Welcome to LookChem.com Sign In|Join Free
  • or
1,2-Ethanediol, 2-(4-methoxyphenyl)-1,1-diphenyl- is a complex organic compound with the molecular formula C17H18O3. It is a derivative of ethylene glycol, featuring a 4-methoxyphenyl group attached to the second carbon atom, and two phenyl groups bonded to the first carbon atom. 1,2-Ethanediol, 2-(4-methoxyphenyl)-1,1-diphenyl- is characterized by its unique structure, which combines the properties of an ether, an alcohol, and an aromatic ring. It is a colorless to pale yellow liquid with a specific molecular weight of 274.32 g/mol. Due to its chemical structure, it exhibits various properties such as solubility in organic solvents and potential reactivity with electrophiles. 1,2-Ethanediol, 2-(4-methoxyphenyl)-1,1-diphenyl- may have applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals, where its unique structure can contribute to specific reactivity or physical properties.

4237-52-9

Post Buying Request

4237-52-9 Suppliers

Recommended suppliers

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

4237-52-9 Usage

Chemical structure

Diphenyl ether derivative with a 4-methoxyphenyl group attached to the 2-position of the 1,2-ethanediol backbone

Applications

Commonly used in the synthesis of organic compounds and pharmaceuticals

Potential uses

Drug development and material science

Reactivity

Unique structure and reactivity due to its chemical composition

Further research

May reveal additional benefits and uses for 1,2-Ethanediol, 2-(4-methoxyphenyl)-1,1-diphenyl-

Check Digit Verification of cas no

The CAS Registry Mumber 4237-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4237-52:
(6*4)+(5*2)+(4*3)+(3*7)+(2*5)+(1*2)=79
79 % 10 = 9
So 4237-52-9 is a valid CAS Registry Number.

4237-52-9Relevant academic research and scientific papers

Reductive coupling between aromatic aldehydes and ketones or imines by copper catalysis

Takeda, Mitsutaka,Mitsui, Atsuhisa,Nagao, Kazunori,Ohmiya, Hirohisa

, p. 3664 - 3669 (2019)

The copper-catalyzed reductive coupling of two different carbonyl compounds has been achieved. The reaction of aromatic aldehydes and arylketones with a silylboronate in the presence of a catalytic amount of a CuCl-N-heterocyclic carbene (NHC) complex and a stoichiometric amount of alkoxide base yielded cross-coupled 1,2-diol derivatives. A reaction pathway is proposed that involves the catalytic formation of a nucleophilic α-silyloxybenzylcopper(I) species from the aromatic aldehyde and its subsequent coupling with the arylketone. This process was amenable to asymmetric catalysis. This copper catalyst system also enabled the reductive coupling between aromatic aldehydes and imines.

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 4237-52-9