6465-71-0 Usage
Uses
Used in Chemical Synthesis Industry:
Phenol, 4-(1-propylbutyl)is used as an intermediate in the production of antioxidants, which are essential in preventing the oxidation of materials and extending their shelf life. Its presence in the synthesis process contributes to the development of various chemical products.
Used in Pharmaceutical Industry:
As an intermediate, Phenol, 4-(1-propylbutyl)plays a crucial role in the development of pharmaceuticals. Its unique structure allows it to be a building block for creating new drugs, potentially leading to advancements in medicine.
Used in Fragrance Industry:
Phenol, 4-(1-propylbutyl)is used as a component in the creation of fragrances. Its aromatic properties make it suitable for use in perfumes and other scented products, enhancing the sensory experience of consumers.
Used in Plastics Industry:
This chemical compound serves as a stabilizer in plastics, helping to prevent degradation and maintain the integrity of plastic materials. Its use in this industry contributes to the durability and longevity of plastic products.
Used in Lubricants Industry:
Phenol, 4-(1-propylbutyl)is also a component in specialty lubricants, where it contributes to the performance and efficiency of these products. Its presence in lubricants can improve their stability and effectiveness in various applications.
However, it is important to note that 4-tert-butylphenol has been identified as a potential endocrine disruptor, leading to restrictions or bans in certain consumer products. This highlights the need for careful consideration of its use and potential health and environmental implications.
Check Digit Verification of cas no
The CAS Registry Mumber 6465-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6465-71:
(6*6)+(5*4)+(4*6)+(3*5)+(2*7)+(1*1)=110
110 % 10 = 0
So 6465-71-0 is a valid CAS Registry Number.
6465-71-0Relevant academic research and scientific papers
Metal cation-exchanged montmorillonite (Mn+-mont)-catalysed aromatic alkylation with aldehydes and ketones
Tateiwa, Jun-Ichi,Hayama, Ei,Nishimura, Takahiro,Uemura, Sakae
, p. 1923 - 1928 (2007/10/03)
The alkylation of aromatic compounds with aldehydes and ketones in the presence of a variety of metal cation-exchanged montmorillonites (Mn+-mont; Mn+ = Zr4+, Al3+, Fe3+, Zn2+, H+, Na+) has been investigated. Al3+- and Zr4+-Monts are revealed to be effective as catalysts, while no reaction takes place with Na+-mont. Al3+-Mont-catalysed alkylation of phenol with several aldehydes produces mainly or almost solely the corresponding gem-bis(hydroxyphenyl)alkanes (bisphenols) in good yields, while that with several ketones affords selectively the corresponding alkylphenols in moderate to good yields. The alkylation always occurs at the carbonyl carbon without any skeletal rearrangement and the kind of products depends much on the steric hindrance of an electrophilic intermediary carbocation. The alkylation of anisole, veratrole and p-cresol proceeds well, while that of toluene, benzene, chlorobenzene and nitrobenzene scarcely occurs.
