Welcome to LookChem.com Sign In|Join Free
  • or
N-benzyl-N2-(butylcarbamoyl)-N2-(1-methylethyl)-N-[(5-methylthiophen-2-yl)methyl]glycinamide is a complex organic compound with a molecular formula of C22H32N2O2S. It is a derivative of glycinamide, featuring a benzyl group at the nitrogen atom, a butylcarbamoyl group at the second nitrogen, an isopropyl group at the second nitrogen, and a 5-methylthiophen-2-ylmethyl group at the nitrogen atom. N-benzyl-N~2~-(butylcarbamoyl)-N~2~-(1-methylethyl)-N-[(5-methylthiophen-2-yl)methyl]glycinamide is characterized by its unique structure, which includes a thiophen ring and a glycinamide backbone, and is known for its potential applications in pharmaceuticals and chemical research. The compound's specific properties and reactivity are influenced by the presence of these functional groups, making it a subject of interest for synthetic chemists and researchers in the field of medicinal chemistry.

5918-66-1

Post Buying Request

5918-66-1 Suppliers

Recommended suppliers

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

5918-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5918-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5918-66:
(6*5)+(5*9)+(4*1)+(3*8)+(2*6)+(1*6)=121
121 % 10 = 1
So 5918-66-1 is a valid CAS Registry Number.

5918-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-[butylcarbamoyl(propan-2-yl)amino]-N-[(5-methylthiophen-2-yl)methyl]acetamide

1.2 Other means of identification

Product number -
Other names N-<Indolyl-(3)-methylen>-2-hydroxyanilin

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:5918-66-1 SDS

5918-66-1Downstream Products

5918-66-1Relevant academic research and scientific papers

Ultrasound-assisted synthesis, anticonvulsant activity, and docking study of indole-appended thiazolidin-4-ones

Nikalje, Anna Pratima G.,Shaikh, Sameer I.,Mulay, Abhineet,Khan, Firoz A. K.,Sangshetti, Jaiprakash N.,Shaikh, Shoaib

, p. 756 - 767 (2016/02/26)

Two series of novel indolyl thiazolidin-4-one derivatives 4a-j and 5a-j were obtained by an ecofriendly synthetic protocol by treating a mixture of Schiff's bases (0.01 mol) with thioglycolic acid or thiolactic acid (0.01 mol) and anhydrous zinc chloride

Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde

Sinha, Deepa,Tiwari, Anjani K.,Singh, Sweta,Shukla, Gauri,Mishra, Pushpa,Chandra, Harish,Mishra, Anil K.

, p. 160 - 165 (2008/09/17)

Eight novel heterocyclic Schiff bases derived from the condensation reactions of indole 3-carboxaldehyde with different l-amino acids (histidine, glutamic acid, aspartic acid, leucine, valine) as well as with some aminophenols, have been synthesized and characterized by various spectroscopic methods (IR, MS, 1H NMR). Schiff base derivatives of indole 3-carboxaldehyde were labeled with 99mTc and radiochemical purity was above 97% which is ascertained by instant thin layer chromatography using different solvent conditions. Stability studies of all the derivatives of indole 3-carboxaldehyde was determined under physiological conditions and were stable for more than 24 h. Blood clearance showed a quick wash out from the circulation and biological half life was found to be t1/2(F) = 1 h 15 min; t1/2(S) = 10 h 05 min. Excellent quality radioimages of tumor bearing mice were recorded showing rapid clearance of background activity, visualization of tumor at 3 h and clearance from kidneys of histidine analogue which was further evidenced in biodistribution studies. Antimicrobial activity of these Schiff base compounds was evaluated against Bacillus subtilis, Pseudomonas fluorescence, Staphylococcus aureus, Aspergillus niger, Candida albicans and Trichophyton rubrum.

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 5918-66-1