Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7533-05-3

1-Benzoylaminocyclopentanecarboxylic acid methyl ester is a complex organic compound with the molecular formula C14H17NO3. It is a derivative of cyclopentane, featuring a benzoyl group (C6H5-CO-) attached to the nitrogen atom of an amino group, and a carboxylic acid group (-COOH). The methyl ester functional group (-COOCH3) is present, indicating that the carboxylic acid has been esterified with methanol. 1-benzoylaminocyclopentanecarboxylicacid methyl ester is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the dopamine D2 receptor, due to its structural similarity to certain psychoactive substances. It is important to note that while it shares structural elements with drugs of abuse, it is not itself a drug and its effects and uses are distinct. The compound is typically synthesized in a laboratory setting and is not found naturally.

7533-05-3

Post Buying Request

7533-05-3 Suppliers

Recommended suppliersmore

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

7533-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7533-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7533-05:
(6*7)+(5*5)+(4*3)+(3*3)+(2*0)+(1*5)=93
93 % 10 = 3
So 7533-05-3 is a valid CAS Registry Number.

7533-05-3Relevant articles and documents

A facile and rapid preparation of hydroxamic acids by hydroxylaminolysis using DBU as base

Beillard, Audrey,Bhurruth-Alcor, Yushma,Bouix-Peter, Claire,Bouquet, Karinne,Chambon, Sandrine,Clary, Laurence,Harris, Craig S.,Millois, Corinne,Mouis, Grégoire,Ouvry, Gilles,Pierre, Romain,Reitz, Arnaud,Tomas, Loic

, p. 2165 - 2170 (2016)

While there are many protocols for the preparation of hydroxamic acids from their corresponding carboxylic acid or carboxylic ester precursors, most use strong mineral bases that can lead to carboxylic acid impurities that can be difficult to remove using standard chromatographic techniques. This problem is exacerbated when the carbonyl group is hindered. Herein, we communicate a robust hydroxylaminolysis protocol for the preparation of hydroxamic acids in high yield and purity.

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

What can I do for you?
Get Best Price

Get Best Price for 7533-05-3