52033-96-2 Usage
Chemical Class
Fluoroaryl amines
Molecular Weight
128.14 g/mol
Appearance
Colorless to light yellow solid or liquid
Melting Point
54-57°C
Boiling Point
346°C
Density
1.3 g/cm3
Solubility
Soluble in water, ethanol, and acetone
Reactivity
Can react with acids, oxidizing agents, and reducing agents
Uses
Manufacturing of polymers
Production of dyes
Synthesis of pharmaceuticals
Raw material for aramid fibers (high-strength, heat-resistant materials)
Industrial Applications
Production of adhesives
Coatings
Specialty chemicals
Safety Precautions
Causes skin, eye, and respiratory irritation
Harmful if ingested or inhaled
Handle with care and use appropriate protective equipment
Storage
Store in a cool, dry, and well-ventilated area, away from incompatible substances
Regulatory Status
May be subject to specific regulations depending on the region and intended use
Environmental Impact
Potentially harmful to aquatic life and should be disposed of properly according to local regulations
Synonyms
2-Fluoro-1,3-phenylenediamine, 2-Fluoro-1,3-benzenediamine, o-Phenylenediamine, 2-fluoro-
Chemical Structure
A benzene ring with two amine groups (-NH2) at the 1 and 3 positions and a fluorine atom (-F) at the 2 position.
Check Digit Verification of cas no
The CAS Registry Mumber 52033-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52033-96:
(7*5)+(6*2)+(5*0)+(4*3)+(3*3)+(2*9)+(1*6)=92
92 % 10 = 2
So 52033-96-2 is a valid CAS Registry Number.
52033-96-2Relevant articles and documents
Converting sequences of aromatic amino acid monomers into functional three-dimensional structures: Second-generation helical capsules
Bao, Chunyan,Kauffmann, Brice,Gan, Quan,Srinivas, Kolupula,Jiang, Hua,Huc, Ivan
supporting information; experimental part, p. 4153 - 4156 (2009/03/11)
New codes for sequence-structure-function relationships can be elaborated in aromatic oligoamide foldamers upon varying main-chain components. Each monomer carries its own structural and functional features and enables oligomeric sequences to be designed