1577-33-9 Usage
Functional groups
Chlorine atom bonded to a phenyl group
Methyl group bonded to a pentene chain
Carbonyl group (C=O)
Structure
4-chlorophenyl group attached to a 4-methylpent-1-en-3-one backbone
Reactivity
Versatile reactivity due to the presence of multiple functional groups
Can undergo various organic reactions such as nucleophilic substitution, electrophilic aromatic substitution, and Michael addition
Applications
Used in organic synthesis and pharmaceutical research
Key intermediate in the synthesis of various pharmaceuticals and natural products
Starting material for the preparation of other important chemical compounds
Biological activity
Potential biological activity due to its structural features
Can be further modified or functionalized to enhance its biological properties
Physical state
Likely a liquid or solid at room temperature, depending on the specific conditions
Solubility
Soluble in organic solvents such as ethanol, acetone, and dichloromethane
Insoluble in water due to the presence of nonpolar functional groups
Stability
Generally stable under normal conditions, but may be sensitive to heat, light, or strong bases/acids
Can undergo degradation or side reactions if not stored or handled properly
Check Digit Verification of cas no
The CAS Registry Mumber 1577-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1577-33:
(6*1)+(5*5)+(4*7)+(3*7)+(2*3)+(1*3)=89
89 % 10 = 9
So 1577-33-9 is a valid CAS Registry Number.
1577-33-9Relevant articles and documents
Synthesis of Polysubstituted Pyridines via a One-Pot Metal-Free Strategy
Wei, Hongbo,Li, Yun,Xiao, Ke,Cheng, Bin,Wang, Huifei,Hu, Lin,Zhai, Hongbin
, p. 5974 - 5977 (2016/01/09)
An efficient strategy for the one-pot synthesis of polysubstituted pyridines via a cascade reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction sequence involves a Wittig reaction, a Staudinger reaction, an aza-Wittig reaction, a 6π-3-azatriene electrocyclization, and a 1,3-H shift. This protocol provides quick access to the polysubstituted pyridines from readily available substrates in good to excellent yields.
