Welcome to LookChem.com Sign In|Join Free
  • or
1H-Pyrrole-2-carboxylic acid, 4-ethyl-3-methyl-5-propyl, ethyl ester is a complex organic compound with the chemical formula C14H23NO2. It is a derivative of pyrrole-2-carboxylic acid, featuring an ethyl ester group attached to the carboxylic acid moiety. The molecule is characterized by the presence of a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom. The substituents on the pyrrole ring include an ethyl group at position 4, a methyl group at position 3, and a propyl group at position 5. 1H-Pyrrole-2-carboxylic acid, 4-ethyl-3-methyl-5-propyl-, ethyl ester is an ester, with the ethyl group from the ester functionality extending from the carboxylic acid group. It is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity.

4962-78-1

Post Buying Request

4962-78-1 Suppliers

Recommended suppliers

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

4962-78-1 Usage

Structure

1H-Pyrrole-2-carboxylic acid, 4-ethyl-3-methyl-5-propyl-, ethyl ester

Appearance

Clear, colorless to pale yellow liquid

Solubility

Soluble in organic solvents such as ethanol and acetone

Use

Building block for the synthesis of various compounds in pharmaceutical and chemical research

Known for

Used in the development of pharmaceuticals and agrochemicals due to its structural properties and potential biological activity

Check Digit Verification of cas no

The CAS Registry Mumber 4962-78-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4962-78:
(6*4)+(5*9)+(4*6)+(3*2)+(2*7)+(1*8)=121
121 % 10 = 1
So 4962-78-1 is a valid CAS Registry Number.

4962-78-1Downstream Products

4962-78-1Relevant academic research and scientific papers

Regioselective pyrrole synthesis from asymmetric β-diketone and conversion to sterically hindered porphyrin

Fujii, Hiroshi,Yoshimura, Tetsuhiko,Kamada, Hitoshi

, p. 1427 - 1430 (1997)

The condensation of asymmetric β-diketones with α-oximinoacetoacetate esters affords pyrroles regioselectively. The mechanism of the regioselectivity is studied using 13C-NMR spectroscopy. Pyrrole having a neopentyl group at the 4-position is synthesized by the method, and further converted to a steric hindered porphyrin in good yield.

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 4962-78-1