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118629-59-7

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  • Pentacyclo[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,2,8,14,20-tetrapentyl-, stereoisomer

    Cas No: 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 articles and documents

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.

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.

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

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.

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