Welcome to LookChem.com Sign In|Join Free
  • or
2,3-(4-Methoxycarbonylbenzo)-1,4,7,10,13-pentaoxacyclopentadec-2-ene is a complex chemical compound characterized by the presence of a benzene ring with a methoxycarbonyl group at the 4-position and a pentaoxacyclopentadec-2-ene ring system. Its unique structure likely imparts distinctive chemical properties, making it a candidate for applications in organic synthesis or material science.

56683-56-8

Post Buying Request

56683-56-8 Suppliers

Recommended suppliers

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

56683-56-8 Usage

Uses

Used in Organic Synthesis:
2,3-(4-Methoxycarbonylbenzo)-1,4,7,10,13-pentaoxacyclopentadec-2-ene is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for the formation of new chemical bonds and the synthesis of novel compounds with potential applications in various fields.
Used in Material Science:
In the field of material science, 2,3-(4-Methoxycarbonylbenzo)-1,4,7,10,13-pentaoxacyclopentadec-2-ene is used as a component in the development of new materials with specific properties. Its incorporation into polymers, for example, may lead to materials with enhanced characteristics such as improved stability, reactivity, or selectivity in certain applications.

Check Digit Verification of cas no

The CAS Registry Mumber 56683-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56683-56:
(7*5)+(6*6)+(5*6)+(4*8)+(3*3)+(2*5)+(1*6)=158
158 % 10 = 8
So 56683-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O7/c1-18-16(17)13-2-3-14-15(12-13)23-11-9-21-7-5-19-4-6-20-8-10-22-14/h2-3,12H,4-11H2,1H3

56683-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-Methoxycarbonylbenzo-15-crown 5-Ether

1.2 Other means of identification

Product number -
Other names methyl 2,5,8,11,14-pentaoxabicyclo[13.4.0]nonadeca-1(15),16,18-triene-17-carboxylate

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:56683-56-8 SDS

56683-56-8Relevant academic research and scientific papers

Combinatorial Evolution of Fast-Conducting Highly Selective K+-Channels via Modularly Tunable Directional Assembly of Crown Ethers

Ren, Changliang,Shen, Jie,Zeng, Huaqiang

supporting information, p. 12338 - 12341 (2017/09/23)

We describe here a modularly tunable molecular strategy for construction and combinatorial optimization of highly efficient K+-selective channels. In our strategy, a highly robust supramolecular H-bonded 1D ensemble was used to order the appended crown ethers in such a way that they roughly stack on top of each other to form a channel for facilitated ion transport across the membrane. Among 15 channels that all prefer K+ over Na+ ions, channel molecule 5F8 shows the most pronounced optimum for K+ while disfavoring all other biologically important cations (e.g., Na+, Ca2+ and Mg2+). With a K+/Na+ selectivity of 9.8 and an EC50 value of 6.2 μM for K+ ion, 5F8 is clearly among the best synthetic potassium channels developed over the past decades.

Syntheses of cis- and trans-dibenzo-30-crown-10 derivatives via regioselective routes and their complexations with paraquat and diquat

He, Chunlin,Shi, Zuming,Zhou, Qizhong,Li, Shijun,Li, Ning,Huang, Feihe

, p. 5872 - 5880 (2008/12/21)

(Chemical Equation Presented) cis-Dibenzo-30-crown-10 (cis-DB30C10) diester and trans-dibenzo-30-crown-10 (trans-DB30C10) diester were synthesized regioselectively with reasonable yields. These two isomers were further reduced to cis-dibenzo-30-crown-10 d

Benzo-15-crown-5 Derivatives. Synthesis and Properies as Ion-extraction and Ion-transport Agents

Haines, Alan H.,Hodgkisson, Ian,Smith, Christopher

, p. 311 - 318 (2007/10/02)

The preparation of some derivatives of benzo-15-crown-5 is described, each containing a carbohydrate moiety attached through either an ester or an ether linkage.The ion-extraction properties into dichloromethane of these and other related benzo-15-crown-5

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 56683-56-8