanamide
• CAS NO: 1005340-01-1
• Molecular Formula: C₁₄H₂₀I₂O₂
• Molecular Weight: 474.11634
• Product Categories: organic compound
• Mol File: 1005340-01-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 423.8±45.0 °C(Predicted)
• Appearance: white to yellow/Powder
• Density: 1.689±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,2-Diiodo-4,5-di-n-butoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Diiodo-4,5-di-n-butoxybenzene(1005340-01-1)
• EPA Substance Registry System: 1,2-Diiodo-4,5-di-n-butoxybenzene(1005340-01-1)

Safety Data

• Hazardous Substances Data: 1005340-01-1(Hazardous Substances Data)

Usage

Chemical structure

A benzene ring with two iodine atoms at positions 1 and 2, and two n-butoxy groups at positions 4 and 5.

Usage

Primarily used as a reagent in organic synthesis and as a versatile intermediate in chemical reactions.

Physical state

A clear, colorless to pale yellow liquid.

Solubility

Insoluble in water, but soluble in organic solvents such as ethanol and ether.

Applications

Used in the pharmaceutical and agrochemical industries, as well as in the manufacture of dyes and pigments.

Hazards

Potential for skin and eye irritation, and should be handled with care.

Upstream product

• 120-80-9 benzene-1,2-diol 
• 20367-35-5 1,2-dibutoxybenzene 

Downstream Products

• 1031223-84-3 C₅₀H₆₈N₂O₂Si₂ 
• 1031225-94-1 C₃₂H₄₄INO₂Si 
• 1463472-77-6 C₃₂H₂₈N₂O₆S₈ 
• 1463472-76-5 C₃₆H₃₄O₆S₈ 
• 1337988-56-3 1,2-dibutoxy-4,5-bis[(trimethylsilyl)ethynyl]benzene 

Relevant articles and documents

Synthesis, optical and electrochemical properties of novel D-π-A type conjugated polymers based on benzo[c][1,2,5]selenadiazole unit via alkyne module

Three novel donor-π-acceptor (D-π-A) type conjugated polymers P-1, P-2, and P-3 based on benzo[c][1,2,5]selenadiazole moiety and phenyl or naphthyl group via alkyne module were firstly prepared by Sonogashira-Hagihara reaction of various diiodo aryl compounds with the key monomer 4,7-diethynylbenzo[c] [1,2,5]selenadiazole (M-1), which was synthesized by a strategy of firstly introducing the trimethylsilylacetylene flexible group, and then introducing the selenium atom. The polymers displayed obvious absorption peaks at the region from 503 to 510 nm and narrow orange-red or red fluorescence in the range of 576-595 nm because benzo[c][1,2,5]selenadiazole unit can effectively reduce the lowest unoccupied molecular orbital (LUMO) energy levels of these polymers. The band gaps of these polymers can be tuned in the range of 1.37-1.76 eV by using different aryl donor groups. These findings indicate that these benzo[c][1,2,5]selenadiazole-based conjugated polymers can be developed for excellent fluorescent materials.

Synthesis, spectroscopy, and theoretical calculations for a series of push-pull [14]-pyridoannulenes

(Chemical Equation Presented) Three new isomeric dipyridoannulenes were synthesized and characterized. These molecules possess differing conjugation pathways between the substituent alkoxy donating groups and the pyridyl acceptor groups. Optical absorptio