Welcome to LookChem.com Sign In|Join Free
  • or
2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-4-methylpentanoic acid is a complex organic compound with the molecular formula C10H11NO4. It is characterized by a pyrrol-1-yl group attached to a 4-methylpentanoic acid chain. 2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-4-methylpentanoic acid is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its structure features a 2,5-dihydro-1H-pyrrol ring, which is fused with a 2,5-dioxo group, indicating the presence of two oxygen atoms in a cyclic structure. The 4-methylpentanoic acid part of the molecule contributes to its acidic properties, making it a carboxylic acid. The compound's unique structure and properties make it a subject of interest for researchers in medicinal chemistry, as it may play a role in the development of new therapeutic agents.

62212-18-4

Post Buying Request

62212-18-4 Suppliers

Recommended suppliers

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

62212-18-4 Usage

Derivative of amino acid

Proline

Potential use

Pharmaceutical and medicinal chemistry

Known as

Inhibitor of dipeptidyl peptidase-4 (DPP-4)

Role in the body

Regulation of blood sugar levels

Potential application

Treatment of type 2 diabetes

Investigated for

Anti-inflammatory and antioxidant properties

Check Digit Verification of cas no

The CAS Registry Mumber 62212-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62212-18:
(7*6)+(6*2)+(5*2)+(4*1)+(3*2)+(2*1)+(1*8)=84
84 % 10 = 4
So 62212-18-4 is a valid CAS Registry Number.

62212-18-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dioxopyrrol-1-yl)-4-methylpentanoic acid

1.2 Other means of identification

Product number -
Other names 2-(2,5-DIOXO-2,5-DIHYDRO-1H-PYRROL-1-YL)-4-METHYLPENTANOIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62212-18-4 SDS

62212-18-4Downstream Products

62212-18-4Relevant academic research and scientific papers

Facile preparation of poly(N-isopropylacrylamide)-based hydrogels via aqueous Diels-Alder click reaction

Wei, Hong-Liang,Yang, Zhe,Chu, Hui-Juan,Zhu, Jing,Li, Zhi-Cheng,Cui, Jin-Shi

, p. 1694 - 1702 (2010)

The study reports a facile method of preparing poly(N-isopropylacrylamide)- based hydrogels by means of the Diels-Alder reaction. First, polymeric dienes were synthesized by free radical copolymerization between N-isopropylacrylamide (NIPA) and furfuryl methacrylate (FM), with 2, 2′-azobisisobutyronitrile (AIBN) as an initiator, and polymeric dienophile was obtained by a coupling reaction of poly(ethylene glycol) (PEG) and N-maleoyl-l-leucine (LMI) under N, N′-dicyclohexylcarbodiimide (DCC). Afterwards, the resultant dienes and dienophiles were dissolved in water and put in a refrigerator remaining a temperature of 9 °C, gelation via Diels-Alder reaction was observed after some time. The samples obtained at different steps were characterized by FTIR, NMR, GPC, SEM, CD, etc. It was found that LCST of copolymers decreases with the increase of FM content in copolymers. And the disassembly time of the hydrogels is closely related to the temperature and the solvents used. The swelling behavior study by gravimetric measurement indicates the hydrogels possess thermosensitivity and exhibit considerable swelling in water. Due to the simplicity of synthesis and no need for initiator or catalyzer and organic solvent, the strategy described here could find a promising application in the preparation of hydrogels.

D-leucine substituted maleimide derivative as well as preparation method and application thereof

-

Paragraph 0039; 0045, (2018/11/03)

The invention discloses a D-leucine substituted maleimide derivative as well as a preparation method thereof. The method comprises the following steps of synthesizing 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazolyl)pyrazol, then adopting a method for generati

L-leucine-substituted maleimide derivative and preparation method and application thereof

-

Paragraph 0023; 0025; 0045, (2018/11/22)

The invention discloses an L-leucine-substituted maleimide derivative and a preparation method thereof. The preparation method comprises the following steps: firstly synthesizing 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazolyl)pyrazole, and using a method for

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 62212-18-4