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1-[2-(morpholin-4-yl)ethyl]-3-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83935-71-1

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83935-71-1 Usage

Molecular structure

The compound has a complex molecular structure, consisting of a urea group, a morpholine ring, and a cyclopentadecin ring with multiple oxygen atoms.

Functional groups

The compound contains a urea group (-NH2-CO-NH2) and a morpholine ring (a six-membered heterocyclic ring containing two nitrogen atoms and one oxygen atom).

Hydrogen bonding

The urea group in the compound can participate in hydrogen bonding, which may contribute to its biological activity and interactions with other molecules.

Solubility

The compound is likely to be soluble in polar solvents such as water and methanol due to the presence of polar functional groups like the urea group and the oxygen atoms in the morpholine and cyclopentadecin rings.

Potential applications

The compound has potential applications in medicinal chemistry, particularly in the development of new pharmaceuticals. Its unique structure suggests that it may have biological activity and could potentially be used as a drug or as a chemical intermediate in the synthesis of bioactive compounds.

Further research

The compound's properties and potential uses warrant further exploration and research to better understand its biological activity, pharmacological properties, and potential applications in drug development.

Safety and toxicity

The safety and toxicity of the compound are not known and would need to be evaluated through appropriate testing and research.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, light exposure) is not known and would need to be determined through further research.

Synthesis

The synthesis of the compound may involve multiple steps, including the formation of the urea group, the morpholine ring, and the cyclopentadecin ring, as well as the introduction of the oxygen atoms. The specific synthetic route and reaction conditions would need to be optimized for efficient and scalable production.

Check Digit Verification of cas no

The CAS Registry Mumber 83935-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83935-71:
(7*8)+(6*3)+(5*9)+(4*3)+(3*5)+(2*7)+(1*1)=161
161 % 10 = 1
So 83935-71-1 is a valid CAS Registry Number.

83935-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-morpholin-4-ylethyl)-3-(2,5,8,11,14-pentaoxabicyclo[13.4.0]nonadeca-1(15),16,18-trien-17-yl)urea

1.2 Other means of identification

Product number -
Other names -

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:83935-71-1 SDS

83935-71-1Downstream Products

83935-71-1Relevant academic research and scientific papers

Benzocrown Derivatives as Ionophores for Alkali Cations, I. - Synthesis of Urethane- and Urea-Linked Mono- and Bis-Crown Ethers

Toeke, Laszlo,Bitter, Istvan,Agai, Bela,Csongor, Eva,Toth, Klara,et al.

, p. 349 - 354 (2007/10/02)

New mono- and bis-benzocrown ethers (5-28 and 29-48) with different substituents and connecting chains were prepared with the aim to develop novel alkali cation-transport mediators for biological systems.The alkali cation selectivities of the title compounds were determined in ion-selective membrane electrodes.Remarkable potassium selectivity was observed with several bis(benzo-15-crown-5)urethanes.

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