Welcome to LookChem.com Sign In|Join Free
  • or
1H-Imidazole-2-sulfonic acid, 4-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1-ethenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96439-71-3

Post Buying Request

96439-71-3 Suppliers

Recommended suppliers

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

96439-71-3 Usage

Imidazole ring

A five-membered heterocyclic ring with four carbon atoms and one nitrogen atom, which is a common structural motif in many biologically active compounds.

Sulfonic acid group

A functional group consisting of a sulfur atom bonded to an oxygen atom and a hydrogen atom (-SO2H), which can impart acidity and may be involved in hydrogen bonding and electrostatic interactions.

Ethenyl group

A vinyl group (-CH=CH2) attached to the compound, which can participate in various organic reactions such as addition, polymerization, and oxidation.

4-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl] moiety

A phenyl ring (a six-membered carbon ring with alternating single and double bonds) substituted with two tert-butyl groups (C(CH3)3) at the 3 and 5 positions, and a hydroxy group (-OH) at the 4 position. This moiety can be responsible for various pharmacological activities and may contribute to the compound's solubility and stability.

Tert-butyl groups

Two bulky, electron-donating groups (C(CH3)3) attached to the phenyl ring, which can influence the compound's steric properties, reactivity, and solubility.

Hydroxy group

A polar, hydrophilic functional group (-OH) attached to the phenyl ring, which can participate in hydrogen bonding and may affect the compound's solubility and stability in aqueous environments.

Potential pharmaceutical applications

Due to the presence of imidazole derivatives and phenolic compounds, 1H-Imidazole-2-sulfonic acid, 4-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1-ethenyl- may have potential uses in pharmaceuticals, such as antifungal, antiviral, or anti-inflammatory agents.

Potential catalytic or synthetic applications

The presence of the sulfonic acid group may indicate its potential use as a catalyst or as a reagent in organic synthesis, although further research and testing would be necessary to determine its specific applications and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 96439-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96439-71:
(7*9)+(6*6)+(5*4)+(4*3)+(3*9)+(2*7)+(1*1)=173
173 % 10 = 3
So 96439-71-3 is a valid CAS Registry Number.

96439-71-3Downstream Products

96439-71-3Relevant academic research and scientific papers

Studies on the synthesis and anti-inflammatory activity of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position. V.1) Elimination reaction of the sulfinyl group of 2,3-dihydroimidazo[2,1-b]thiazole 1-oxide

Isomura,Kubo

, p. 4726 - 4630 (2007/10/02)

Reaction of 6-(3,5-di-tert-butyl-4-hydroxyphenyl)-2,3-dihydroimidazo[2,1-b]thiazole 1-oxide (1) with superoxide anion gave 4-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-vinylimidazole (2). Compound 2 was also obtained by treatment of 1 with potassium tert-butox

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 96439-71-3