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Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184587-74-4

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184587-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184587-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,5,8 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 184587-74:
(8*1)+(7*8)+(6*4)+(5*5)+(4*8)+(3*7)+(2*7)+(1*4)=184
184 % 10 = 4
So 184587-74-4 is a valid CAS Registry Number.

184587-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[3,5-bis[(2-formylphenoxy)methyl]phenyl]methoxy]benzaldehyde

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:184587-74-4 SDS

184587-74-4Downstream Products

184587-74-4Relevant academic research and scientific papers

A hemicryptophane with a triple-stranded helical structure

Long, Augustin,Perraud, Olivier,Jeanneau, Erwann,Aronica, Christophe,Dutasta, Jean-Pierre,Martinez, Alexandre

, p. 1885 - 1889 (2018)

A hemicryptophane cage bearing amine and amide functions in its three linkers was synthesized in five steps. The X-ray molecular structure of the cage shows a triple-stranded helical arrangement of the linkers stabilized by intramolecular hydrogen bonds b

Size mismatch between two tripodal units: A new synthetic strategy for macrotricyclic cryptand

Chand, Dillip K.,Bharadwaj, Parimal K.

, p. 8443 - 8446 (1996)

Tripods of matched/mismatched sizes lead to a macrobicyclic/macrotricyclic cryptand in high yield by Schiff base condensation at 5°C in the absence of any templating metal ion.

Synthesis, characterization, and pH-induced luminescence switching of two trinuclear Ru(II) polypyridyl complexes containing imidazole

Cheng, Feixiang,Chen, Jishu,Wang, Fan,Tang, Ning,Hou, Nengbang,Chen, Guang

, p. 415 - 421 (2012)

Two tripodal ligands H3L1 and H3L 2 containing imidazole rings have been prepared by the reaction of 1,10- phenanthroline-5,6-dione with 1,3,5-tris[(4-formylphenoxy)- methyl]benzene and 1,3,5-tris[(2-formylpheno

Helical Chirality Induces a Substrate-Selectivity Switch in Carbohydrates Recognitions

Long, Augustin,Perraud, Olivier,Albalat, Muriel,Robert, Vincent,Dutasta, Jean-Pierre,Martinez, Alexandre

, p. 6301 - 6306 (2018)

A new chiral hemicryptophane cage combining an electron-rich cyclotriveratrylene (CTV) unit and polar amine functions has been synthesized. The resolution of the racemic mixture has been performed by chiral HPLC, and the assignment of the absolute configu

Synthesis and Structures of Novel Multi-armed Molecules Involving Benzene as a Core and 4-Phenylthiazole, 4-Pyrazolylthiazole, or Thiadiazole Units as Arms

Salem, Mostafa E.,Darweesh, Ahmed F.,Farag, Ahmad M.,Elwahy, Ahmed H. M.

, p. 586 - 595 (2017/02/03)

A synthesis of novel three-, four-, and sixfold branched 4-phenylthiazolylhydrazones, 4-pyrazolylthiazolyl hydrazones, and thiadiazoles which are linked to a benzene core via phenoxymethyl spacers was reported. The synthetic methodology includes initially formation of poly(aldehyde thiosemicarbazones) 9, 14, and 15 by acid catalyzed condensation of thiosemicarbazide (8) with the appropriate poly(aldehydes) 3, 5, and 7, respectively. Subsequent reaction of 9, 14, and 15 with each of 2-bromo-1-phenylethanone (10a) and 2-bromo-1-(4-chlorophenyl)ethanone (10b) in refluxing ethanol in the presence of few drops of TEA afforded 11, 16, and 18, respectively, in good yields. On the other hand, the synthesis of the novel poly(4,5-dihydro-1,3,4-thiadiazolyl) derivatives 20, 21a,21b, and 22 was performed by cyclization of 9b, 14a,14b, and 15a, respectively, in refluxing acetic anhydride.

Efficient synthesis and host-guest properties of a new class of calix[6]azacryptands

Le Gac, Stephane,Zeng, Xianshun,Girardot, Camille,Jabin, Ivan

, p. 9233 - 9236 (2007/10/03)

(Chemical Equation Presented) Two members of a new class of calix[6]azacryptands, namely, calix[6]tampo and calix[6]tamb, have been synthesized through an efficient [1 + 1] macrocyclization reaction - reduction sequence. One of them has been obtained in a

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