5694-69-9 Usage
Uses
Used in Pharmaceutical Industry:
Phenyl(2-phenyl-1,3-dioxolan-2-yl)methanol is utilized as a precursor in the production of various drugs. Its unique molecular structure allows for the creation of complex pharmaceutical compounds, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, phenyl(2-phenyl-1,3-dioxolan-2-yl)methanol is employed as a starting material for the synthesis of pesticides. Its chemical properties make it suitable for the formulation of effective crop protection products.
Safety Considerations:
It is crucial to handle phenyl(2-phenyl-1,3-dioxolan-2-yl)methanol with care due to its potential health and environmental risks. Proper management and safety measures are essential to mitigate any adverse effects associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5694-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5694-69:
(6*5)+(5*6)+(4*9)+(3*4)+(2*6)+(1*9)=129
129 % 10 = 9
So 5694-69-9 is a valid CAS Registry Number.
5694-69-9Relevant academic research and scientific papers
Synthesis of 9,10-phenanthrenequinones by photocyclization of derivatives of benzoins: Scope and limitation of the methodology
Togashi, Denisio Masaharu,Nicodem, David Ernest,Marchiori, Roberto,Marchiori, Maria Luisa P. De F. C.
, p. 1051 - 1063 (2007/10/03)
Symmetric 9,10-phenanthrenequinones with methyl, methoxy, and chloro substituents at the 3 and 6 positions have been synthesized by photocyclization of 4,5-bis-(aryl)-2-phenyl-1,3,2-dioxaboroles and 2,3- diarydioxenes followed by oxidative hydrolysis.
Reactions of α-Hydroxy Carbonyl Compounds with Azodicarboxylates and Triphenylphosphine: Synthesis of α-N-Hydroxy Amino Acid Derivatives
Kolasa, Teodozyj,Miller, Marvin J.
, p. 4978 - 4984 (2007/10/02)
Reaction of aliphatic α-hydroxy esters with azodicarboxylates and triphenylphosphine in the presence of either CbzNHOCH2Ph or trOCNHOCH2Ph provides a direct route to protected α-N-hydroxy amino acids.Similar reactions with aromatic α-hydroxy carbonyl compounds and derivatives result in predominate oxidation to the corresponding α-oxo carbonyl derivatives.
