67565-47-3 Usage
Appearance
Yellow crystalline substance A solid with a yellow color and a crystalline structure.
Molecular weight
259.27 g/mol The mass of one mole of the compound, which is 259.27 grams.
Usage in organic synthesis
Building block for various pharmaceuticals and biologically active compounds It serves as a starting material or intermediate in the synthesis of different organic compounds, including drugs and other biologically relevant molecules.
Usage in agrochemicals and dyes
Reagent in production It is used as a chemical reagent in the manufacturing process of agricultural chemicals and dyes.
Usage in fragrance and flavor compounds
Manufacturing The compound is involved in the production of fragrances and flavor compounds for various applications.
Potential toxicity and health hazards
Handle with care and proper safety procedures Due to possible harmful effects, it is important to follow safety guidelines and precautions when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 67565-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,6 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67565-47:
(7*6)+(6*7)+(5*5)+(4*6)+(3*5)+(2*4)+(1*7)=163
163 % 10 = 3
So 67565-47-3 is a valid CAS Registry Number.
67565-47-3Relevant articles and documents
Cesium fluoride-Celite: A solid base for efficient syntheses of aromatic esters and ethers
Shah, Syed Tasadaque Ali,Khan, Khalid Mohammed,Hussain, Hidayat,Anwar, Muhammad Usman,Fecker, Miriam,Voelter, Wolfgang
, p. 6652 - 6656 (2007/10/03)
Coupling reactions of a number of aromatic and heteroaromatic phenols with alkyl, acyl or benzoyl halides in acetonitrile with cesium fluoride-Celite are described, demonstrating that this reagent provides an efficient, convenient and practical method for the syntheses of aromatic esters and ethers.
Electron Apportionment in Cleavage of Radical Anions. 1. Nitro-Substituted Benzyl Phenyl Ethers
Maslak, Przemyslaw,Guthrie, Robert D.
, p. 2628 - 2636 (2007/10/02)
The radical anions of 4-nitrobenzyl phenyl ethers undergo cleavage at least 10E4 times faster than the radical anions of corresponding 4-nitrophenyl benzyl ethers despite a perceived thermodynamic advantage for the latter set of reactions.It is suggested that this results reflects a kinetic advantage for cleavage reactions which take place with regioconservation of spin density.
