6280-98-4

Basic information

• Product Name: 1,2-DI-N-PROPOXYBENZENE
• Synonyms: 1,2-DI-N-PROPOXYBENZENE;CATECHOL DI-N-PROPYL ETHER;PYROCATECHOL DI-N-PROPYL ETHER;1,2-DIPROPOXYBENZENE;Catechol Dipropyl Ether;Pyrocatechol Dipropyl Ether;o-Dipropoxybenzene
• CAS NO: 6280-98-4
• Molecular Formula: C₁₂H₁₈O₂
• Molecular Weight: 194.27
• Mol File: 6280-98-4.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 118 °C / 21mmHg
• Flash Point: 74.1 °C
• Appearance: /
• Density: 0.98
• Refractive Index: 1.4950 (estimate)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2-DI-N-PROPOXYBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DI-N-PROPOXYBENZENE(6280-98-4)
• EPA Substance Registry System: 1,2-DI-N-PROPOXYBENZENE(6280-98-4)

Safety Data

• Hazardous Substances Data: 6280-98-4(Hazardous Substances Data)

Usage

General Description

1,2-Di-N-Propoxybenzene, also known as 1,2- bis(propoxy)benzene, is a chemical compound with the molecular formula C12H16O2. It is distinguished by two propoxy functional groups (-OCH2CH2CH3) attached to a benzene ring. The compound is categorized under aromatic ethers and is widely used for industrial and chemical synthesis applications. Details about its physical properties, such as its melting and boiling points, toxicity, or specific industrial applications, are not readily available in the public domain; thus, one needs to handle it with care until comprehensive safety data is available.

Upstream product

• 120-80-9 benzene-1,2-diol 
• 4218-87-5 1,2-bis-allyloxy-benzene 
• 106-94-5 propyl bromide 

Downstream Products

• 123769-54-0 (E)-1-(3,4-Dipropoxy-phenyl)-3-phenyl-propenone 
• 118464-38-3 1,2-dibromo-4,5-dipropyloxybenzene 
• 161199-97-9 1,2-dipropoxy-4-(3-dimethylaminopropionyl)benzene 
• 86723-15-1 1,2-dipropyloxy-4,5-diaminobenzene 
• 50766-19-3 1,6-Bis-(3,4-dipropoxyphenyl)-1,6-hexandion 
• 33332-61-5 1,2-dipropoxy-4,5-dinitrobenzene 
• 91645-47-5 4-Nitro-1,2-dipropoxy-benzene 
• 123769-53-9 (3,4-Dipropoxy-phenyl)-phenyl-methanone 
• 127119-34-0 4-propionyl-1,2-dipropoxybenzene 
• 85417-84-1 4-bromo-1,2-bis(propoxy)benzene 
• 100620-61-9 4-chloromethyl-1,2-dipropoxy-benzene 
• 105321-59-3 1,2-dipropoxy-4-acetylbenzene 
• 101114-73-2 3,4-dipropoxy-benzyl thiocyanate 
• 69769-43-3 (3,4-dipropoxy-phenyl)-acetonitrile 

Relevant articles and documents

Synthesis of Armchair and Chiral Carbon Nanobelts

Carbon nanobelts that consist of a loop of fully fused benzene rings are long-standing and challenging targets of organic synthesis and are key steps toward the ultimate synthesis of uniform carbon nanotubes (CNTs) of single chirality and predefined diame

METHODS AND COMPOSITIONS FOR CONTROL OF GYPSY MOTHS, Lymanria dispar

The invention provides in part dialkoxybenzene and eugenol compounds for controlling infestation by a Lymantria dispar, and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; with the provisos that when R2 is at position 2, R3 if present is at position 3, or when R2 is at to position 3, R3 if present is at positions 2 or 4, or when R2 is at position 4, R3 if present is at position 2; or of Formula II: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; or mixtures thereof.

Photophysical and photochemical properties of fluorinated and nonfluorinated n-Propanol-substituted zinc phthalocyanines

The synthesis of symmetrical fluorinated and nonfluorinated zinc(II) phthalocyanine derivatives obtained from. 4,5-dichlorophthalonitrile, 4-nitrophthalonitrile and 3-nitrophthalonitrile substituted with 2,2,3,3-tetrafluoro-1-propanol and npropanol are de