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Pentalamide is a synthetic chemical compound, specifically a pentapeptide, which consists of five amino acid residues linked by peptide bonds. It is known for its potential applications in various fields, including pharmaceuticals and cosmetics, due to its ability to mimic the effects of certain natural peptides. Pentalamide is often used in the development of drugs targeting specific receptors or as a component in skincare products to promote healing and regeneration. Its unique structure allows for a range of biological activities, making it a subject of interest for researchers exploring its therapeutic potential.

5579-06-6

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5579-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5579-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5579-06:
(6*5)+(5*5)+(4*7)+(3*9)+(2*0)+(1*6)=116
116 % 10 = 6
So 5579-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-2-3-6-9-15-11-8-5-4-7-10(11)12(13)14/h4-5,7-8H,2-3,6,9H2,1H3,(H2,13,14)

5579-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pentoxybenzamide

1.2 Other means of identification

Product number -
Other names Pentalamide

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:5579-06-6 SDS

5579-06-6Relevant academic research and scientific papers

Copper-Catalyzed Self-Condensation of Benzamide: Domino Reactions towards Quinazolinones

Sayyad, Nisar,Cele, Zamani,Aleti, Rajeshwar Reddy,Bera, Milan,Cherukupalli, Srinivasulu,Chandrasekaran, Balakumar,Kushwaha, Narva Deshwar,Karpoormath, Rajshekhar

supporting information, p. 5382 - 5388 (2018/10/20)

We herein report a simple and highly efficient microwave-assisted, copper-catalyzed and ligand-free synthetic method for 2-substituted 4(3H)-quinazolinones as domino reaction. This reaction proceeds via self-condensation of substrate (2-bromo/iodo benzamide) in the presence of a strong base and copper catalyst. The substituted quinazolinones were obtained in one-pot reaction by intramolecular cyclization (condensation) via Ullmann–type intermediate. Both the intermediates and quinazolinones were obtained in good yield and can be further used as building blocks for developing the potential novel drug-like compounds.

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