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Benzaldehyde, 2,2'-[methylenebis(oxy)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77354-97-3

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77354-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77354-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,5 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77354-97:
(7*7)+(6*7)+(5*3)+(4*5)+(3*4)+(2*9)+(1*7)=163
163 % 10 = 3
So 77354-97-3 is a valid CAS Registry Number.

77354-97-3SDS

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 2-[(2-formylphenoxy)methoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names 2,2'-Methandiyldioxy-di-benzaldehyd

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:77354-97-3 SDS

77354-97-3Relevant academic research and scientific papers

Synthesis, characterization and photocatalytic studies of mesoporous silica grafted Ni(ii) and Cu(ii) complexes

Ramanjaneya Reddy,Balasubramanian

, p. 53979 - 53987 (2015)

Mesoporous silica grafted nickel(ii) and copper(ii) complexes of a Schiff base ligand were synthesized. Functionalization of the ligand was achieved by Schiff base condensation of 3-APTES and O,O′-mono methylene bis(salicylidene). The Schiff base moiety w

Synthesis, antitumor activity, enzyme assay, DNA binding and molecular docking of Bis-Schiff bases of pyrazoles

Morsy, Nesrin M.,Hassan, Ashraf S.,Hafez, Taghrid S.,Mahran, Mohamed R. H.,Sadawe, Inass A.,Gbaj, Abdul M.

, p. 47 - 59 (2020/07/27)

A novel series of Bis-Schiff bases of pyrazoles 9–24 were synthesized by the direct condensation of 5-aminopyrazoles 4a–d with dialdehydes 8a–d in ethanol. The newly synthesized Bis-Schiff bases of pyrazoles 9–24 were characterized and confirmed by analyt

Structures of NHC Hg(II) and Ag(I) complexes and selective recognition of nitrate anion

Liu, Qing-Xiang,Zhao, Zhi-Xiang,Zhao, Xiao-Jun,Wei, Qing,Chen, Ai-Hui,Li, Hui-Long,Wang, Xiu-Guang

, p. 1358 - 1373 (2015/02/19)

A series of bis-benzimidazolium (or bis-imidazolium) salts, and their eight N-heterocyclic carbene mercury(II) and silver(I) complexes (1-8) have been synthesized and characterized. Complexes 1-4 and 6 contain similar macrometallocycles formed via one bid

Design and synthesis of rhodamine based chemosensors for the detection of Fe3+ ions

Chereddy, Narendra Reddy,Suman, Koorathota,Thennarasu, Sathiah,Korrapati, Purna Sai,Mandal, Asit Baran

, p. 606 - 613,8 (2020/07/30)

The number and nature of coordinating entities as well as the size of chelating cavity in rhodamine based chemosensors were tuned to enhance the selectivity and sensitivity for Fe3+ ions. An intense pink color development and enhancement in flu

Rhodium(II)-catalyzed cyclization of bis(N-tosylhydrazone)s: An efficient approach towards polycyclic aromatic compounds

Xia, Ying,Liu, Zhenxing,Xiao, Qing,Qu, Peiyuan,Ge, Rui,Zhang, Yan,Wang, Jianbo

supporting information; experimental part, p. 5714 - 5717 (2012/07/28)

Ahead of the PAC: Polycyclic aromatic compounds (PACs) can be easily accessed by the combination of Suzuki-Miyaura cross-coupling and a [Rh 2(OAc)4]-catalyzed carbene reaction using easily available bis(N-tosylhydrazone)s as intermediates (see scheme; Ts=4-toluenesulfonyl). Copyright

Synthesis, physico-chemical, structure and supramolecular properties of pinacolophanes: Versatile synthetic precursors to stilbenophanes

Darabi, Hossein Reza,Karouei, Mohammad Hashemi,Tehrani, Mohammad Jafar,Aghapoor, Kiomars,Ghasemzadeh, Mitra,Neumueller, Bernhard

body text, p. 462 - 469 (2012/01/13)

Novel pinacolophanes tethered by methyl and ethyl chains were synthesised and characterised. The stereochemistry of these small-sized cyclophanes was determined by NMR spectral data as well as by single-crystal X-ray analysis. Intramolecular hydrogen bond

Synthesis of imines, diimines and macrocyclic diimines as possible ligands, in aqueous solution

Simion, Alina,Simion, Cristian,Kanda, Tadeshige,Nagashima, Satoko,Mitoma, Yoshiharu,Yamada, Tomoko,Mimura, Keisuke,Tashiro, Masashi

, p. 2071 - 2078 (2007/10/03)

Although it is recognized that the presence of water is disadvantageous for imine synthesis, we demonstrate that such synthesis can be effective in completely aqueous media, without any catalyst and under mild conditions. Thus, arylaryl, aryl-alkyl, alkyl-aryl and alkyl-alkyl monoimines as well as a large variety of diimines are obtained by direct condensation of the corresponding carbonyl compounds and amines, in water. The same process is used to synthesize macrocyclic diimines starting from methylene, ethylene, trimethylene and tetramethylene glycol bis(2-formylphenyl ether) and ethylene-, trimethylene- and tetramethylene-diamine, some of these macrocycles being known for their chelating properties.

Synthesis of new dihydroxy-dioxygenated ortho-[2,x]cyclophanes

Simion, Cristian,Simion, Alina,Mitoma, Yoshiharu,Nagashima, Satoko,Kawaji, Takatoshi,Hashimoto, Iwao,Tashiro, Masashi

, p. 2459 - 2470 (2007/10/03)

The synthesis of title compounds (1a-f) by intramolecular reductive coupling is presented. The reaction is carried out in water solution, in the presence of Zn or Al powder, in basic media.

Design, Synthesis, and Structure-Activity Relationship Studies for a New Imidazole Series of J774 Macrophage Specific Acyl-CoA:Cholesterol Acyltransferase (ACAT) Inhibitors

Maduskuie, Thomas P.,Wilde, Richard G.,Billheimer, Jeffrey T.,Cromley, Debra A.,Germain, Sandra,et al.

, p. 1067 - 1083 (2007/10/02)

Acyl-CoA:cholesterol acyltransferase (ACAT) is the primary enzyme involved in intracellular cholesterol esterification.Arterial wall infiltration by macrophages and subsequent uncontrolled esterification of cholesterol leading to foam cell formation is believed to be an important process which leads to the development of fatty streaks.Inhibitors of the ACAT enzyme may retard this atherogenic process.We have recently discovered a series of imidazoles which are potent in vitro ACAT inhibitors in the J774 macrophage cell culture assay.This paper will describe the design, synthesis, and structure-activity relationship for this very potent series of compounds.

New Macrocyclic Ligands. Synthesis of an Extensive Series of Potentially Pentadentate Ligands Containing Mixed Nitrogen, Oxygen and/or Sulfur Heteroatoms. The X-Ray Structure of an O2N2S Derivative

Baldwin, Darren,Duckworth, Paul A.,Erickson, Gary R.,Lindoy, Leonard F.,McPartlin, Mary,et al.

, p. 1861 - 1872 (2007/10/02)

The syntheses of 16 new 16- to 19-membered dibenzo macrocycles are reported.These rings incorporate nitrogen together with oxygen and/or sulfur heteroatoms.The X-ray structure of the 17-membered macrocycle containing an O2N2S heteroatom set is described.

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