Welcome to LookChem.com Sign In|Join Free
  • or
Phenol, 4-(1-methylhexyl)-, also known as 4-(1-methylhexyl)phenol or 4-sec-hexylphenol, is an organic compound with the chemical formula C??H??O. It is a derivative of phenol, where a 1-methylhexyl group is attached to the para position (4th carbon) of the phenol molecule. Phenol, 4-(1-methylhexyl)- is a colorless to pale yellow liquid with a characteristic phenolic odor. It is used as an intermediate in the synthesis of various chemicals, including antioxidants, UV stabilizers, and polymers. Due to its phenolic nature, it exhibits antioxidant properties and is also used as a stabilizer in the plastics industry to prevent degradation caused by heat, light, and oxygen. The compound is insoluble in water but soluble in organic solvents. It is important to handle this chemical with care due to its potential irritant and toxic properties.

6863-24-7

Post Buying Request

6863-24-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6863-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6863-24-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6863-24:
(6*6)+(5*8)+(4*6)+(3*3)+(2*2)+(1*4)=117
117 % 10 = 7
So 6863-24-7 is a valid CAS Registry Number.

6863-24-7Relevant 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 (1997)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6863-24-7