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TETRA-N-PENTYLCALIX[4!RESORCINOLARENE, 97 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118629-59-7

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118629-59-7 Usage

Chemical Properties

BROWN FINE CRYSTALLINE POWDER

Check Digit Verification of cas no

The CAS Registry Mumber 118629-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,2 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118629-59:
(8*1)+(7*1)+(6*8)+(5*6)+(4*2)+(3*9)+(2*5)+(1*9)=147
147 % 10 = 7
So 118629-59-7 is a valid CAS Registry Number.

118629-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,8,14,20-tetrapentylpentacyclo<19.3.1.13,7.19,13.115,19>octacosa-1(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23-dodecaene-4,6,10,12,16,18,22,24-octol

1.2 Other means of identification

Product number -
Other names TETRA-N-PENTYLCALIX[4]RESORCINOLARENE

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:118629-59-7 SDS

118629-59-7Downstream Products

118629-59-7Relevant academic research and scientific papers

Preparation of mono-, di- and trisubstituted resorcinol macrocycles

Cortes-Lopez, Gerardo,Gutierrez Tunstad, Linda M.

, p. 139 - 140 (1998)

The synthesis of four new partially substituted resorcinarene macrocycles by a mixed resorcinol-aldehyde condensation method is described.

Radially Oriented [ n]Cyclo- meta-phenylenes

Castro, Edison,Mirzaei, Saber,Hernández Sánchez, Raúl

, p. 87 - 92 (2021)

Molecular compounds with zigzag carbon nanotube geometries are exceedingly rare. Here we report the synthesis and characterization of carbon-based nanotubes with zigzag geometry, best described as radially oriented [n]cyclo-meta-phenylenes, extending the tubularene family of compounds. By the incorporation of edge-sharing benzene rings into the tubularene's radial π-surface, we have uncovered the first step to give rise to the emergence of radial orbital distribution in zigzag nanorings.

C-pentyltetra(3-pyridyl)cavitand: A versatile building block for the directed assembly of hydrogen-bonded heterodimeric capsules

Aakeroey, Christer B.,Schultheiss, Nate,Desper, John

, p. 2607 - 2610 (2006)

Hydrogen-bond-directed assembly of heterodimeric cavitand-based capsules is of considerable interest. Herein, we report the synthesis and single-crystal X-ray structure determination of a pyridyl-functionalized cavitand that contains suitable hydrogen-bond acceptor moieties for the construction of asymmetric cavitand-based capsules.

DISTAL Dibromoresorcin[4]arenes Through Selective Deactivation: A Practical Optimization

Danielsiek, Dominic,Dyker, Gerald

supporting information, p. 6570 - 6575 (2020/11/16)

A simple and straightforward regioselective synthesis of distal disubstituted resorcin[4]arenes was developed, avoiding competing substitution patterns at an early stage via regioselective deactivation. Product limiting reaction steps were optimized by st

A reactive and environmentally friendly protocol for expeditious synthesis of various resorcinarenes using zinc hydrogen sulfate

Mouradzadegun, Arash,Ganjali, Mohammad Reza,Kheirandish, Neda,Abadast, Fatemeh

, p. 377 - 381 (2019/04/03)

In this work, for the first time, metal hydrogen phosphates and sulfates have been studied as effective solid acid catalysts for the condensation of resorcinol with aromatic and aliphatic aldehydes to give tetrameric cyclic products, resorcinarenes, which

Calixarene-mediated liquid-membrane transport of choline conjugates

Adhikari, Birendra Babu,Fujii, Ayu,Schramm, Michael P.

supporting information, p. 2972 - 2979 (2014/05/20)

A series of supramolecular calixarenes efficiently transport distinct molecular species through a liquid membrane when attached to a receptor-complementary choline handle. Calix[6]arene hexacarboxylic acid was highly effective at transporting different target molecules against a pH gradient. Both carboxylic-and phosphonic-acid-functionalized calix[4]arenes effect transport without requiring a pH or ion gradient. NMR binding studies, two-phase solvent extraction, and three-phase transport experiments reveal the necessary and subtle parameters to effect the transport of molecules attached to a choline "handle". On the other hand, rescorin[4]arene cavitands, which have similar guest recognition profiles, did not transport guest molecules. These developments reveal new approaches towards attempting synthetic-receptor-mediated selective small-molecule transport in vesicular and cellular systems.

Towards allosteric receptors - Synthesis of Resorcinarene-Functionalized 2,2′-Bipyridines and their metal complexes

Staats, Holger,Eggers, Friederike,Hass, Oliver,Fahrenkrug, Frank,Matthey, Jens,Luening, Ulrich,Luetzen, Arne

scheme or table, p. 4777 - 4792 (2009/12/25)

Based on a first: example of an allosteric hemicarcerand (1) we prepared four new 2,2′bipyridines that carry resorcinarene moieties in a highly convergent manner. Upon coordination to suitable transition metal ions or their complexes these compounds undergo conformational changes in a way that: they switch between "open" and. "closed" forms (2, 3, and 4) or vice versa (5), thus, bringing together or separating the two functional, moieties on the central, bipyridine, Among the transition metal complexes that act: as effectors for the conformational switching, [Re(CO)5Cl] and monomeric copper(I) complexes of sterically hindered 2,9-arylated 1,10-phenanthrolines proved, to be very effective.

REAGENTS AND METHODS FOR CROSS-LINKING BIOLOGICAL MOLECULES

-

Page/Page column 60-61, (2010/11/28)

The invention provides novel reagents based on calixarene and particularly resorcinarene scaffolds. The reagents are useful as cross-linking reagents for investigating non-covalent interactions between biological macromolecules . Methods of using the nove

Microwave-assisted synthesis of calix[4]resorcinarenes

Hedidi, Madani,Hamdi, Safouane M.,Mazari, Tassadit,Boutemeur, Baya,Rabia, Cherifa,Chemat, Farid,Hamdi, Maamar

, p. 5652 - 5655 (2007/10/03)

Microwave-assisted synthesis of calix[4]resorcinarenes by cyclocondensation of various aldehydes and resorcinol catalysed by 12-tungstophosphoric acid type Keggin (H3PW12O40·13H2O) or concentrated HCl is describ

Bismuth compounds in organic synthesis. Synthesis of resorcinarenes using bismuth triflate

Peterson, Katherine E.,Smith, Russell C.,Mohan, Ram S.

, p. 7723 - 7725 (2007/10/03)

Bismuth triflate (5 mol%) smoothly catalyzes the condensation of aromatic and aliphatic aldehydes with resorcinol to give tetrameric cyclic products, resorcinarenes. With benzaldehyde, the product is obtained as a mixture of two diastereomers and the rati

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