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1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 259748-16-8 Structure
  • Basic information

    1. Product Name: 1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane
    2. Synonyms: 1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane
    3. CAS NO:259748-16-8
    4. Molecular Formula:
    5. Molecular Weight: 356.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 259748-16-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane(259748-16-8)
    11. EPA Substance Registry System: 1,2-bis(2-hydroxy-4-methoxy-α-methylbenzylideneimino)ethane(259748-16-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 259748-16-8(Hazardous Substances Data)

259748-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259748-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,7,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 259748-16:
(8*2)+(7*5)+(6*9)+(5*7)+(4*4)+(3*8)+(2*1)+(1*6)=188
188 % 10 = 8
So 259748-16-8 is a valid CAS Registry Number.

259748-16-8Downstream Products

259748-16-8Relevant articles and documents

Syntheses, hydrogen-bonded assembly structures, and spin crossover properties of [FeIII(Him)2(n-MeOhapen)]PF6 (Him = imidazole and n-MeOhapen = N,N′-bis(n-methoxy-2-oxyacetophenylidene)ethylenediamine); n = 4, 5, 6)

Fujinami, Takeshi,Ikeda, Mizuki,Koike, Masataka,Matsumoto, Naohide,Oishi, Tomohiro,Sunatsuki, Yukinari

, p. 89 - 95 (2015)

Three iron(III) complexes, [FeIII(Him)2(n-MeOhapen)]PF6 (1: n = 4, 2: n = 5, 3: n = 6), where Him = imidazole and n-MeOhapen = N,N′-bis(n-methoxy-2-oxyacetophenylidene)ethylenediamine, were synthesized. Each FeIII/su

Synthesis, hydrogen-bonded 1D structure, and abrupt spin transition between high-spin (HS) and an ordered [HS-HS-HS-LS] of a mononuclear iron(III) complex [FeIII(Him)2(4-MeOhapen)]CF3SO3 (Him = imidazole, 4-MeOh

Miyano, Kyohei,Nishida, Takahiro,Ono, Hiromasa,Hamada, Daisuke,Fujinami, Takeshi,Matsumoto, Naohide,Sunatsuki, Yukinari

, p. 49 - 54 (2016)

A SCO iron(III) complex [FeIII(Him)2(4MeOhapen)]CF3SO3 was synthesized, where Him = imidazole and 4-MeOhapen = N,N′-bis(2-oxy-4-methoxyacetophenylidene)ethylenediamine. FeIII ion has an octahedral coo

Low-dose paeonol derivatives alleviate lipid accumulation

Pao, Kuan-Chuan,Zhao, Jin-Feng,Lee, Tzong-Shyuan,Huang, Ying-Pei,Han, Chien-Chung,Sherlock Huang, Lin-Chiang,Wu, Kou-Hung,Hsu, Ming-Hua

, p. 5652 - 5656 (2015/03/04)

Here, we present a series of novel paeonol derivatives that prevent lipid accumulation at lower doses and exhibit improved water solubility. According to SAR analysis results, 1-(4-methoxy-2-(2-(piperidin-1-yl)ethoxy)phenyl)ethanone (6a) and 4′-methoxy-2′

Evaluation of the antioxidant, DNA interaction and tumor cell cytotoxicity activities of Copper(II) complexes with Paeonol Schiff-base

Qin, Dong-Dong,Yang, Zheng-Yin,Zhang, Fu-Hong,Du, Bo,Wang, Ping,Li, Tian-Rong

body text, p. 727 - 729 (2010/10/01)

Herein, we report for the first time on the preparation of four Paeonol Schiff-base ligands: 1,2-Bis(2- hydroxy-4-methoxy-a-methylbenzylideneimino) ethane (H2L1), 2-hydroxy-4-methoxy-α- methylbenzylidene (benzoyl) hydrazone (HL2

New compounds of tetradentate Schiff bases with vanadium(IV) and vanadium(V)

Choudhary, Nosheen F.,Connelly, Neil G.,Hitchcock, Peter B.,Leigh, G. Jeffery

, p. 4437 - 4446 (2007/10/03)

A new range of potentially tetradentate proligands, H2L, derived from aromatic aldehydes and ketones and aliphatic diamines has been prepared. Their vanadyl(IV) and vanadyl(V) complexes [VO(L)] and [VO(L)]+, and also some adducts [VO(L)→VO(L)]+, have been synthesized. The structures of four selected complexes have been determined and it is shown that these must be a result of both steric and electronic factors that make prediction of conformation and stacking difficult. The adducts [VO(L)→VO(L)]+ have structures that persist in solution in dichloromethane, where they can undergo redox chemistry, but they apparently dissociate into their component complexes in the donor solvent acetonitrile. The Royal Society of Chemistry 1999.

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