313228-48-7

Basic information

• Product Name: 1,2-Benzenedicarbonitrile, 4-formyl- (9CI)
• Synonyms: 1,2-Benzenedicarbonitrile, 4-formyl- (9CI)
• CAS NO: 313228-48-7
• Molecular Formula: C₉H₄N₂O
• Molecular Weight: 156.14086
• Product Categories: ALDEHYDE
• Mol File: 313228-48-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 335.28 °C at 760 mmHg
• Flash Point: 156.572 °C
• Appearance: /
• Density: 1.265 g/cm³
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1,2-Benzenedicarbonitrile, 4-formyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 4-formyl- (9CI)(313228-48-7)
• EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 4-formyl- (9CI)(313228-48-7)

Safety Data

• Hazardous Substances Data: 313228-48-7(Hazardous Substances Data)

Usage

General Description

1,2-Benzenedicarbonitrile, 4-formyl- (9CI) is a chemical compound with the molecular formula C9H5NO2. It is also known as 4-formylphthalonitrile and is classified as an aromatic aldehyde. 1,2-Benzenedicarbonitrile, 4-formyl- (9CI) is used in organic synthesis and is commonly employed in the production of various dyes, pigments, and pharmaceuticals. It possesses a distinctive aromatic odor and is a white to yellow crystalline solid at room temperature. 1,2-Benzenedicarbonitrile, 4-formyl- (9CI) is also considered to be a potential irritant to the skin, eyes, and respiratory system and should be handled with caution in a laboratory setting.

Upstream product

• 150457-71-9 4-Vinylphthalonitrile 
• 74003-55-7 3,4-dibromobenzaldehyde 
• 544-92-3 copper(I) cyanide 
• 69518-17-8 4-iodo-1,2-dicyanobenzene 
• 63089-50-9 4-methylphthalonitrile 

Downstream Products

• 60469-86-5 3,4-dicyano benzoic acid 
• 437552-35-7 3,4-dicyanobezoyl chloride 
• 210037-82-4 4-hydroxymethyl-1,2-dicyanobenzene 

Relevant articles and documents

Postfunctionalization of helical polyisocyanopeptides with phthalocyanine chromophores by "click chemistry"

Rigid rod polyisocyanopeptides bearing phthalocyanines as pendant groups have been synthesised through CuAAC of polyisocyanopeptides containing acetylene groups with zinc(II) phthalocyanine azide. As confirmed by UV/Vis, fluorescence, and circular dichroi

Synthesis and characterization of peripherally ferrocene-modified zinc phthalocyanine for dye-sensitized solar cell

Synthesis and structural characterization of peripherally ferrocene-substituted zinc phthalocyanine (ZnPc-Fc) werecarried out for efficient far-red/near-IR performance in dye-sensitized nanostructured TiO 2 solar cells. Incorporating ferrocene

Synthesis and electrochemical properties of phthalocyanine - Fullerene hybrids

Phthalocyanines linked to C60 have been synthesized by two general strategies. One of them involves the addition of an azomethine ylide prepared in situ from a formyl phthalocyanine to C60, and the other one involves a statistical co